Following a full submission
AWMSG advice |
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Status: Recommended with restrictions | |||
Lapatinib (Tyverb®) is recommended as an option for restricted use within NHS Wales for the treatment of adult patients with breast cancer, whose tumours overexpress HER2 (ErbB2), in combination with capecitabine for patients with advanced or metastatic disease with progression following prior therapy, which must have included anthracyclines and taxanes and therapy with trastuzumab in the metastatic setting. Lapatinib (Tyverb®) should be restricted within its licensed indication for the treatment of patients as an alternative to treatment with trastuzumab and capecitabine or trastuzumab and vinorelbine in patients in whom clinicians consider this clinically appropriate. Lapatinib (Tyverb®) is not recommended for use within NHS Wales outside of this subpopulation. This recommendation applies only in circumstances where the approved Wales Patient Access Scheme is utilised. |
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Medicine details |
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Medicine name | lapatinib (Tyverb®) | ||
Formulation | 250 mg film-coated tablet | ||
Reference number | 178 | ||
Indication | Treatment of adult patients with breast cancer, whose tumours overexpress HER2 (ErbB2), in combination with capecitabine for patients with advanced or metastatic disease with progression following prior therapy, which must have included anthracyclines and taxanes and therapy with trastuzumab in the metastatic setting |
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Company | Novartis Pharmaceuticals UK Ltd | ||
BNF chapter | Malignant disease & immunosuppression | ||
Submission type | Full | ||
Status | Recommended with restrictions | ||
Advice number | 1713 | ||
NMG meeting date | 19/06/2013 | ||
AWMSG meeting date | 17/07/2013 | ||
Ratification by Welsh Government | 14/08/2013 | ||
Date of issue | 15/08/2013 | ||
Date of last review | 30/09/2016 | ||
Commercial arrangement | WPAS |