| Literature DB >> 32984932 |
Clinton Yam1, Gaiane M Rauch2, Tanbin Rahman3, Meghan Karuturi1, Elizabeth Ravenberg1, Jason White1, Alyson Clayborn1, Pamela McCarthy1, Sausan Abouharb1, Bora Lim1, Jennifer K Litton1, David L Ramirez1, Sadia Saleem1, James Stec4, W Fraser Symmans5, Lei Huo6, Senthil Damodaran1, Ryan Sun3, Stacy L Moulder7.
Abstract
Folate receptor alpha (FRα) has been reported to be expressed in up to 80% of triple-negative breast cancers (TNBC) with limited expression in normal tissues, making it a promising therapeutic target. Mirvetuximab soravtansine (mirvetuximab-s) is an antibody drug conjugate which has shown promise in the treatment of FRα-positive solid tumors in early phase clinical trials. Herein, are the results of the first prospective phase II trial evaluating mirvetuximab-s in metastatic TNBC. Patients with advanced, FRα-positive TNBC were enrolled on this study. Mirvetuximab-s was administered at a dose of 6.0 mg/kg every 3 weeks. 96 patients with advanced TNBC consented for screening. FRα staining was performed on tumor tissue obtained from 80 patients. The rate of FRα positivity by immunohistochemistry was 10.0% (8/80). Two patients were treated on study, with best overall responses of stable disease in one and progressive disease in the other. Adverse events were consistent with earlier studies. The study was terminated early due to the low rate of FRα positivity in the screened patient population and lack of disease response in the two patients treated. The observed rate of FRα positivity was considerably lower than previously reported and none of the patients had a partial or complete response. Treatment with mirvetuximab-s should only be further explored in TNBC if an alternate biomarker strategy is developed for patient selection on the basis of additional preclinical data.Entities:
Keywords: Antibody-drug conjugate; Mirvetuximab soravtansine; Phase II trial; Triple-negative breast Cancer
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Year: 2020 PMID: 32984932 DOI: 10.1007/s10637-020-00995-2
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850