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Pazopanib and the treatment palette for soft-tissue sarcoma

Despite their common mesenchymal origin, soft-tissue sarcomas are heterogeneous and increasing knowledge of their molecular biology will drive future drug development.1 Effective targeting of KIT mutations by imatinib2 for gastrointestinal stromal tumours has been a notable success story in modern s...

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Bibliographic Details
Published in:The Lancet (British edition) 2012-05, Vol.379 (9829), p.1854-1856
Main Author: Bramwell, Vivien HC
Format: Article
Language:English
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Summary:Despite their common mesenchymal origin, soft-tissue sarcomas are heterogeneous and increasing knowledge of their molecular biology will drive future drug development.1 Effective targeting of KIT mutations by imatinib2 for gastrointestinal stromal tumours has been a notable success story in modern sarcoma therapy. Progression-free survival was chosen as the primary endpoint3 because a targeted agent would inhibit growth rather than cause tumour regression, and on the basis of an analysis of a large database of clinical trials by the European Organisation for Research and Treatment of Cancer, suggesting that 3-month progression-free survival of more than 40% for second-line chemotherapy correlates with clinical activity.5 Interpretation of a 3-month increase in progression-free survival in patients with heterogeneous soft-tissue sarcomas depends on accurate documentation of rapid progression before trial entry.
ISSN:0140-6736
1474-547X
DOI:10.1016/S0140-6736(12)60739-9