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Updated: Jul 16, 2025

Surface-enhanced Resonance Raman Scattering Nanoprobe Ratiometry for Detecting Microscopic Ovarian Cancer via Folate Receptor Targeting
Published on: March 25, 2019
Therapeutic strategies targeting folate receptor α for ovarian cancer
Jia Mai1, Limei Wu1,2, Ling Yang1
1Department of Laboratory Medicine, Obstetrics & Gynecology and Pediatrics, West China Second University Hospital, Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Development and Related Diseases of Women and Children Key Laboratory of Sichuan Province, Center of Growth, Metabolism and Aging, State Key Laboratory of Biotherapy and Collaborative Innovation Center of Biotherapy, Sichuan University, Chengdu, Sichuan, China.
Abstract:
Epithelial ovarian cancer (EOC) is the deadliest gynecological cancer, and presents a major clinical challenge due to limited treatment options. Folate receptor alpha (FRα), encoded by the FOLR1 gene, is an attractive therapeutically target due to its prevalent and high expression in EOC cells. Recent basic and translational studies have explored several modalities, such as antibody-drug conjugate (ADC), monoclonal antibodies, small molecules, and folate-drug conjugate, to exploit FRα for EOC treatment. In this review, we summarize the function of FRα, and clinical efficacies of various FRα-based therapeutics. We highlight mirvetuximab soravtansine (MIRV), or Elahere (ImmunoGen), the first FRα-targeting ADC approved by the FDA to treat platinum-resistant ovarian cancer. We discuss potential mechanisms and management of ocular adverse events associated with MIRV administration.
Insights
Epithelial ovarian cancer (EOC) is a deadly gynecological cancer. This review covers Folate Receptor Alpha (FRα)-targeting therapies, including the approved antibody-drug conjugate mirvetuximab soravtansine for EOC treatment.
Area of Science:
- Gynecologic Oncology
- Translational Cancer Research
- Pharmacology
Background:
- Epithelial ovarian cancer (EOC) poses a significant clinical challenge due to limited treatment options.
- Folate receptor alpha (FRα), highly expressed in EOC, is a promising therapeutic target.
- Current research explores various FRα-targeting strategies for EOC treatment.
Purpose of the Study:
- To review the function of FRα and the clinical efficacy of FRα-based therapeutics for EOC.
- To highlight advancements in FRα-targeting agents, including antibody-drug conjugates (ADCs).
- To discuss the first FDA-approved FRα-targeting ADC, mirvetuximab soravtansine, for platinum-resistant ovarian cancer.
Main Methods:
- Literature review of basic and translational studies on FRα and its targeted therapies.
- Analysis of clinical trial data for FRα-based treatments in ovarian cancer.
- Summary of approved FRα-targeting agents and their mechanisms of action.
Main Results:
- FRα is a validated target in EOC, with multiple therapeutic modalities showing promise.
- Mirvetuximab soravtansine (MIRV) is the first FRα-targeting ADC approved for platinum-resistant EOC.
- Various FRα-based therapies, including ADCs, monoclonal antibodies, and conjugates, are under investigation.
Conclusions:
- FRα-targeting therapies represent a significant advancement in EOC treatment, particularly for resistant disease.
- Mirvetuximab soravtansine offers a new therapeutic option for patients with platinum-resistant ovarian cancer.
- Further research into FRα-targeting agents and management of associated adverse events, such as ocular toxicity, is warranted.
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