Mirvetuximab Soravtansine in Platinum-Resistant Ovarian Cancer.

Clin Med Insights Oncol

Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.

Published: July 2023

AI Article Synopsis

  • - Ovarian cancer is a major health issue, being the second leading cause of death from gynecologic cancers, and managing platinum-resistant cases is particularly difficult with poor outcomes from standard chemotherapy.
  • - Significant research has focused on understanding why treatments fail and finding new strategies, including the development of antibody drug conjugates (ADCs), which target specific tumor antigens while delivering chemotherapy.
  • - Mirvetuximab soravtansine is a specific ADC targeting the folate receptor alpha in ovarian cancer, showing promising results in clinical trials for patients with platinum-resistant disease, and the review discusses its effectiveness, side effects, and potential future applications.

Article Abstract

Ovarian cancer is the second leading cause of death from gynecologic malignancies worldwide. Management of platinum-resistant disease is challenging and clinical outcomes with standard chemotherapy are poor. Over the past decades, significant efforts have been made to understand drug resistance and develop strategies to overcome treatment failure. Antibody drug conjugates (ADCs) are a rapidly growing class of oncologic therapeutics, which combine the ability to target tumor-specific antigens with the cytotoxic effects of chemotherapy. Mirvetuximab soravtansine is an ADC comprising an IgG1 monoclonal antibody against the folate receptor alpha (FRα) conjugated to the cytotoxic maytansinoid effector molecule DM4 that has shown promising clinical activity in patients with FR-α-positive ovarian cancer. This review summarizes current evidence of mirvetuximab soravtansine in platinum-resistant ovarian cancer, focusing on clinical activity, toxicity, and future directions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387675PMC
http://dx.doi.org/10.1177/11795549231187264DOI Listing

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