Journal
MELANOMA RESEARCH
Volume 22, Issue 4, Pages 294-301Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CMR.0b013e32835312e4
Keywords
cilengitide; melanoma; phase II; alpha(v)beta(3) integrin
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Funding
- National Cancer Institute [N01 CM-17003, N02 CO-12400]
- Cancer Center [CA16672]
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Cilengitide (EMD 121974) is a selective inhibitor of integrins alpha(v)beta(3) and alpha(v)beta(5). The alpha(v)beta(3) promotes the proliferation of tumor-associated endothelial cells and potentially the survival of melanoma cells. We conducted a randomized phase II trial in patients with metastatic melanoma to evaluate the clinical efficacy of cilengitide. Patients with stage IV or unresectable stage III melanoma who were either chemonaive or who had previously received one systemic therapy were enrolled. Patients were randomly assigned to either 500 or 2000 mg of cilengitide administered intravenously twice weekly. The primary aim of this study was to determine the progression-free survival rate at 8 weeks. Tumor samples and blood samples were collected for pharmacodynamic and pharmacokinetic studies. Twenty-nine patients were enrolled, of whom 26 were treated (14 at 500 mg and 12 at 2000 mg). Among those treated, only three were progression free at 8 weeks: two in the 500 mg arm and one in the 2000 mg arm. One patient in the 2000 mg arm showed a prolonged partial response after an initial 28% enlargement of her target lesions. The treatment was well tolerated without clinically significant adverse events. The sole responder and one of two patients with stable disease had no alpha(v)beta(3) expression at baseline. Overall, alpha(v)beta(3) expression was decreased by day 8 of the treatment (P=0.05). Cilengitide was well tolerated by patients in both the treatment arms but had minimal clinical efficacy as a single-agent therapy for metastatic melanoma, and the efficacy was not related to baseline alpha(v)beta(3) expression. Melanoma Res 22:294-301 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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