Ratification Date: 29/07/2025
Next Review Date: 29/07/2027
Fludarabine (Fludara®) – B-cell Chronic Lymphocytic Leukaemia – 2nd line treatment – as per NICE TA 29
| Drug Name (Brand) | Fludarabine (Fludara®) | |||
| Indication | B-cell Chronic Lymphocytic Leukaemia – 2nd line treatment – as per NICE TA 29 | |||
| Traffic Light Classification | Red | |||
| NICE TA (plus link) | Overview | Guidance on the use of fludarabine for B-cell chronic lymphocytic leukaemia | Guidance | NICE | |||
| Further Information:
NICE recommendations, summary of meeting discussions, links to additional supporting docs etc.
NICE September 2001: Oral fludarabine is recommended as second line therapy for B-cell chronic lymphocytic leukaemia (CLL) for patients who have either failed, or are intolerant of, first line chemotherapy, and who would otherwise have received combination chemotherapy of either: a) cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP); b) cyclophosphamide, doxorubicin and prednisolone (CAP) or c) cyclophosphamide, vincristine and prednisolone (CVP).
March 2008: The TAG recommended that all oral anticancer medicines identified by the National Patient Safety Agency (NPSA) in the Rapid Response Report “Risks of incorrect dosing of oral anti-cancer medicines” (January 2008), for which there are no locally agreed shared care protocols, are classified as Red (Hospital Only).
NHS England Specialised Commissioning responsibility from April 2013. |
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| Date of TAG recommendation / ratification | 7/1/2003 | Review Date | ||