A phase 2 study of vatalanib in metastatic melanoma patients☆
Abstract
Background
A phase 2 study of vatalanib (PTK787/ZK222584) an oral tyrosine kinase inhibitor of VEGFR 1, 2 and 3 was undertaken in patients with metastatic melanoma.
Methods
Adults with pathologically confirmed metastatic melanoma, WHO Performance status 0–2, and adequate haematological, hepatic and renal function, were treated with vatalanib until disease progression. The trial used Fleming’s single stage design.
Results
Tumour control rate (CR
+
PR
+
SD) was 35% at 16
weeks, with objective response seen in only 1 patient. Median progression-free survival was 1.8
months (95% CI 1.8–3.7
months) and median overall survival was 6.5
months (95% CI 3.9–10.2
months).
Conclusion
Vatalanib stabilised disease in a proportion of patients, although overall survival was disappointing.
Keywords: NGR-hTNF, Vascular targeting agent, Colorectal cancer
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☆ Research Support: This study was sponsored by Cambridge University Hospitals NHS Foundation Trust, adopted by the UK National Cancer Research Institute (NCRI), supported by grants from Bayer Schering Pharma and Addenbrooke’s Charitable Trust. M.R.M. is supported by the NIHR Biomedical Research Centre, Oxford.
PII: S0959-8049(10)00692-1
doi:10.1016/j.ejca.2010.07.014
© 2010 Elsevier Ltd. All rights reserved.
