Suggested remit: To appraise the clinical and cost effectiveness of cabozantinib within its marketing authorisation for treating advanced pancreatic or extra-pancreatic neuroendocrine tumours that have progressed after systemic treatment.
 
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 6474

Provisional Schedule

Committee meeting 10 September 2025
Expected publication 19 November 2025

Project Team

Project lead Greg O'Toole

Email enquiries

External Assessment Group BMJ Technology Assessment Group (BMJ-TAG), BMJ

Stakeholders

Companies sponsors Ipsen (cabozantinib)
Others Department of Health and Social Care
  NHS England
Patient carer groups Black Health Agency for Equality
  Bowel Cancer UK
  Cancer Black Care
  Cancer Equality
  Cancer52
  Gist Cancer UK
  Guts UK
  Helen Rollason Cancer Charity
  Independent Cancer Patients Voice
  Insulinoma Support Network
  Macmillan Cancer Support
  Maggie’s Centres
  Marie Curie
  Neuroendocrine Cancer UK
  OG Support
  Pancreatic Cancer Action
  Pancreatic Cancer UK
  South Asian Health Foundation
  Specialised Healthcare Alliance
  Tenovus Cancer Care
Professional groups Association of Cancer Physicians
  British Geriatrics Society
  British Nuclear Medicine Society
  British Oncology Pharmacy Association
  British Psychosocial Oncology Society
  British Society of Gastroenterology
  Cancer Research UK
  Royal College of General Practitioners
  Royal College of Nursing
  Royal College of Pathologists
  Royal College of Physicians
  Royal Pharmaceutical Society
  Royal Society of Medicine
  Society for Endocrinology
  UK Acute Oncology Society
  UK Clinical Pharmacy Association
  UKI NETS
  UK Oncology Nursing Society
Associated public health groups Public Health Wales
  UK Health Security Agency
Comparator companies Accord Healthcare (5-fluorouracil, temozolomide)
  Amarox (capecitabine)
  Baxter (doxorubicin)
  Dr Reddy’s Laboratories (capecitabine, everolimus, sunitinib)
  Esteve Pharmaceuticals (streptozocin)
  Ethypharm UK (everolimus)
  Glenmark Pharmaceuticals (capecitabine)
  Hospira UK (carboplatin, cisplatin, 5-fluorouracil)
  medac GmBH (doxorubicin, 5-fluorouracil,)
  Merck Sharp & Dohme (temozolomide)
  MSN Laboratories (sunitinib)
  Mylan (sunitinib)
  Neon Healthcare (etoposide
  Novartis (everolimus, lutetium (177Lu) oxodotreotide)
  Pfizer (doxorubicin, sunitinib)
  Piramal Critical Care (sunitinib)
  Sandoz (cisplatin, everolimus, sunitinib)
  Seacross (doxorubicin)
  Sun Pharma (temozolomide)
  Teva Pharma (sunitinib)
  Zentiva (sunitinib)
General commentators All Wales Therapeutics and Toxicology Centre
  Allied Health Professionals Federation
  Board of Community Health Councils in Wales
  British National Formulary
  Care Quality Commission
  Department of Health, Social Services and Public Safety for Northern Ireland
  Healthcare Improvement Scotland
  Medicines and Healthcare products Regulatory Agency
  National Association of Primary Care
  National Pharmacy Association
  NHS Confederation
  Scottish Medicines Consortium
  Scottish Society of Gastroenterology
  Welsh Government
  Welsh Health Specialised Services Committee
Relevant research groups Cochrane Gut
  Cochrane Metabolic & Endocrine Disorders Group
  Genomics England
  MRC Clinical Trials Unit
  National Institute for Health Research

Timeline

Key events during the development of the guidance:

Date Update
11 February 2025 Invitation to participate
14 November 2024 - 12 December 2024 Consultation on suggested remit, draft scope and provisional stakeholder list of consultees and commentators: 6474
12 December 2024 Referral
14 November 2024 In progress. Scoping commencing
20 August 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