Suggested remit: To appraise the clinical and cost effectiveness of pembrolizumab before surgery (neoadjuvant) then with radiotherapy (with or without cisplatin) after surgery (adjuvant) for untreated, resectable, locally advanced, squamous cell head and neck cancer.

Status:
In progress
Technology type:
Medicine
Decision:
Selected
Reason for decision:
Anticipate the topic will be of importance to patients, carers, professionals, commissioners and the health of the public to ensure clinical benefit is realised, inequalities in use addressed, and help them make the best use of NHS resources
Process:
STA Standard
ID number:
6477

Provisional Schedule

Committee meeting:
04 March 2026
Expected publication:
01 July 2026

Project Team

Project lead
Kate Moore

Email enquiries

If you have any queries please email TACommD@nice.org.uk


External Assessment Group:
School of Health and Related Research (ScHARR), University of Sheffield

Stakeholders

Companies sponsors
Merck Sharp & Dohme (pembrolizumab)
Others
Department of Health and Social Care
 
NHS England
Patient carer groups
Swallows Head & Neck Cancer Support Group
 
Head and Neck Cancer UK
Professional groups
Association of Cancer Physicians
 
British Association of Otorhinolaryngologists
 
Cancer Research UK
 
Royal College of Physicians
 
Royal College of Radiologists
Associated public health groups
None
Comparator companies
Merck (cetuximab) (confidentiality agreement signed, participating)
 
Amarox (cisplatin) (confidentiality agreement not signed, not participating)
 
Hospira UK (cisplatin) (confidentiality agreement not signed, not participating)
 
Sandoz (cisplatin) (confidentiality agreement not signed, not participating)
General commentators
All Wales Therapeutics and Toxicology Centre
 
British National Formulary
 
Department of Health, Social Services and Public Safety for Northern Ireland
 
Healthcare Improvement Scotland
 
Medicines and Healthcare products Regulatory Agency
 
NHS Wales Joint Commissioning Committee
 
Scottish Medicines Consortium
 
Welsh Government
Relevant research groups
Institute of Cancer Research

Timeline

Key events during the development of the guidance:

Date Update
29 August 2025 Invitation to participate
24 July 2025 - 07 August 2025 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators
24 July 2025 In progress. Scoping commenced.
12 December 2024 Referral
19 August 2024 Topic selection
16 July 2024 Awaiting development. Status change linked to Topic Selection Decision being set to Selected

For further information on our processes and methods, please see our CHTE processes and methods manual