Archived: azacitidine (Vidaza)
Advice
Following a full submission
azacitidine (Vidaza ®) is not recommended for use within NHS Scotland.
Licensed indication under review: the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (SCT) with intermediate-2 and high-risk myelodysplastic syndrome (MDS), chronic myelomonocytic leukaemia (CMML) or acute myeloid leukaemia (AML).
Azacitidine therapy produced a significant increase in overall survival compared with conventional care regimens in previously untreated higher-risk MDS patients.
However, the manufacturer did not present a sufficiently robust economic analysis and their justification for the treatment’s cost in relation to its health benefits was not sufficient to gain acceptance by SMC.
Drug Details
| Drug Name: | azacitidine (Vidaza) |
|---|---|
| SMC Drug ID: | 589/09 |
| Manufacturer: | Celgene Ltd |
| Indication: | Treatment of adult patients not eligible for haematopoietic stem cell transplantation with: myelodysplastic syndrome / chronic myelomonocytic leukaemia / acute myeloid leukaemia |
| BNF Category: | |
| Sub Category: | 8.1 Cytotoxic drugs |
| Submission Type: | Full submission |
| Status: | Not Recommended |
| Date Advice Published: | 12 April 2010 |
Current Advice
| azacitidine (Vidaza) | Resubmission | 12 September 2011 |