4.4 Article

Vintafolide: a novel targeted agent for epithelial ovarian cancer

期刊

FUTURE ONCOLOGY
卷 10, 期 4, 页码 541-548

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/FON.14.8

关键词

antigen drug conjugate; EC145; EC20; etarfolatide; folate receptor; ovarian cancer; vinca alkaloid; vintafolide

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资金

  1. Merck

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Vintafolide (EC145) is a novel folate-conjugated vinca alkaloid (desacetylvinblastine hydrazide; DAVBLH) that binds with high affinity to the folate receptor (FR), expressed in a majority of epithelial ovarian cancers. In preclinical studies, vintafolide had significant antiproliferative activity and tolerability. Phase I studies demonstrated an acceptable safety profile, with constipation being the dose-limiting toxicity. A Phase II study of vintafolide plus pegylated liposomal doxorubicin (PLD) versus PLD alone in patients with platinum-resistant ovarian cancer showed a statistically significant improvement in progression-free survival with combination therapy. Tc-99m-etarfolatide, a diagnostic radiopharmaceutical, determines FR status, which allows determination of those patients most likely to benefit from treatment with vintafolide. A Phase III study evaluating vintafolide plus PLD versus PLD alone in patients with platinum-resistant ovarian cancer is currently underway.

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