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SMC says yes to nilotinib for first line use

 

Newly diagnosed Scottish patients will be offered Tasigna (nilotinib) see below:

Sandy 

Advice

Following a full submission:

nilotinib 150mg hard capsules (Tasigna®) is accepted for use within NHS Scotland.

Indication under review: for the treatment of adult patients with newly diagnosed Philadelphia chromosome positive chronic myelogenous leukaemia (CML) in the chronic phase.

First-line treatment with nilotinib in newly diagnosed patients has resulted in significantly higher molecular and cytogenetic response rates compared to the standard tyrosine kinase inhibitor. Further longer term follow-up data are needed to confirm the duration of this response and assess the impact on disease progression and overall survival.

This SMC advice takes account of the benefits of a Patient Access Scheme (PAS) that improves the cost-effectiveness of nilotinib. This SMC advice is contingent upon the continuing availability of the PAS in NHS Scotland

 

 

Drug Details

Drug Name:

nilotinib (Tasigna)

SMC Drug ID:

709/11

Manufacturer:

Novartis Pharmaceuticals UK Ltd

Indication:

For the treatment of adult patients with newly diagnosed Philadelphia chromosome positive chronic myelogenous leukaemia (CML) in the chronic phase.

BNF Category:

8. Malignant disease and immunosuppression

Sub Category:

8.1 Cytotoxic drugs

Submission Type:

Full submission

Status:

Accepted

Date Advice Published:

8 August 2011

http://www.scottishmedicines.org.uk/SMC_Advice/Advice/709_11_nilotinib_Tasigna/nilotinib_Tasigna

Interesting to see the guidance is contingent on and takes account of the patient access scheme offered by Novartis.

hi Rchard... yes and I am assuming we might see something similar from NICE re nilotinib, although the appraisal was for second line use rather than in the SMC case for first line- the PAS offer from Novartis (but not BMS) certainly has had an effect. 

Sandy