Changeflow GovPing Healthcare & Life Sciences Pembrolizumab for Neoadjuvant and Adjuvant Trea...
Priority review Guidance Added Final

Pembrolizumab for Neoadjuvant and Adjuvant Treatment of Resectable Head and Neck Cancer

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Summary

NICE has published final technology appraisal guidance TA1145 recommending pembrolizumab (Keytruda) for the neoadjuvant and adjuvant treatment of resectable locally advanced head and neck squamous cell carcinoma in adults. The guidance includes a commercial access agreement with NHS pricing arrangements. NHS commissioners and providers are expected to fund the treatment in accordance with NICE recommendations.

“The application of the recommendations in this guidance is at the discretion of health professionals and their individual patients and do not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of the individual patient, in consultation with the patient and/or their carer or guardian.”

NICE , verbatim from source
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What changed

NICE published final technology appraisal guidance TA1145 recommending pembrolizumab for treating resectable locally advanced head and neck squamous cell carcinoma in adults. The guidance applies to NHS commissioners and providers who must fund treatment when health professionals and patients wish to use it, in accordance with NHS Constitution duties. A commercial access agreement is in place with NHS-specific pricing details available through the Commercial Access and Pricing Portal.

Healthcare professionals should consider this guidance alongside individual patient needs, preferences, and values when making treatment decisions. NHS commissioners should ensure funding is available to implement this recommendation and should assess environmental impact when implementing NICE recommendations.

Archived snapshot

Apr 21, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

Pembrolizumab for neoadjuvant and adjuvant treatment of resectable locally advanced head and neck squamous cell carcinoma

  • Technology appraisal guidance
  • TA1145
  • Published:

21 April 2026

Download guidance (PDF)

Overview

Evidence-based recommendations on pembrolizumab (Keytruda) for treating resectable locally advanced head and neck squamous cell carcinoma in adults.

Last reviewed: 21 April 2026

Next review: This guidance will be reviewed if there is new evidence that is likely to change the recommendations.

Commercial arrangement

There is a commercial access agreement for pembrolizumab. NHS organisations can get details on the Commercial Access and Pricing (CAP) Portal. Non-NHS organisations can contact keiron.hughes@msd.com for details.

Guidance development process

How we develop NICE technology appraisal guidance

Your responsibility

The recommendations in this guidance represent the view of NICE, arrived at after careful consideration of the evidence available. When exercising their judgement, health professionals are expected to take this guidance fully into account, alongside the individual needs, preferences and values of their patients. The application of the recommendations in this guidance is at the discretion of health professionals and their individual patients and do not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of the individual patient, in consultation with the patient and/or their carer or guardian.

All problems (adverse events) related to a medicine or medical device used for treatment or in a procedure should be reported to the Medicines and Healthcare products Regulatory Agency using the Yellow Card Scheme.

Commissioners and/or providers have a responsibility to provide the funding required to enable the guidance to be applied when individual health professionals and their patients wish to use it, in accordance with the NHS Constitution. They should do so in light of their duties to have due regard to the need to eliminate unlawful discrimination, to advance equality of opportunity and to reduce health inequalities.

Commissioners and providers have a responsibility to promote an environmentally sustainable health and care system and should assess and reduce the environmental impact of implementing NICE recommendations wherever possible.

Named provisions

Recommendations Commercial arrangement Guidance development process Your responsibility

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Last updated

Classification

Agency
NICE
Published
April 21st, 2026
Instrument
Guidance
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Substantive
Document ID
TA1145

Who this affects

Applies to
Healthcare providers Pharmaceutical companies Public health authorities
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Pharmaceutical prescribing Health technology assessment Cancer treatment
Geographic scope
United Kingdom GB

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Regulatory Affairs
Topics
Healthcare Medical Devices

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