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Naumann RW , Coleman RL , Burger RA , Sausville EA , Kutarska E , Ghamande SA , Gabrail NY , DePasquale SE , Nowara E , Gilbert L , Gersh RH , Teneriello MG , Harb WA , Konstantinopoulos PA , Penson RT , Symanowski JT , Lovejoy CD , Leaman CP , Morgenstern DE , Messmann RA
PRECEDENT: A Randomized Phase II Trial Comparing Vintafolide (EC145) and Pegylated Liposomal Doxorubicin (PLD) in Combination Versus PLD Alone in Patients With Platinum-Resistant Ovarian Cancer
Journal of Clinical Oncology. 2013 Dec;31(35) :4400-+
PMID: WOS:000328817400005   
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Purpose Vintafolide (EC145) is a folic acid-desacetylvinblastine conjugate that binds to the folate receptor (FR), which is expressed on the majority of epithelial ovarian cancers. This randomized phase II trial evaluated vintafolide combined with pegylated liposomal doxorubicin (PLD) compared with PLD alone. The utility of an FR-targeted imaging agent, Tc-99m-etarfolatide (EC20), in selecting patients likely to benefit from vintafolide was also examined. Patients and Methods Women with recurrent platinum-resistant ovarian cancer who had undergone two prior cytotoxic regimens were randomly assigned at a 2:1 ratio to PLD (50 mg/m(2) intravenously [IV] once every 28 days) with or without vintafolide (2.5 mg IV three times per week during weeks 1 and 3). Etarfolatide scanning was optional. The primary objective was to compare progression-free survival (PFS) between the groups. Results The intent-to-treat population comprised 149 patients. Median PFS was 5.0 and 2.7 months for the vintafolide plus PLD and PLD-alone arms, respectively (hazard ratio [HR], 0.63; 95% CI, 0.41 to 0.96; P = .031). The greatest benefit was observed in patients with 100% of lesions positive for FR, with median PFS of 5.5 compared with 1.5 months for PLD alone (HR, 0.38; 95% CI, 0.17 to 0.85; P = .013). The group of patients with FR-positive disease (10% to 90%) experienced some PFS improvement (HR, 0.873), whereas patients with disease that did not express FR experienced no PFS benefit (HR, 1.806). Conclusion Vintafolide plus PLD is the first combination to demonstrate an improvement over standard therapy in a randomized trial of patients with platinum-resistant ovarian cancer. Etarfolatide can identify patients likely to benefit from vintafolide.
Naumann, R. Wendel Coleman, Robert L. Burger, Robert A. Sausville, Edward A. Kutarska, Elzbieta Ghamande, Sharad A. Gabrail, Nashat Y. DePasquale, Stephen E. Nowara, Elzbieta Gilbert, Lucy Gersh, Robert H. Teneriello, Michael G. Harb, Wael A. Konstantinopoulos, Panagiotis A. Penson, Richard T. Symanowski, James T. Lovejoy, Chandra D. Leaman, Christopher P. Morgenstern, David E. Messmann, Richard A.