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Updated: Apr 30, 2026

Quantitation of Intra-peritoneal Ovarian Cancer Metastasis
Published on: July 18, 2016
Vintafolide: a novel targeted agent for epithelial ovarian cancer
Whitney S Graybill1, Robert L Coleman
1Medical University of South Carolina, Division of Gynecologic Oncology, 96 Jonathan Lucas Street, CSB 634, MSC 619, Charleston, SC, USA.
Abstract:
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. (99m)Tc-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.
Insights
Vintafolide, a novel folate-drug conjugate, shows promise in treating ovarian cancer by targeting the folate receptor. Combination therapy with pegylated liposomal doxorubicin significantly improved progression-free survival in platinum-resistant cases.
Area of Science:
- Oncology
- Pharmacology
- Radiopharmaceuticals
Background:
- Vintafolide (EC145) is a novel folate-conjugated vinca alkaloid (desacetylvinblastine hydrazide; DAVBLH).
- It exhibits high affinity binding to the folate receptor (FR), which is prevalent in epithelial ovarian cancers.
- Preclinical studies indicated significant antiproliferative activity and good tolerability for vintafolide.
Purpose of the Study:
- To evaluate the efficacy and safety of vintafolide in combination with pegylated liposomal doxorubicin (PLD) for platinum-resistant ovarian cancer.
- To assess the role of (99m)Tc-etarfolatide in identifying patients likely to benefit from vintafolide treatment.
Main Methods:
- Phase II study comparing vintafolide plus PLD versus PLD alone in platinum-resistant ovarian cancer.
- Utilized (99m)Tc-etarfolatide to determine folate receptor (FR) status for patient selection.
- Phase I studies established the safety profile and dose-limiting toxicity (constipation).
Main Results:
- The combination of vintafolide and PLD demonstrated a statistically significant improvement in progression-free survival compared to PLD alone.
- Phase I studies confirmed an acceptable safety profile for vintafolide.
Conclusions:
- Vintafolide in combination with PLD offers a promising therapeutic strategy for patients with platinum-resistant ovarian cancer.
- FR status, determined by (99m)Tc-etarfolatide, can guide treatment selection for vintafolide therapy.
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