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<title>Chemotherapy Updates</title>
<link>https://updates.chemo.org.uk/#category=News</link>
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<lastBuildDate>Tue, 08 Sep 2026 23:09:20 GMT</lastBuildDate>
<item>
  <title>UK SACT Board Consent Forms</title>
  <link>https://updates.chemo.org.uk/news/ConsentNews_-Inf.html</link>
  <description><![CDATA[ 




<div class="cell">
<div class="cell-output cell-output-stderr">
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<p>The standardised UK SACT Consent Forms which are hosted on the <a href="https://www.cancerresearchuk.org/health-professional/treatment-and-other-post-diagnosis-issues/consent-forms-for-sact-systemic-anti-cancer-therapy">CRUK Website</a> have been updated.</p>
<p>According to the CRUK Webpage, the latest updates took place on -Inf and made the following updates:</p>
<ul>
<li></li>
</ul>



 ]]></description>
  <category>News</category>
  <category>Consent</category>
  <guid>https://updates.chemo.org.uk/news/ConsentNews_-Inf.html</guid>
  <pubDate>Tue, 08 Sep 2026 23:09:20 GMT</pubDate>
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</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.406.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.406) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 6, August 2026.</p>
<p>The following changes have been introduced:</p>
<section id="acalabrutinib-in-combination-bendamustine-and-rituximab-aca4" class="level2">
<h2 class="anchored" data-anchor-id="acalabrutinib-in-combination-bendamustine-and-rituximab-aca4">Acalabrutinib in combination bendamustine and rituximab (<a href="../CDF_Forms/ACA4.html">ACA4</a>)</h2>
<p>Acalabrutinib in combination with bendamustine and rituximab for UNTREATED mantle cell lymphoma when an autologous stem cell transplant is UNSUITABLE where the following <a href="../CDF_Forms/ACA4.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="acalabrutinib-in-combination-with-venetoclax-aca5" class="level2">
<h2 class="anchored" data-anchor-id="acalabrutinib-in-combination-with-venetoclax-aca5">Acalabrutinib in combination with venetoclax (<a href="../CDF_Forms/ACA5.html">ACA5</a>)</h2>
<p>Acalabrutinib in combination with venetoclax for the 1st line treatment of previously untreated chronic lymphocytic leukaemia where the following <a href="../CDF_Forms/ACA5.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="gilteritinib-gilt2" class="level2">
<h2 class="anchored" data-anchor-id="gilteritinib-gilt2">Gilteritinib (<a href="../CDF_Forms/GILT2.html">GILT2</a>)</h2>
<p>For the treatment of relapsed/refractory FLT3 mutation positive acute myeloid leukaemia in POST PUBESCENT CHILDREN where the following <a href="../CDF_Forms/GILT2.html">criteria</a> have been met</p>
<p><strong>Medicines For Children form created for TA642</strong></p>
</section>
<section id="na-nhse-policy-2268" class="level2">
<h2 class="anchored" data-anchor-id="na-nhse-policy-2268">NA (<a href="../CDF_Forms/NHSE Policy 2268.html">NHSE Policy 2268</a>)</h2>
<p>NA</p>
<p><strong>Clinicial Commissioning Policy: added directly into routine commissioning - section B of list</strong></p>
</section>
<section id="na-nhse-policy-2432" class="level2">
<h2 class="anchored" data-anchor-id="na-nhse-policy-2432">NA (<a href="../CDF_Forms/NHSE Policy 2432.html">NHSE Policy 2432</a>)</h2>
<p>NA</p>
<p><strong>Clinicial Commissioning Policy: added directly into routine commissioning - section B of list</strong></p>
</section>
<section id="belantamab-mafodotin-in-combination-with-bortezomib-and-dexamethasone-bela1" class="level2">
<h2 class="anchored" data-anchor-id="belantamab-mafodotin-in-combination-with-bortezomib-and-dexamethasone-bela1">Belantamab mafodotin in combination with bortezomib and dexamethasone (<a href="../CDF_Forms/BELA1.html">BELA1</a>)</h2>
<p>Belantamab mafodotin in combination with bortezomib and dexamethasone as 2nd line treatment of relapsed or refractory myeloma in adult patients where the following <a href="../CDF_Forms/BELA1.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="encorafenib-in-combination-with-binimetinib-enc3" class="level2">
<h2 class="anchored" data-anchor-id="encorafenib-in-combination-with-binimetinib-enc3">Encorafenib in combination with binimetinib (<a href="../CDF_Forms/ENC3.html">ENC3</a>)</h2>
<p>For the first line treatment of metastatic BRAF V600 mutation positive non-small cell lung cancer where the following <a href="../CDF_Forms/ENC3.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="pembrolizumab-pemb34" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb34">Pembrolizumab (<a href="../CDF_Forms/PEMB34.html">PEMB34</a>)</h2>
<p>Pembrolizumab for resectable, locally advanced, head and neck squamous cell carcinoma in adults whose tumours express PD-L1 with a combined positive score of 1 or more where the following <a href="../CDF_Forms/PEMB34.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="ripretinib-rip1" class="level2">
<h2 class="anchored" data-anchor-id="ripretinib-rip1">Ripretinib (<a href="../CDF_Forms/RIP1.html">RIP1</a>)</h2>
<p>Ripretinib for treating advanced gastrointestinal stromal tumours after 3 more kinase inhibitors where the following <a href="../CDF_Forms/RIP1.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="vorasidenib-vor1" class="level2">
<h2 class="anchored" data-anchor-id="vorasidenib-vor1">Vorasidenib (<a href="../CDF_Forms/VOR1.html">VOR1</a>)</h2>
<p>For treating astrocytoma or oligodendroglioma with IDH1 or IDH2 mutations after surgery in patients aged 12 years and over where the following <a href="../CDF_Forms/VOR1.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="zanidatamab-zani1" class="level2">
<h2 class="anchored" data-anchor-id="zanidatamab-zani1">Zanidatamab (<a href="../CDF_Forms/ZANI1.html">ZANI1</a>)</h2>
<p>For the treatment of HER2-positive advanced biliary tract cancer after 1 or more lines of systemic treatment where the following <a href="../CDF_Forms/ZANI1.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="amivantamab-in-combination-with-lazertinib-ami1" class="level2">
<h2 class="anchored" data-anchor-id="amivantamab-in-combination-with-lazertinib-ami1">Amivantamab in combination with lazertinib (<a href="../CDF_Forms/AMI1.html">AMI1</a>)</h2>
<p>For the first line treatment of locally advanced or metastatic non-small cell lung cancer in adults whose tumours have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations where the following <a href="../CDF_Forms/AMI1.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 3 and 4) updated</strong></p>
</section>
<section id="dostarlimab-dos1" class="level2">
<h2 class="anchored" data-anchor-id="dostarlimab-dos1">Dostarlimab (<a href="../CDF_Forms/DOS1.html">DOS1</a>)</h2>
<p>Dostarlimab monotherapy for patients with microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) recurrent/advanced endometrial carcinoma after prior platinum-based chemotherapy where the following <a href="../CDF_Forms/DOS1.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 8, 10 and 11) updated</strong></p>
</section>
<section id="inotuzumab-ozogamicin-ino2" class="level2">
<h2 class="anchored" data-anchor-id="inotuzumab-ozogamicin-ino2">Inotuzumab ozogamicin (<a href="../CDF_Forms/INO2.html">INO2</a>)</h2>
<p>The treatment of relapsed/refractory Philadelphia positive and negative B cell precursor acute lymphoblastic leukaemia in CHILD patients where all the following criteria are met:</p>
<p><strong>Treatment criterion (#4, 6, 7 and 10) updated</strong></p>
</section>
<section id="isatuximab-in-combination-with-pomalidomide-and-dexamethasone-isa1" class="level2">
<h2 class="anchored" data-anchor-id="isatuximab-in-combination-with-pomalidomide-and-dexamethasone-isa1">Isatuximab in combination with pomalidomide and dexamethasone (<a href="../CDF_Forms/ISA1.html">ISA1</a>)</h2>
<p>Isatuximab in combination with pomalidomide and dexamethasone for the 4th line treatment of adult patients with relapsed/refractory multiple myeloma where the following <a href="../CDF_Forms/ISA1.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 9 and 14) updated</strong></p>
</section>
<section id="na-niv8" class="level2">
<h2 class="anchored" data-anchor-id="na-niv8">NA (<a href="../CDF_Forms/NIV8.html">NIV8</a>)</h2>
<p>NA</p>
<p><strong>Treatment criterion (#1 and 5) updated</strong></p>
</section>
<section id="nivolumab-and-ipilimumab-niv18" class="level2">
<h2 class="anchored" data-anchor-id="nivolumab-and-ipilimumab-niv18">Nivolumab and ipilimumab (<a href="../CDF_Forms/NIV18.html">NIV18</a>)</h2>
<p>Nivolumab in combination with ipilimumab for treating advanced melanoma</p>
<p><strong>Treatment criterion (#1 and 4) updated</strong></p>
</section>
<section id="nivolumab-in-combination-with-relatlimab-opdualag-nivrel1" class="level2">
<h2 class="anchored" data-anchor-id="nivolumab-in-combination-with-relatlimab-opdualag-nivrel1">Nivolumab in combination with relatlimab (Opdualag ®) (<a href="../CDF_Forms/NIVREL1.html">NIVREL1</a>)</h2>
<p>As first immunotherapy for treating unresectable or metastatic melanoma patients aged 12 years or more where the following <a href="../CDF_Forms/NIVREL1.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 5 and 10) updated</strong></p>
</section>
<section id="pembrolizumab-pemb9a" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb9a">Pembrolizumab (<a href="../CDF_Forms/PEMB9a.html">PEMB9a</a>)</h2>
<p>Pembrolizumab monotherapy for treating unresectable or advanced malignant melanoma (form a): REGISTRATION OF START OF PEMBROLIZUMAB MONOTHERAPY OR OF PREVIOUSLY COMMENCED AND CURRENTLY CONTINUED PEMBROLIZUMAB MONOTHERAPY This form comes in 3 parts. 1. The first part is for patients who are either scheduled to commence pembrolizumab monotherapy or who commenced and continue to receive pembrolizumab monotherapy. 2. The second part of the form which must use the same unique Blueteq identifier is for those benefitting patients who choose to electively discontinue pembrolizumab after 2 or more years of treatment; this second part (patient details be automatically entered) will only appear once the first part of the form is approved and should be completed at the time of elective discontinuation of pembrolizumab. 3. The third part of the form which must use the same unique Blueteq identifier is for those patients registered as having electively and previously stopped pembrolizumab and in whom there is disease progression for which the clinician wishes to re-commence pembrolizumab; this third part of the form (patient details will automatically entered) will only appear once</p>
<p><strong>Treatment criterion (#1 and 5) updated</strong></p>
</section>
<section id="pembrolizumab-pemb16" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb16">Pembrolizumab (<a href="../CDF_Forms/PEMB16.html">PEMB16</a>)</h2>
<p>For relapsed/refractory classical Hodgkin lymphoma in patients aged 3 years and older who have been treated with stem cell transplantation but never previously received brentuximab vedotin where the following <a href="../CDF_Forms/PEMB16.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 8, 10 and 11) updated</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.406.html</guid>
  <pubDate>Wed, 05 Aug 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.405.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.405) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 25, June 2026.</p>
<p>The following changes have been introduced:</p>
<section id="pembrolizumab-with-chemoradiotherapy-pemb36" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-with-chemoradiotherapy-pemb36">Pembrolizumab with chemoradiotherapy (<a href="../CDF_Forms/PEMB36.html">PEMB36</a>)</h2>
<p>Pembrolizumab with chemoradiotherapy for untreated locally advanced cervical cancer where the following <a href="../CDF_Forms/PEMB36.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="daratumumab-in-combination-with-bortezomib-lenalidomide-and-dexamethasone-dar6" class="level2">
<h2 class="anchored" data-anchor-id="daratumumab-in-combination-with-bortezomib-lenalidomide-and-dexamethasone-dar6">Daratumumab in combination (with bortezomib, lenalidomide, and dexamethasone) (<a href="../CDF_Forms/DAR6.html">DAR6</a>)</h2>
<p>For UNTREATED multiple myeloma when a stem cell transplant is UNSUITABLE where the following <a href="../CDF_Forms/DAR6.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="mirvetuximab-soravtansine-mir1" class="level2">
<h2 class="anchored" data-anchor-id="mirvetuximab-soravtansine-mir1">Mirvetuximab soravtansine (<a href="../CDF_Forms/MIR1.html">MIR1</a>)</h2>
<p>For treating folate receptor-alpha-positive platinum-resistant epithelial ovarian, fallopian tube or primary peritoneal cancer where the following <a href="../CDF_Forms/MIR1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.405.html</guid>
  <pubDate>Tue, 30 Jun 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.404.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.404) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Tuesday 23, June 2026.</p>
<p>The following changes have been introduced:</p>
<section id="cemiplimab-cem3" class="level2">
<h2 class="anchored" data-anchor-id="cemiplimab-cem3">Cemiplimab (<a href="../CDF_Forms/CEM3.html">CEM3</a>)</h2>
<p>To treat recurrent or metastatic cervical cancer that has progressed on or after platinum-based chemotherapy where the following <a href="../CDF_Forms/CEM3.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="na-epc2" class="level2">
<h2 class="anchored" data-anchor-id="na-epc2">NA (<a href="../CDF_Forms/EPC2.html">EPC2</a>)</h2>
<p>NA</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="cemiplimab-with-platinum-based-chemotherapy-cem2" class="level2">
<h2 class="anchored" data-anchor-id="cemiplimab-with-platinum-based-chemotherapy-cem2">Cemiplimab with platinum-based chemotherapy (<a href="../CDF_Forms/CEM2.html">CEM2</a>)</h2>
<p>For untreated advanced non-small-cell lung cancer where the following <a href="../CDF_Forms/CEM2.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="serplulimab-in-combination-with-carboplatin-and-etoposide-ser1-serplulimab-in-combination-with-carboplatin-and-etoposide-ser1" class="level2">
<h2 class="anchored" data-anchor-id="serplulimab-in-combination-with-carboplatin-and-etoposide-ser1-serplulimab-in-combination-with-carboplatin-and-etoposide-ser1">Serplulimab in combination with carboplatin and etoposide (<a href="../CDF_Forms/SER1.html">SER1</a>) ## Serplulimab in combination with carboplatin and etoposide (<a href="../CDF_Forms/SER1.html">SER1</a>)</h2>
<p>For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/SER1.html">criteria</a> have been met For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/SER1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated Treatment criteria (#3) updated</strong></p>
</section>
<section id="tisotumab-vedotin-tisv1" class="level2">
<h2 class="anchored" data-anchor-id="tisotumab-vedotin-tisv1">Tisotumab vedotin (<a href="../CDF_Forms/TISV1.html">TISV1</a>)</h2>
<p>For treating recurrent or metastatic cervical cancer that has progressed on or after systemic treatment where the following <a href="../CDF_Forms/TISV1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="atezolizumab-in-combination-with-carboplatin-and-etoposide-ate7" class="level2">
<h2 class="anchored" data-anchor-id="atezolizumab-in-combination-with-carboplatin-and-etoposide-ate7">Atezolizumab in combination with carboplatin and etoposide (<a href="../CDF_Forms/ATE7.html">ATE7</a>)</h2>
<p>For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/ATE7.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 2, 3, 5 and 9) updated; Treatment criterion (#2, 4, 11 and 12) removed</strong></p>
</section>
<section id="daratumumab-in-combination-with-bortezomib-lenalidomide-and-dexamethasone-dar6" class="level2">
<h2 class="anchored" data-anchor-id="daratumumab-in-combination-with-bortezomib-lenalidomide-and-dexamethasone-dar6">Daratumumab in combination (with bortezomib, lenalidomide, and dexamethasone) (<a href="../CDF_Forms/DAR6.html">DAR6</a>)</h2>
<p>For UNTREATED multiple myeloma when a stem cell transplant is UNSUITABLE where the following <a href="../CDF_Forms/DAR6.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#8) updated</strong></p>
</section>
<section id="durvalumab-in-combination-with-etoposide-plus-either-carboplatin-or-cisplatin-dur4" class="level2">
<h2 class="anchored" data-anchor-id="durvalumab-in-combination-with-etoposide-plus-either-carboplatin-or-cisplatin-dur4">Durvalumab in combination with etoposide plus either carboplatin or cisplatin (<a href="../CDF_Forms/DUR4.html">DUR4</a>)</h2>
<p>For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/DUR4.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 2, 3, 5, 6 and 9) updated; Treatment criterion (#2, 4, 8, 12 and 13) removed</strong></p>
</section>
<section id="serplulimab-in-combination-with-carboplatin-and-etoposide-ser1-serplulimab-in-combination-with-carboplatin-and-etoposide-ser1-1" class="level2">
<h2 class="anchored" data-anchor-id="serplulimab-in-combination-with-carboplatin-and-etoposide-ser1-serplulimab-in-combination-with-carboplatin-and-etoposide-ser1-1">Serplulimab in combination with carboplatin and etoposide (<a href="../CDF_Forms/SER1.html">SER1</a>) ## Serplulimab in combination with carboplatin and etoposide (<a href="../CDF_Forms/SER1.html">SER1</a>)</h2>
<p>For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/SER1.html">criteria</a> have been met For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/SER1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated Treatment criteria (#3) updated</strong></p>
</section>
<section id="zanidatamab-zani1" class="level2">
<h2 class="anchored" data-anchor-id="zanidatamab-zani1">Zanidatamab (<a href="../CDF_Forms/ZANI1.html">ZANI1</a>)</h2>
<p>For the treatment of HER2-positive advanced biliary tract cancer after 1 or more lines of systemic treatment where the following <a href="../CDF_Forms/ZANI1.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#2) corrected</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.404.html</guid>
  <pubDate>Sat, 27 Jun 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.403.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.403) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Monday 8, June 2026.</p>
<p>The following changes have been introduced:</p>
<section id="daratumumab-in-combination-with-bortezomib-lenalidomide-and-dexamethasone-dar6" class="level2">
<h2 class="anchored" data-anchor-id="daratumumab-in-combination-with-bortezomib-lenalidomide-and-dexamethasone-dar6">Daratumumab in combination (with bortezomib, lenalidomide, and dexamethasone) (<a href="../CDF_Forms/DAR6.html">DAR6</a>)</h2>
<p>For UNTREATED multiple myeloma when a stem cell transplant is UNSUITABLE where the following <a href="../CDF_Forms/DAR6.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.403.html</guid>
  <pubDate>Sun, 14 Jun 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
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<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.402.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.402) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 4, June 2026.</p>
<p>The following changes have been introduced:</p>
<section id="mirvetuximab-soravtansine-mir1" class="level2">
<h2 class="anchored" data-anchor-id="mirvetuximab-soravtansine-mir1">Mirvetuximab soravtansine (<a href="../CDF_Forms/MIR1.html">MIR1</a>)</h2>
<p>For treating folate receptor-alpha-positive platinum-resistant epithelial ovarian, fallopian tube or primary peritoneal cancer where the following <a href="../CDF_Forms/MIR1.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="durvalumab-with-gemcitabine-and-cisplatin-dur8" class="level2">
<h2 class="anchored" data-anchor-id="durvalumab-with-gemcitabine-and-cisplatin-dur8">Durvalumab with gemcitabine and cisplatin (<a href="../CDF_Forms/DUR8.html">DUR8</a>)</h2>
<p>For neoadjuvant treatment then alone adjuvant treatment of muscle-invasive bladder cancer where the following <a href="../CDF_Forms/DUR8.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="durvalumab-with-chemotherapy-dur9" class="level2">
<h2 class="anchored" data-anchor-id="durvalumab-with-chemotherapy-dur9">Durvalumab with chemotherapy (<a href="../CDF_Forms/DUR9.html">DUR9</a>)</h2>
<p>For neoadjuvant and adjuvant treatment then alone for adjuvant treatment of resectable gastric or gastro-oesophageal junction adenocarcinoma where the following <a href="../CDF_Forms/DUR9.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="lisocabtagene-maraleucel-lis02a" class="level2">
<h2 class="anchored" data-anchor-id="lisocabtagene-maraleucel-lis02a">Lisocabtagene maraleucel (<a href="../CDF_Forms/LIS02a.html">LIS02a</a>)</h2>
<p>For treating relapsed/refractory diffuse large B-cell lymphoma (DLBCL), primary mediastinal B-cell lymphoma (PMBCL) and transformed follicular lymphoma (TFL) to DLBCL in patients previously treated with two or more lines of systemic therapy where the following <a href="../CDF_Forms/LIS02a.html">criteria</a> have been met This form is for the approval of leucapheresis and manufacture of CAR-T cells. There is a second part to this form which relates to the subsequent infusion of CAR-T cells and this will be available after submission of the first part. The second part of the form (LIS02b) can only be completed as a continuation of this first part of the form (LIS02a) and must be completed on infusion of CAR-T cells otherwise the treating Trust will not be reimbursed for the cost of lisocabtagene maraleucel.</p>
<p><strong>Date moving into routine commissioning updated</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.402.html</guid>
  <pubDate>Thu, 04 Jun 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
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  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.401.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.401) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Friday 29, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="serplulimab-in-combination-with-carboplatin-and-etoposide-ser1" class="level2">
<h2 class="anchored" data-anchor-id="serplulimab-in-combination-with-carboplatin-and-etoposide-ser1">Serplulimab in combination with carboplatin and etoposide (<a href="../CDF_Forms/SER1.html">SER1</a>)</h2>
<p>For the first-line treatment of adult patients with extensive-stage small cell lung cancer where the following <a href="../CDF_Forms/SER1.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="atezolizumab-in-combination-with-nab--paclitaxel-ate6" class="level2">
<h2 class="anchored" data-anchor-id="atezolizumab-in-combination-with-nab--paclitaxel-ate6">Atezolizumab in combination with nab- paclitaxel (<a href="../CDF_Forms/ATE6.html">ATE6</a>)</h2>
<p>For treating untreated PD-L1-positive, triple negative, unresectable, locally advanced metastatic breast cancer for patients whose tumours express PD-L1 at a level of 1% or more where the following <a href="../CDF_Forms/ATE6.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1 and 12) updated; Treatment criterion (#2 and 13) removed</strong></p>
</section>
<section id="na-bre3" class="level2">
<h2 class="anchored" data-anchor-id="na-bre3">NA (<a href="../CDF_Forms/BRE3.html">BRE3</a>)</h2>
<p>NA</p>
<p><strong>Indication column updated; Treatment criterion (#1, 5 and 7) updated</strong></p>
</section>
<section id="na-bre5" class="level2">
<h2 class="anchored" data-anchor-id="na-bre5">NA (<a href="../CDF_Forms/BRE5.html">BRE5</a>)</h2>
<p>NA</p>
<p><strong>Indication column updated; Treatment criterion (#1, 6 and 9) updated</strong></p>
</section>
<section id="pertuzumab-per2a" class="level2">
<h2 class="anchored" data-anchor-id="pertuzumab-per2a">Pertuzumab (<a href="../CDF_Forms/PER2a.html">PER2a</a>)</h2>
<p>Neoadjuvant pertuzumab plus trastuzumab in NODE POSITIVE patients for the neoadjuvant treatment of locally advanced, inflammatory or early breast cancer at high risk of recurrence (PER2a) where the following criteria have been met This form is for patients known to be pathologically node positive prior to commencing neo-adjuvant therapy. On commencing adjuvant treatment with pertuzumab, form PER4a (for node positive patients) must be completed. For patients with locally advanced, inflammatory or early breast cancer who are node negative of unknown nodal status when commencing neo- adjuvant pertuzumab, form PER2b must be used for the neoadjuvant part of treatment followed by form PER4b for the adjuvant part of treatment only if the histology post-surgery is node +ve.</p>
<p><strong>Treatment criterion (#1 and 8) updated</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.401.html</guid>
  <pubDate>Thu, 28 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.400.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.400) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Tuesday 26, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="cemiplimab-with-platinum-based-chemotherapy-cem2" class="level2">
<h2 class="anchored" data-anchor-id="cemiplimab-with-platinum-based-chemotherapy-cem2">Cemiplimab with platinum-based chemotherapy (<a href="../CDF_Forms/CEM2.html">CEM2</a>)</h2>
<p>For untreated advanced non-small-cell lung cancer where the following <a href="../CDF_Forms/CEM2.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.400.html</guid>
  <pubDate>Mon, 25 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
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<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.399.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.399) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 21, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="tisotumab-vedotin-tisv1" class="level2">
<h2 class="anchored" data-anchor-id="tisotumab-vedotin-tisv1">Tisotumab vedotin (<a href="../CDF_Forms/TISV1.html">TISV1</a>)</h2>
<p>For treating recurrent or metastatic cervical cancer that has progressed on or after systemic treatment where the following <a href="../CDF_Forms/TISV1.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="durvalumab-with-chemotherapy-dur9" class="level2">
<h2 class="anchored" data-anchor-id="durvalumab-with-chemotherapy-dur9">Durvalumab with chemotherapy (<a href="../CDF_Forms/DUR9.html">DUR9</a>)</h2>
<p>For neoadjuvant and adjuvant treatment then alone for adjuvant treatment of resectable gastric or gastro-oesophageal junction adenocarcinoma where the following <a href="../CDF_Forms/DUR9.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#4) updated</strong></p>
</section>
<section id="pembrolizumab-pemb8" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb8">Pembrolizumab (<a href="../CDF_Forms/PEMB8.html">PEMB8</a>)</h2>
<p>Pembrolizumab in combination with pemetrexed- and platinum-based chemotherapy for the first line treatment of PD-L1 positive or negative locally advanced or metastatic non-squamous non-small cell lung cancer where all the following criteria are met:</p>
<p><strong>Treatment criterion (#1 and 6) updated</strong></p>
</section>
<section id="pembrolizumab-in-combination-with-or-nab-paclitaxel-pemb18" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-in-combination-with-or-nab-paclitaxel-pemb18">Pembrolizumab in combination with or nab-paclitaxel (<a href="../CDF_Forms/PEMB18.html">PEMB18</a>)</h2>
<p>The treatment of previously untreated locally advanced unresectable or metastatic triple negative breast cancer patients with PD-L1 expression test results of immune cell (IC) &lt;1% and a combined positive score (CPS) of 10 or more where the following <a href="../CDF_Forms/PEMB18.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 9 and 14) updated; Treatment criterion (#2 and 15) removed</strong></p>
</section>
<section id="pembrolizumab-monotherapy-pemb31" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-monotherapy-pemb31">Pembrolizumab monotherapy (<a href="../CDF_Forms/PEMB31.html">PEMB31</a>)</h2>
<p>Pembrolizumab MONOTHERAPY for adjuvant treatment after complete tumour resection in adult patients with UICC/AJCC 8th edition stage IIA or IIB or IIIA or N2 only IIIB non-small cell lung cancer and whose disease has not progressed on recently completed adjuvant platinum-based chemotherapy where the following <a href="../CDF_Forms/PEMB31.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#1, 12 and 16) updated; Treatment criterion (#2, 17 and 18) removed</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.399.html</guid>
  <pubDate>Wed, 20 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.398.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.398) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Tuesday 19, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="lisocabtagene-maraleucel-lis02a" class="level2">
<h2 class="anchored" data-anchor-id="lisocabtagene-maraleucel-lis02a">Lisocabtagene maraleucel (<a href="../CDF_Forms/LIS02a.html">LIS02a</a>)</h2>
<p>For treating relapsed/refractory diffuse large B-cell lymphoma (DLBCL), primary mediastinal B-cell lymphoma (PMBCL) and transformed follicular lymphoma (TFL) to DLBCL in patients previously treated with two or more lines of systemic therapy where the following <a href="../CDF_Forms/LIS02a.html">criteria</a> have been met This form is for the approval of leucapheresis and manufacture of CAR-T cells. There is a second part to this form which relates to the subsequent infusion of CAR-T cells and this will be available after submission of the first part. The second part of the form (LIS02b) can only be completed as a continuation of this first part of the form (LIS02a) and must be completed on infusion of CAR-T cells otherwise the treating Trust will not be reimbursed for the cost of lisocabtagene maraleucel.</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2" class="level2">
<h2 class="anchored" data-anchor-id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2">Belantamab mafodotin with pomalidomide and dexamethasone (<a href="../CDF_Forms/BELA2.html">BELA2</a>)</h2>
<p>Belantamab mafodotin with pomalidomide and dexamethasone as 2nd line treatment of relapsed or refractory myeloma in adult patients who previously received lenalidomide as part of 1st line systemic therapy where the following <a href="../CDF_Forms/BELA2.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.398.html</guid>
  <pubDate>Tue, 19 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.397.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.397) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 14, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="durvalumab-with-chemotherapy-dur9" class="level2">
<h2 class="anchored" data-anchor-id="durvalumab-with-chemotherapy-dur9">Durvalumab with chemotherapy (<a href="../CDF_Forms/DUR9.html">DUR9</a>)</h2>
<p>For neoadjuvant and adjuvant treatment then alone for adjuvant treatment of resectable gastric or gastro-oesophageal junction adenocarcinoma where the following <a href="../CDF_Forms/DUR9.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="niraparib-nir3" class="level2">
<h2 class="anchored" data-anchor-id="niraparib-nir3">Niraparib (<a href="../CDF_Forms/NIR3.html">NIR3</a>)</h2>
<p>Niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy AND who HAVE deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation [NICE TA673] where the following <a href="../CDF_Forms/NIR3.html">criteria</a> have been met There is a separate form NIR4 for use of niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy and who DO NOT HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="talazoparib-plus-enzalutamide-tal2" class="level2">
<h2 class="anchored" data-anchor-id="talazoparib-plus-enzalutamide-tal2">Talazoparib plus enzalutamide (<a href="../CDF_Forms/TAL2.html">TAL2</a>)</h2>
<p>For the treatment of metastatic hormone- relapsed (castrate-resistant) prostate cancer in patients who are treatment naïve to androgen receptor inhibitors and in whom chemotherapy is not yet clinically indicated or appropriate where the following <a href="../CDF_Forms/TAL2.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="cetuximab-in-combination-with-fluoropyrimidine-based-chemotherapy-cet5" class="level2">
<h2 class="anchored" data-anchor-id="cetuximab-in-combination-with-fluoropyrimidine-based-chemotherapy-cet5">Cetuximab in combination with fluoropyrimidine-based chemotherapy (<a href="../CDF_Forms/CET5.html">CET5</a>)</h2>
<p>For chemotherapy-naive metastatic or locally advanced and inoperable colorectal cancer where all the following criteria are met:</p>
<p><strong>Added to section B, merging forms CET1, CET2 and CET4</strong></p>
</section>
<section id="panitumumab-in-combination-with-fluoropyrimidine-based-chemotherapy-pan4" class="level2">
<h2 class="anchored" data-anchor-id="panitumumab-in-combination-with-fluoropyrimidine-based-chemotherapy-pan4">Panitumumab in combination with fluoropyrimidine-based chemotherapy (<a href="../CDF_Forms/PAN4.html">PAN4</a>)</h2>
<p>For chemotherapy-naive metastatic or locally advanced and inoperable colorectal cancer where the following criteria are met: Panobinostat for treating multiple</p>
<p><strong>Added to section B, merging forms PAN1, PAN2 and PAN3</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.397.html</guid>
  <pubDate>Thu, 14 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
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  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.395.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.395) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 7, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="osimertinib-monotherapy-osi5" class="level2">
<h2 class="anchored" data-anchor-id="osimertinib-monotherapy-osi5">Osimertinib monotherapy (<a href="../CDF_Forms/OSI5.html">OSI5</a>)</h2>
<p>For treating EGFR mutation positive unresectable locally advanced non-small- cell lung cancer after platinum-based chemoradiotherapy where the following <a href="../CDF_Forms/OSI5.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="pembrolizumab-pemb35" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb35">Pembrolizumab (<a href="../CDF_Forms/PEMB35.html">PEMB35</a>)</h2>
<p>Neo-adjuvant followed by adjuvant pembrolizumab for stage III macroscopic resectable melanoma in people 12 years and over where the following <a href="../CDF_Forms/PEMB35.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning (NHS England clinical commissioning policy), added to section B</strong></p>
</section>
<section id="belantamab-mafodotin-in-combination-with-bortezomib-and-dexamethasone-bela1" class="level2">
<h2 class="anchored" data-anchor-id="belantamab-mafodotin-in-combination-with-bortezomib-and-dexamethasone-bela1">Belantamab mafodotin in combination with bortezomib and dexamethasone (<a href="../CDF_Forms/BELA1.html">BELA1</a>)</h2>
<p>Belantamab mafodotin in combination with bortezomib and dexamethasone as 2nd line treatment of relapsed or refractory myeloma in adult patients where the following <a href="../CDF_Forms/BELA1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated; Treatment criterion (#1 and 4) updated; Treatment criterion (#11, 12, 13, 14 and 15) removed</strong></p>
</section>
<section id="encorafenib-in-combination-with-binimetinib-enc3" class="level2">
<h2 class="anchored" data-anchor-id="encorafenib-in-combination-with-binimetinib-enc3">Encorafenib in combination with binimetinib (<a href="../CDF_Forms/ENC3.html">ENC3</a>)</h2>
<p>For the first line treatment of metastatic BRAF V600 mutation positive non-small cell lung cancer where the following <a href="../CDF_Forms/ENC3.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="ripretinib-rip1" class="level2">
<h2 class="anchored" data-anchor-id="ripretinib-rip1">Ripretinib (<a href="../CDF_Forms/RIP1.html">RIP1</a>)</h2>
<p>Ripretinib for treating advanced gastrointestinal stromal tumours after 3 or more kinase inhibitors where the following <a href="../CDF_Forms/RIP1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="vorasidenib-vor1" class="level2">
<h2 class="anchored" data-anchor-id="vorasidenib-vor1">Vorasidenib (<a href="../CDF_Forms/VOR1.html">VOR1</a>)</h2>
<p>For treating astrocytoma or oligodendroglioma with IDH1 or IDH2 mutations after surgery in patients aged 12 years and over where the following <a href="../CDF_Forms/VOR1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="zanidatamab-zani1" class="level2">
<h2 class="anchored" data-anchor-id="zanidatamab-zani1">Zanidatamab (<a href="../CDF_Forms/ZANI1.html">ZANI1</a>)</h2>
<p>For the treatment of HER2-positive advanced biliary tract cancer after 1 or more lines of systemic treatment where the following <a href="../CDF_Forms/ZANI1.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated; Treatment criterion (#2, 3 and 5) updated</strong></p>
</section>
<section id="na-bos1" class="level2">
<h2 class="anchored" data-anchor-id="na-bos1">NA (<a href="../CDF_Forms/BOS1.html">BOS1</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-caba1" class="level2">
<h2 class="anchored" data-anchor-id="na-caba1">NA (<a href="../CDF_Forms/CABA1.html">CABA1</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-das6" class="level2">
<h2 class="anchored" data-anchor-id="na-das6">NA (<a href="../CDF_Forms/DAS6.html">DAS6</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-erib1" class="level2">
<h2 class="anchored" data-anchor-id="na-erib1">NA (<a href="../CDF_Forms/ERIB1.html">ERIB1</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-eve1" class="level2">
<h2 class="anchored" data-anchor-id="na-eve1">NA (<a href="../CDF_Forms/EVE1.html">EVE1</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-eve5" class="level2">
<h2 class="anchored" data-anchor-id="na-eve5">NA (<a href="../CDF_Forms/EVE5.html">EVE5</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-eve6" class="level2">
<h2 class="anchored" data-anchor-id="na-eve6">NA (<a href="../CDF_Forms/EVE6.html">EVE6</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-eve7" class="level2">
<h2 class="anchored" data-anchor-id="na-eve7">NA (<a href="../CDF_Forms/EVE7.html">EVE7</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-sor2" class="level2">
<h2 class="anchored" data-anchor-id="na-sor2">NA (<a href="../CDF_Forms/SOR2.html">SOR2</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-sor3" class="level2">
<h2 class="anchored" data-anchor-id="na-sor3">NA (<a href="../CDF_Forms/SOR3.html">SOR3</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="na-sor5" class="level2">
<h2 class="anchored" data-anchor-id="na-sor5">NA (<a href="../CDF_Forms/SOR5.html">SOR5</a>)</h2>
<p>NA</p>
<p><strong>Removed from section B</strong></p>
</section>
<section id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2" class="level2">
<h2 class="anchored" data-anchor-id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2">Belantamab mafodotin with pomalidomide and dexamethasone (<a href="../CDF_Forms/BELA2.html">BELA2</a>)</h2>
<p>Belantamab mafodotin with pomalidomide and dexamethasone as 2nd line treatment of relapsed or refractory myeloma in adult patients who previously received lenalidomide as part of 1st line systemic therapy where the following <a href="../CDF_Forms/BELA2.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#1) updated; Treatment criterion (#12, 13, 14, 15 and 16) removed</strong></p>
</section>
<section id="nivolumab-niv25" class="level2">
<h2 class="anchored" data-anchor-id="nivolumab-niv25">Nivolumab (<a href="../CDF_Forms/NIV25.html">NIV25</a>)</h2>
<p>Nivolumab plus chemotherapy for neoadjuvant treatment and then continued as adjuvant monotherapy in adults with previously untreated UICC/AJCC 8th edition stage IIA or IIB or IIIA or N2 only IIIB non- small cell lung cancer AND who are candidates for potentially curative surgery where the following <a href="../CDF_Forms/NIV25.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#6) updated</strong></p>
</section>
<section id="pembrolizumab-pemb17" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb17">Pembrolizumab (<a href="../CDF_Forms/PEMB17.html">PEMB17</a>)</h2>
<p>Pembrolizumab monotherapy for relapsed/refractory classical Hodgkin lymphoma in patients aged 3 years and older who have NOT been previously treated with stem cell transplantation brentuximab vedotin</p>
<p><strong>Treatment criterion (#1, 11, 13 and 14) updated; Treatment criterion (#2 and 14) removed</strong></p>
</section>
<section id="pembrolizumab-pemb34" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb34">Pembrolizumab (<a href="../CDF_Forms/PEMB34.html">PEMB34</a>)</h2>
<p>Pembrolizumab for resectable, locally advanced, head and neck squamous cell carcinoma in adults whose tumours express PD-L1 with a combined positive score of 1 or more where the following <a href="../CDF_Forms/PEMB34.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#7 and 8) updated</strong></p>
</section>
<section id="na-tec1" class="level2">
<h2 class="anchored" data-anchor-id="na-tec1">NA (<a href="../CDF_Forms/TEC1.html">TEC1</a>)</h2>
<p>NA</p>
<p><strong>‘Drug’ column updated; Treatment criterion (#1, 9 and 15) updated; Treatment criterion (#14, 15, 16, 17, 18, 19, 20, 21 and 23) removed</strong></p>
</section>
<section id="amivantamab-in-combination-with-lazertinib-ami1" class="level2">
<h2 class="anchored" data-anchor-id="amivantamab-in-combination-with-lazertinib-ami1">Amivantamab in combination with lazertinib (<a href="../CDF_Forms/AMI1.html">AMI1</a>)</h2>
<p>For the first line treatment of locally advanced or metastatic non-small cell lung cancer in adults whose tumours have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations where the following <a href="../CDF_Forms/AMI1.html">criteria</a> have been met</p>
<p><strong>Correction of ‘Date baseline funding started’</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.395.html</guid>
  <pubDate>Thu, 07 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.396.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.396) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Friday 8, May 2026.</p>
<p>The following changes have been introduced:</p>
<section id="amivantamab-with-carboplatin-and-pemetrexed-ami2" class="level2">
<h2 class="anchored" data-anchor-id="amivantamab-with-carboplatin-and-pemetrexed-ami2">Amivantamab with carboplatin and pemetrexed (<a href="../CDF_Forms/AMI2.html">AMI2</a>)</h2>
<p>Amivantamab with carboplatin and pemetrexed for untreated EGFR exon 20 insertion mutation-positive advanced, non- squamous, non-small-cell lung cancer where the following <a href="../CDF_Forms/AMI2.html">criteria</a> have been met</p>
<p><strong>Recommended for the CDF</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.396.html</guid>
  <pubDate>Thu, 07 May 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.394.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.394) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Tuesday 21, April 2026.</p>
<p>The following changes have been introduced:</p>
<section id="encorafenib-in-combination-with-binimetinib-enc3" class="level2">
<h2 class="anchored" data-anchor-id="encorafenib-in-combination-with-binimetinib-enc3">Encorafenib in combination with binimetinib (<a href="../CDF_Forms/ENC3.html">ENC3</a>)</h2>
<p>For the first line treatment of metastatic BRAF V600 mutation positive non-small cell lung cancer where the following <a href="../CDF_Forms/ENC3.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="zanidatamab-zani1" class="level2">
<h2 class="anchored" data-anchor-id="zanidatamab-zani1">Zanidatamab (<a href="../CDF_Forms/ZANI1.html">ZANI1</a>)</h2>
<p>For the treatment of HER2-positive advanced biliary tract cancer after 1 or more lines of systemic treatment where the following <a href="../CDF_Forms/ZANI1.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="amivantamab-in-combination-with-lazertinib-ami1" class="level2">
<h2 class="anchored" data-anchor-id="amivantamab-in-combination-with-lazertinib-ami1">Amivantamab in combination with lazertinib (<a href="../CDF_Forms/AMI1.html">AMI1</a>)</h2>
<p>For the first line treatment of locally advanced or metastatic non-small cell lung cancer in adults whose tumours have epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations where the following <a href="../CDF_Forms/AMI1.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="blinatumomab-bli3" class="level2">
<h2 class="anchored" data-anchor-id="blinatumomab-bli3">Blinatumomab (<a href="../CDF_Forms/BLI3.html">BLI3</a>)</h2>
<p>The treatment of patients in first complete haematological complete remission and with minimal residual disease post 1st line induction chemotherapy in B-precursor acute lymphoblastic leukaemia in ADULT patients where all the following criteria are met:</p>
<p><strong>Treatment criterion (#11) updated</strong></p>
</section>
<section id="blinatumomab-bli4" class="level2">
<h2 class="anchored" data-anchor-id="blinatumomab-bli4">Blinatumomab (<a href="../CDF_Forms/BLI4.html">BLI4</a>)</h2>
<p>The treatment of patients in first complete haematological remission and with minimal residual disease post 1st line induction chemotherapy in B-precursor acute lymphoblastic leukaemia in CHILD patients where all the following criteria have been met:</p>
<p><strong>Treatment criterion (#12) updated</strong></p>
</section>
<section id="blinatumomab-bli5" class="level2">
<h2 class="anchored" data-anchor-id="blinatumomab-bli5">Blinatumomab (<a href="../CDF_Forms/BLI5.html">BLI5</a>)</h2>
<p>The treatment of ADULT patients in first morphological complete remission and without minimal residual disease after line intensive induction and intensification chemotherapy for Philadelphia chromosome negative B-cell precursor acute lymphoblastic leukaemiawhere all the following criteria are met:</p>
<p><strong>Treatment criteria (#4 and 10) updated</strong></p>
</section>
<section id="blinatumomab-bli6" class="level2">
<h2 class="anchored" data-anchor-id="blinatumomab-bli6">Blinatumomab (<a href="../CDF_Forms/BLI6.html">BLI6</a>)</h2>
<p>The treatment of POST PUBESCENT CHILDREN in first morphological complete remission and without minimal residual disease after 1st line intensive induction and any indicated intensification chemotherapy for Philadelphia chromosome negative B-cell precursor acute lymphoblastic leukaemia where the following <a href="../CDF_Forms/BLI6.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#4) updated</strong></p>
</section>
<section id="dabrafenib-in-combination-with-trametinib-dabtra3" class="level2">
<h2 class="anchored" data-anchor-id="dabrafenib-in-combination-with-trametinib-dabtra3">Dabrafenib in combination with trametinib (<a href="../CDF_Forms/DABTRA3.html">DABTRA3</a>)</h2>
<p>For the first line treatment of metastatic BRAF V600 mutation positive non-small cell lung cancer where the following <a href="../CDF_Forms/DABTRA3.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#1, 5 and 10 updated)</strong></p>
</section>
<section id="pembrolizumab-pemb5" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb5">Pembrolizumab (<a href="../CDF_Forms/PEMB5.html">PEMB5</a>)</h2>
<p>The treatment of relapsed or refractory classical Hodgkin lymphoma in ADULTS who are stem cell transplant-ineligible and have failed brentuximab vedotin where the following <a href="../CDF_Forms/PEMB5.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#8, 9 and 12) updated</strong></p>
</section>
<section id="pembrolizumab-monotherapy-pemb25" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-monotherapy-pemb25">Pembrolizumab monotherapy (<a href="../CDF_Forms/PEMB25.html">PEMB25</a>)</h2>
<p>For the treatment of patients with ENDOMETRIAL carcinoma exhibiting microsatellite instability (MSI-H) or deficient mismatch repair (dMMR) and who have progressive disease during or following prior platinum-containing therapy given in any setting for advanced or recurrent or metastatic disease and who are not candidates for potentially curative surgery or radiotherapy or chemoradiotherapy where the following <a href="../CDF_Forms/PEMB25.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#1, 8, 10 and 12) updated</strong></p>
</section>
<section id="venetoclax-in-combination-with-azacitidine-ven8" class="level2">
<h2 class="anchored" data-anchor-id="venetoclax-in-combination-with-azacitidine-ven8">Venetoclax in combination with azacitidine (<a href="../CDF_Forms/VEN8.html">VEN8</a>)</h2>
<p>For untreated adult acute myeloid leukaemia in patients unsuitable for intensive chemotherapy where the following <a href="../CDF_Forms/VEN8.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#5 and 11) updated</strong></p>
</section>
<section id="pembrolizumab-pemb34" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb34">Pembrolizumab (<a href="../CDF_Forms/PEMB34.html">PEMB34</a>)</h2>
<p>Pembrolizumab for resectable, locally advanced, head and neck squamous cell carcinoma in adults whose tumours express PD-L1 with a combined positive score of 1 or more where the following <a href="../CDF_Forms/PEMB34.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.394.html</guid>
  <pubDate>Mon, 20 Apr 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.392.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.392) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Wednesday 1, April 2026.</p>
<p>The following changes have been introduced:</p>
<section id="ripretinib-rip1" class="level2">
<h2 class="anchored" data-anchor-id="ripretinib-rip1">Ripretinib (<a href="../CDF_Forms/RIP1.html">RIP1</a>)</h2>
<p>Ripretinib for treating advanced gastrointestinal stromal tumours after 3 or more kinase inhibitors where the following <a href="../CDF_Forms/RIP1.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="vorasidenib-vor1" class="level2">
<h2 class="anchored" data-anchor-id="vorasidenib-vor1">Vorasidenib (<a href="../CDF_Forms/VOR1.html">VOR1</a>)</h2>
<p>For treating astrocytoma or oligodendroglioma with IDH1 or IDH2 mutations after surgery in patients aged 12 years and over where the following <a href="../CDF_Forms/VOR1.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2" class="level2">
<h2 class="anchored" data-anchor-id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2">Belantamab mafodotin with pomalidomide and dexamethasone (<a href="../CDF_Forms/BELA2.html">BELA2</a>)</h2>
<p>Belantamab mafodotin with pomalidomide and dexamethasone as 2nd line treatment of relapsed or refractory myeloma in adult patients who previously received lenalidomide as part of 1st line systemic therapy where the following <a href="../CDF_Forms/BELA2.html">criteria</a> have been met</p>
<p><strong>Correction - Moved into section A of list; Date moving into routine commissioning updated</strong></p>
</section>
<section id="niraparib-nir3-niraparib-nir3" class="level2">
<h2 class="anchored" data-anchor-id="niraparib-nir3-niraparib-nir3">Niraparib (<a href="../CDF_Forms/NIR3.html">NIR3</a>) ## Niraparib (<a href="../CDF_Forms/NIR3.html">NIR3</a>)</h2>
<p>Niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy AND who HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation [NICE TA673] where the following <a href="../CDF_Forms/NIR3.html">criteria</a> have been met There is a separate form NIR4 for use of niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy and who DO NOT HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation Niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy AND who HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation (TA673) where the following <a href="../CDF_Forms/NIR3.html">criteria</a> have been met There is a separate form NIR4 for use of niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy and who DO NOT HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation</p>
<p><strong>Correction - Moved into section A of list; Date moving into routine commissioning updated Correction - Moved into section A of list; Date moving into routine commissioning updated</strong></p>
</section>
<section id="niraparib-nir3-niraparib-nir3-1" class="level2">
<h2 class="anchored" data-anchor-id="niraparib-nir3-niraparib-nir3-1">Niraparib (<a href="../CDF_Forms/NIR3.html">NIR3</a>) ## Niraparib (<a href="../CDF_Forms/NIR3.html">NIR3</a>)</h2>
<p>Niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy AND who HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation [NICE TA673] where the following <a href="../CDF_Forms/NIR3.html">criteria</a> have been met There is a separate form NIR4 for use of niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy and who DO NOT HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation Niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy AND who HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation (TA673) where the following <a href="../CDF_Forms/NIR3.html">criteria</a> have been met There is a separate form NIR4 for use of niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy and who DO NOT HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation</p>
<p><strong>Correction - Moved into section A of list; Date moving into routine commissioning updated Correction - Moved into section A of list; Date moving into routine commissioning updated</strong></p>
</section>
<section id="talazoparib-plus-enzalutamide-tal2" class="level2">
<h2 class="anchored" data-anchor-id="talazoparib-plus-enzalutamide-tal2">Talazoparib plus enzalutamide (<a href="../CDF_Forms/TAL2.html">TAL2</a>)</h2>
<p>For the treatment of metastatic hormone- relapsed (castrate-resistant) prostate cancer in patients who are treatment naïve to androgen receptor inhibitors and in whom chemotherapy is not yet clinically indicated or appropriate where the following <a href="../CDF_Forms/TAL2.html">criteria</a> have been met</p>
<p><strong>Correction - Moved into section A of list; Date moving into routine commissioning updated</strong></p>
</section>
<section id="na-ven7" class="level2">
<h2 class="anchored" data-anchor-id="na-ven7">NA (<a href="../CDF_Forms/VEN7.html">VEN7</a>)</h2>
<p>NA</p>
<p><strong>Removed from section A</strong></p>
</section>
<section id="venetoclax-in-combination-with-obinutuzumab-ven6" class="level2">
<h2 class="anchored" data-anchor-id="venetoclax-in-combination-with-obinutuzumab-ven6">Venetoclax in combination with obinutuzumab (<a href="../CDF_Forms/VEN6.html">VEN6</a>)</h2>
<p>For the treatment of patients with previously untreated chronic lymphatic leukaemia which doesn’t have a 17p deletion or TP53 mutation where the following <a href="../CDF_Forms/VEN6.html">criteria</a> have been met</p>
<p><strong>Indication column updated; Several treatment criterion updated; combined with previous VEN7 form</strong></p>
</section>
<section id="epcoritamab-monotherapy-epc2" class="level2">
<h2 class="anchored" data-anchor-id="epcoritamab-monotherapy-epc2">Epcoritamab monotherapy (<a href="../CDF_Forms/EPC2.html">EPC2</a>)</h2>
<p>Epcoritamab monotherapy for previously treated adult patients with relapsed/refractory follicular lymphoma who have received 2 or more lines of systemic therapy where the following <a href="../CDF_Forms/EPC2.html">criteria</a> have been met</p>
<p><strong>Correction of Date moving into routine commissioning</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.392.html</guid>
  <pubDate>Wed, 01 Apr 2026 23:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.391.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.391) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Thursday 26, March 2026.</p>
<p>The following changes have been introduced:</p>
<section id="pembrolizumab-pemb34" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb34">Pembrolizumab (<a href="../CDF_Forms/PEMB34.html">PEMB34</a>)</h2>
<p>Pembrolizumab for resectable, locally advanced, head and neck squamous cell carcinoma in adults whose tumours express PD-L1 with a combined positive score of 1 or more where the following <a href="../CDF_Forms/PEMB34.html">criteria</a> have been met</p>
<p><strong>Correction of ‘Available to new patients’</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.391.html</guid>
  <pubDate>Thu, 26 Mar 2026 00:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.390.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.390) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Tuesday 24, March 2026.</p>
<p>The following changes have been introduced:</p>
<section id="pembrolizumab-pemb34" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb34">Pembrolizumab (<a href="../CDF_Forms/PEMB34.html">PEMB34</a>)</h2>
<p>Pembrolizumab for resectable, locally advanced, head and neck squamous cell carcinoma in adults whose tumours express PD-L1 with a combined positive score of 1 or more where the following <a href="../CDF_Forms/PEMB34.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2" class="level2">
<h2 class="anchored" data-anchor-id="belantamab-mafodotin-with-pomalidomide-and-dexamethasone-bela2">Belantamab mafodotin with pomalidomide and dexamethasone (<a href="../CDF_Forms/BELA2.html">BELA2</a>)</h2>
<p>Belantamab mafodotin with pomalidomide and dexamethasone as 2nd line treatment of relapsed or refractory myeloma in adult patients who previously received lenalidomide as part of 1st line systemic therapy where the following <a href="../CDF_Forms/BELA2.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="na-dos3" class="level2">
<h2 class="anchored" data-anchor-id="na-dos3">NA (<a href="../CDF_Forms/DOS3.html">DOS3</a>)</h2>
<p>NA</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="niraparib-nir3" class="level2">
<h2 class="anchored" data-anchor-id="niraparib-nir3">Niraparib (<a href="../CDF_Forms/NIR3.html">NIR3</a>)</h2>
<p>Niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy AND who HAVE deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation [NICE TA673] where the following <a href="../CDF_Forms/NIR3.html">criteria</a> have been met There is a separate form NIR4 for use of niraparib monotherapy as maintenance treatment in patients with high grade epithelial stage III or IV ovarian, fallopian tube or primary peritoneal carcinoma who are in response following platinum-based FIRST line chemotherapy and who DO NOT HAVE a deleterious or suspected deleterious BRCA germline and/or somatic BRCA mutation</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="obecabtagene-autoleucel-obe01a" class="level2">
<h2 class="anchored" data-anchor-id="obecabtagene-autoleucel-obe01a">Obecabtagene autoleucel (<a href="../CDF_Forms/OBE01a.html">OBE01a</a>)</h2>
<p>Obecabtagene autoleucel (obecel) CAR-T cells for treating relapsed/refractory Philadelphia negative or positive B cell precursor acute lymphoblastic leukaemia in patients aged 26 years and older where the following <a href="../CDF_Forms/OBE01a.html">criteria</a> have been met This form is for the approval of leucapheresis and manufacture of CAR-T cells. There is a second part to this form which relates to the subsequent infusion of CAR-T cells and this will be available after submission of the first part. The second part of the form (OBE01b) can only be completed as a continuation of this first part of the form (OBE01a) and OBE01b must be completed on infusion CAR-T cells otherwise the treating Trust will not be reimbursed for the cost of obecabtagene autoleucel (obecel). Note: the second part of the form (OBE01b) will only appear after the above first part of the form (OBE01a) has been fully completed and submitted. To complete the second part of the form, the user will have to complete a continuation request for the OBE1a application.</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="talazoparib-plus-enzalutamide-tal2" class="level2">
<h2 class="anchored" data-anchor-id="talazoparib-plus-enzalutamide-tal2">Talazoparib plus enzalutamide (<a href="../CDF_Forms/TAL2.html">TAL2</a>)</h2>
<p>For the treatment of metastatic hormone- relapsed (castrate-resistant) prostate cancer in patients who are treatment naïve to androgen receptor inhibitors and in whom chemotherapy is not yet clinically indicated or appropriate where the following <a href="../CDF_Forms/TAL2.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="epcoritamab-monotherapy-epc2" class="level2">
<h2 class="anchored" data-anchor-id="epcoritamab-monotherapy-epc2">Epcoritamab monotherapy (<a href="../CDF_Forms/EPC2.html">EPC2</a>)</h2>
<p>Epcoritamab monotherapy for previously treated adult patients with relapsed/refractory follicular lymphoma who have received 2 or more lines of systemic therapy where the following <a href="../CDF_Forms/EPC2.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="lenvatinib-with-everolimus-lnv1" class="level2">
<h2 class="anchored" data-anchor-id="lenvatinib-with-everolimus-lnv1">Lenvatinib with everolimus (<a href="../CDF_Forms/LNV1.html">LNV1</a>)</h2>
<p>The treatment of previously treated advanced renal cell carcinoma</p>
<p><strong>Treatment criterion (#10 and 11) updated; Treatment criteria (#10) removed</strong></p>
</section>
<section id="trastuzumab-emtansine-monotherapy-tra2" class="level2">
<h2 class="anchored" data-anchor-id="trastuzumab-emtansine-monotherapy-tra2">Trastuzumab emtansine MONOTHERAPY (<a href="../CDF_Forms/TRA2.html">TRA2</a>)</h2>
<p>As adjuvant therapy for patients with HER2-positive early breast cancer who have residual invasive disease following the combination of taxane-based and HER2-targeted neoadjuvant systemic therapy and surgery where the following <a href="../CDF_Forms/TRA2.html">criteria</a> have been met</p>
<p><strong>Drug column updated; Treatment criterion (#5 and 10) updated; Treatment criterion (#7 and 11) removed</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.390.html</guid>
  <pubDate>Wed, 25 Mar 2026 00:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.389.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.389) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Sunday 22, March 2026.</p>
<p>The following changes have been introduced:</p>
<section id="nivolumab-niv25" class="level2">
<h2 class="anchored" data-anchor-id="nivolumab-niv25">Nivolumab (<a href="../CDF_Forms/NIV25.html">NIV25</a>)</h2>
<p>Nivolumab plus chemotherapy for neoadjuvant treatment and then continued as adjuvant monotherapy in adults with previously untreated UICC/AJCC 8th edition stage IIA or IIB or IIIA or N2 only IIIB non- small cell lung cancer AND who are candidates for potentially curative surgery where the following <a href="../CDF_Forms/NIV25.html">criteria</a> have been met</p>
<p><strong>Correction of Nice Approved Indication</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.389.html</guid>
  <pubDate>Fri, 20 Mar 2026 00:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.388.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.388) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Monday 9, March 2026.</p>
<p>The following changes have been introduced:</p>
<section id="glofitamab-in-combinaton-with-gemcitabine-and-oxaliplatin-glo2" class="level2">
<h2 class="anchored" data-anchor-id="glofitamab-in-combinaton-with-gemcitabine-and-oxaliplatin-glo2">Glofitamab in combinaton with gemcitabine and oxaliplatin (<a href="../CDF_Forms/GLO2.html">GLO2</a>)</h2>
<p>Glofitamab with gemcitabine and oxaliplatin for treating relapsed or refractory diffuse large B- cell lymphoma where the following <a href="../CDF_Forms/GLO2.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="talquetamab-monotherapy-talq1" class="level2">
<h2 class="anchored" data-anchor-id="talquetamab-monotherapy-talq1">Talquetamab monotherapy (<a href="../CDF_Forms/TALQ1.html">TALQ1</a>)</h2>
<p>For treating relapsed or refractory multiple myeloma after 3 or more treatments where the following <a href="../CDF_Forms/TALQ1.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list</strong></p>
</section>
<section id="nivolumab-niv25-nivolumab-niv25" class="level2">
<h2 class="anchored" data-anchor-id="nivolumab-niv25-nivolumab-niv25">Nivolumab (<a href="../CDF_Forms/NIV25.html">NIV25</a>) ## Nivolumab (<a href="../CDF_Forms/NIV25.html">NIV25</a>)</h2>
<p>Nivolumab plus ipilimumab for previously untreated patients with microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) metastatic or locally advanced and inoperable colorectal cancer where the following <a href="../CDF_Forms/NIV25.html">criteria</a> have been met Nivolumab plus ipilimumab for previously untreated patients with microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) metastatic or locally advanced and inoperable colorectal cancer where the following <a href="../CDF_Forms/NIV25.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list; Treatment criteria (#9) updated Treatment criteria (#9) updated</strong></p>
</section>
<section id="durvalumab-with-gemcitabine-and-cisplatin-dur8" class="level2">
<h2 class="anchored" data-anchor-id="durvalumab-with-gemcitabine-and-cisplatin-dur8">Durvalumab with gemcitabine and cisplatin (<a href="../CDF_Forms/DUR8.html">DUR8</a>)</h2>
<p>For neoadjuvant treatment then alone for adjuvant treatment of muscle-invasive bladder cancer where the following <a href="../CDF_Forms/DUR8.html">criteria</a> have been met</p>
<p><strong>Date moving into routine commissioning updated</strong></p>
</section>
<section id="bevacizumab-with-first-line-fluoropyrimidine-based-chemotherapy-bev11" class="level2">
<h2 class="anchored" data-anchor-id="bevacizumab-with-first-line-fluoropyrimidine-based-chemotherapy-bev11">Bevacizumab with FIRST LINE fluoropyrimidine-based chemotherapy (<a href="../CDF_Forms/BEV11.html">BEV11</a>)</h2>
<p>For metastatic or locally advanced and inoperable colorectal cancer where the following <a href="../CDF_Forms/BEV11.html">criteria</a> have been met</p>
<p><strong>‘TA’ and ‘Date of Final NICE Guidance’ columns updated</strong></p>
</section>
<section id="nivolumab-niv25-nivolumab-niv25-1" class="level2">
<h2 class="anchored" data-anchor-id="nivolumab-niv25-nivolumab-niv25-1">Nivolumab (<a href="../CDF_Forms/NIV25.html">NIV25</a>) ## Nivolumab (<a href="../CDF_Forms/NIV25.html">NIV25</a>)</h2>
<p>Nivolumab plus ipilimumab for previously untreated patients with microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) metastatic or locally advanced and inoperable colorectal cancer where the following <a href="../CDF_Forms/NIV25.html">criteria</a> have been met Nivolumab plus ipilimumab for previously untreated patients with microsatellite instability high (MSI-H) or mismatch repair deficient (dMMR) metastatic or locally advanced and inoperable colorectal cancer where the following <a href="../CDF_Forms/NIV25.html">criteria</a> have been met</p>
<p><strong>Moved into routine commissioning - section B of list; Treatment criteria (#9) updated Treatment criteria (#9) updated</strong></p>
</section>
<section id="pembrolizumab-pemb9a" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb9a">Pembrolizumab (<a href="../CDF_Forms/PEMB9a.html">PEMB9a</a>)</h2>
<p>Pembrolizumab monotherapy for treating unresectable or advanced malignant melanoma (form a): REGISTRATION OF START OF PEMBROLIZUMAB MONOTHERAPY OR OF PREVIOUSLY COMMENCED AND CURRENTLY CONTINUED PEMBROLIZUMAB MONOTHERAPY This form comes in 3 parts. 1. The first part is for patients who are either scheduled to commence pembrolizumab monotherapy or who commenced and continue to receive pembrolizumab monotherapy. 2. The second part of the form which must use the same unique Blueteq identifier is for those benefitting patients who choose to electively discontinue pembrolizumab after 2 or more years of treatment; this second part (patient details be automatically entered) will only appear once the first part of the form is approved and should be completed at the time of elective discontinuation of pembrolizumab. 3. The third part of the form which must use the same unique Blueteq identifier is for those patients registered as having electively and previously stopped pembrolizumab and in whom there is disease progression for which the clinician wishes to re-commence pembrolizumab; this third part of the form (patient details will automatically entered) will only appear once second part of the form has been approved.</p>
<p><strong>Treatment criteria (#9) updated</strong></p>
</section>
<section id="pembrolizumab-in-combination-with-platinum-and-fluoropyrimidine-based-chemotherapy-pemb15" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-in-combination-with-platinum-and-fluoropyrimidine-based-chemotherapy-pemb15">Pembrolizumab in combination with platinum and fluoropyrimidine-based chemotherapy (<a href="../CDF_Forms/PEMB15.html">PEMB15</a>)</h2>
<p>For previously untreated advanced oesophageal carcinoma which expresses PD-L1 with a combined positive score of 10 or more where the following <a href="../CDF_Forms/PEMB15.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#9, 10 and 12) updated; Treatment criterion (#2 and 13) removed</strong></p>
</section>
<section id="pembrolizumab-in-combination-with-lenvatinib-pemb23" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-in-combination-with-lenvatinib-pemb23">Pembrolizumab in combination with lenvatinib (<a href="../CDF_Forms/PEMB23.html">PEMB23</a>)</h2>
<p>For the treatment of patients with endometrial carcinoma who have progressive disease during or following prior platinum-containing therapy given any setting for advanced or recurrent or metastatic disease and who are not candidates for potentially curative surgery or radiotherapy or chemoradiotherapy where the following <a href="../CDF_Forms/PEMB23.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#8, 9, 10, 11, 13 and 15) updated; Treatment criterion (#2, 10 and 17) removed</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.388.html</guid>
  <pubDate>Tue, 10 Mar 2026 00:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
<item>
  <title>NHS England updates CDF List</title>
  <link>https://updates.chemo.org.uk/news/CDFNews_1.387.html</link>
  <description><![CDATA[ 




<section id="nhs-england-updates-cdf-list" class="level1">
<h1>NHS England updates CDF List</h1>
<p>NHS England has updated the Cancer Drugs Fund List. The latest version (v1.387) was uploaded to the <a href="https://www.england.nhs.uk/publication/national-cancer-drugs-fund-list/">NHS England Website</a> on Monday 23, February 2026.</p>
<p>The following changes have been introduced:</p>
<section id="epcoritamab-monotherapy-epc2" class="level2">
<h2 class="anchored" data-anchor-id="epcoritamab-monotherapy-epc2">Epcoritamab monotherapy (<a href="../CDF_Forms/EPC2.html">EPC2</a>)</h2>
<p>Epcoritamab monotherapy for previously treated adult patients with relapsed/refractory follicular lymphoma who have received 2 or more lines of systemic therapy where the following <a href="../CDF_Forms/EPC2.html">criteria</a> have been met</p>
<p><strong>Recommended for routine commissioning, receiving CDF interim funding</strong></p>
</section>
<section id="carfilzomib-in-combination-with-lenalidomide-and-dexamethasone-car2" class="level2">
<h2 class="anchored" data-anchor-id="carfilzomib-in-combination-with-lenalidomide-and-dexamethasone-car2">Carfilzomib in combination with lenalidomide and dexamethasone (<a href="../CDF_Forms/CAR2.html">CAR2</a>)</h2>
<p>For the treatment of previously treated multiple myeloma in patients who have had 1 prior line of systemic therapy where the following <a href="../CDF_Forms/CAR2.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#6 and 13) updated; Treatment criteria (#13) removed</strong></p>
</section>
<section id="pembrolizumab-pemb7" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb7">Pembrolizumab (<a href="../CDF_Forms/PEMB7.html">PEMB7</a>)</h2>
<p>Pembrolizumab for adjuvant treatment melanoma with high risk of recurrence where the following <a href="../CDF_Forms/PEMB7.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#10) updated; Treatment criterion (#2 and 11) removed</strong></p>
</section>
<section id="pembrolizumab-pemb8" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb8">Pembrolizumab (<a href="../CDF_Forms/PEMB8.html">PEMB8</a>)</h2>
<p>Pembrolizumab in combination with pemetrexed- and platinum-based chemotherapy for the first line treatment of PD-L1 positive or negative locally advanced or metastatic non-squamous non-small cell lung cancer where all the following criteria are met:</p>
<p><strong>Treatment criteria (#13) updated; Treatment criterion (#2 and 14) removed</strong></p>
</section>
<section id="pembrolizumab-pemb12" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb12">Pembrolizumab (<a href="../CDF_Forms/PEMB12.html">PEMB12</a>)</h2>
<p>For previously untreated metastatic or unresectable recurrent PD-L1 positive head and neck squamous cell carcinoma (HNSCC) where the following <a href="../CDF_Forms/PEMB12.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#6, 7 and 10) updated; Treatment criteria (#2) removed</strong></p>
</section>
<section id="pembrolizumab-pemb14" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb14">Pembrolizumab (<a href="../CDF_Forms/PEMB14.html">PEMB14</a>)</h2>
<p>For the 1st line treatment of patients with either metastatic or locally advanced and inoperable colorectal cancer exhibiting microsatellite instability-high (MSI-H) or mismatch repair deficiency (dMMR) where the following <a href="../CDF_Forms/PEMB14.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#10 and 12) updated; Treatment criterion (#2, 13 and 15) removed</strong></p>
</section>
<section id="pembrolizumab-pemb19" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb19">Pembrolizumab (<a href="../CDF_Forms/PEMB19.html">PEMB19</a>)</h2>
<p>Pembrolizumab monotherapy for adjuvant treatment after complete tumour resection of renal cell carcinoma in adult patients at increased risk of recurrence following nephrectomy or following nephrectomy and resection of all metastatic disease where the following <a href="../CDF_Forms/PEMB19.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#8, 10 and 11) updated; Treatment criterion (#2, 11 and 13) removed</strong></p>
</section>
<section id="pembrolizumab-pemb20" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb20">Pembrolizumab (<a href="../CDF_Forms/PEMB20.html">PEMB20</a>)</h2>
<p>Pembrolizumab for the adjuvant treatment of newly diagnosed and completely resected stage IIB or stage IIC malignant melanoma where the following <a href="../CDF_Forms/PEMB20.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#10) updated; Treatment criterion (#2 and 11) removed</strong></p>
</section>
<section id="pembrolizumab-pemb21" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-pemb21">Pembrolizumab (<a href="../CDF_Forms/PEMB21.html">PEMB21</a>)</h2>
<p>Pembrolizumab in combination with chemotherapy as neoadjuvant treatment and then continued as adjuvant monotherapy after definitive surgery for patients with previously untreated locally advanced or early stage triple negative breast cancer at high risk of recurrence where the following <a href="../CDF_Forms/PEMB21.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#10, 13, 15 and 17) updated; Treatment criterion (#2 and 18) removed</strong></p>
</section>
<section id="pembrolizumab-in-combination-with-chemotherapy-with-or-without-bevacizumab-pemb22" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-in-combination-with-chemotherapy-with-or-without-bevacizumab-pemb22">Pembrolizumab in combination with chemotherapy with or without bevacizumab (<a href="../CDF_Forms/PEMB22.html">PEMB22</a>)</h2>
<p>For the treatment of persistent, recurrent or metastatic cervical cancer in patients whose tumour PD-L1 expression test results have a combined positive score (CPS) of 1 or more where the following <a href="../CDF_Forms/PEMB22.html">criteria</a> have been met</p>
<p><strong>Treatment criterion (#10, 11, 15 and 16) updated; Treatment criterion (#2 and 16) removed</strong></p>
</section>
<section id="pembrolizumab-in-combination-with-chemotherapy-pemb30" class="level2">
<h2 class="anchored" data-anchor-id="pembrolizumab-in-combination-with-chemotherapy-pemb30">Pembrolizumab in combination with chemotherapy (<a href="../CDF_Forms/PEMB30.html">PEMB30</a>)</h2>
<p>Pembrolizumab in combination with chemotherapy for neoadjuvant treatment and then continued as adjuvant monotherapy in adults with previously untreated UICC/AJCC 8th edition stage IIA or IIB or IIIA or N2 only IIIB non-small cell lung cancer AND who are candidates for potentially curative surgery where the following <a href="../CDF_Forms/PEMB30.html">criteria</a> have been met</p>
<p><strong>Treatment criteria (#9) updated</strong></p>


</section>
</section>

 ]]></description>
  <category>News</category>
  <category>CDF</category>
  <guid>https://updates.chemo.org.uk/news/CDFNews_1.387.html</guid>
  <pubDate>Tue, 24 Feb 2026 00:00:00 GMT</pubDate>
  <media:content url="https://updates.chemo.org.uk/images/BlueteqForm.jpeg" medium="image" type="image/jpeg"/>
</item>
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