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Myelodysplastic syndromes - azacitidine

Azacitidine for the treatment of myelodyplastic syndrome, chronic myelomonocytic leukaemia, and acute myeloid leukaemia

Status: History
Expected date of issue: TBC
Referral date: July 2008
Wave: 18
Process: STA
Topic area:
  • Cancer
 

NICE project team

Executive Lead: Peter Littlejohns
Technical Lead: Scott Goulden
Communications manager: Alice Law
Project manager: Jeremy Powell
Evidence review group: West Midlands Health Technology Assessment Collaboration
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Provisional schedule

Closing date for invited submissions / evidence submission: TBC
1st appraisal committee meeting: 01 July 2009
2nd appraisal committee meeting 03 September 2010
3rd appraisal committee meeting: 07 January 2010
4th appraisal committee meeting: 06 October 2010
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Consultees and commentators

Consultees Commentators (no right to submit or appeal)

Manufacturers/sponsors

  • Celgene (azacitidine)

Patient/carer groups

  • Leukaemia CARE
  • Leukaemia Research Fund
  • Leukaemia Society (UK)
  • Macmillan Cancer Support
  • MDS Patient Support Group
  • Rarer Cancers Forum

Professional groups

  • British Committee for Standardisation in Haematology
  • British Society for Haematology
  • Cancer Research UK
  • Royal College of Nursing
  • Royal College of Pathologists
  • Royal College of Physicians, Medical Oncology Joint Special Committee
  • United Kingdom Oncology Nursing Society

Others

  • Department of Health
  • Harrow PCT
  • Stockton-On-Tees PCT
  • Welsh Assembly Government

General

  • Department of Health, Social Services and Public Safety for Northern Ireland
  • NHS Quality Improvement Scotland

Comparator manufacturers

  • Cephalon (doxorubicin) (CA&U not returned, not participating)
  • Hospira UK (cytarabine, doxorubicin) (CA&U not returned, not participating)
  • Pharmacia/Pfizer (cytarabine, doxorubicin)
  • Schering Plough (doxorubicin) (CA&U not returned, not participating)
  • Winthrop Pharmaceuticals UK/Sanofi Aventis (daunorubicin)
  • Wockhardt UK (doxorubicin) (CA&U not returned, not participating)
  • Zeneus (doxorubicin) (CA&U not returned, not participating)

Relevant research groups

  • None

Evidence Review Group

  • National Institute for Health Research Health Technology Assessment Programme
  • West Midlands Health Technology Assessment Collaboration

Associated Guideline Groups

  • National Collaborating Centre for Cancer

Associated Public Health Groups

  • None

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Project history

Date Update
8 October 2009 The manufacturer has submitted substantial comments on the ACD and a Patient Access Scheme. The Committee has requested clarification from the manufacturer and this will be critiqued by the ERG and considered by the Committee on 3 November 2009.
22 July 2010 In line with the decision of the Appeal Panel, NICE will be seeking further information from MDS UK and from Celgene . This information will then be reviewed by an academic group before being considered by the Appraisal Committee.
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Key documents

This page was last updated: 22 March 2011

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Selected, reliable information for health and social care in one place

Accessibility | Cymraeg | Freedom of information | Vision Impaired | Contact Us | Glossary | Data protection | Copyright | Disclaimer | Terms and conditions

Copyright @ 2012 National Institute for Health and Clinical Excellence. All rights reserved.