Related Experiment Video
Updated: Jan 18, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Mirvetuximab Soravtansine: Mechanism of Action, Clinical and Translational Science
Rajeev Menon1, Emarjola Bako2, Shuhan Liu1
1Clinical Pharmacology, AbbVie Inc., North Chicago, Illinois, USA.
Abstract:
Mirvetuximab soravtansine (MIRV) is an antibody-drug conjugate (ADC) composed of the DM4 payload conjugated to a folate receptor α (FRα)-targeting antibody via the cleavable sulfo-SPDB linker. MIRV targets and binds to FRα with high affinity and specificity, releasing the DM4 payload intracellularly following MIRV-FRα complex internalization and degradation. DM4 and its metabolite S-methyl-DM4 suppress microtubule dynamic instability, which triggers cell cycle arrest and apoptosis. Selective FRα-overexpression in ≥ 90% of epithelial ovarian tumor cells and its ability to internalize large molecules make it a highly attractive ADC target for epithelial ovarian cancers (including primary peritoneal and fallopian tube cancers). Although up to 80% of patients initially respond to platinum-based therapies, the majority of tumors will recur and become platinum-resistant. Unfortunately, platinum-resistant ovarian cancer (PROC) carries a poor prognosis with an overall survival of 12-14 months from the time of platinum-resistance, and prior to MIRV approval in 2022, little had changed in treatment options for decades. The MIRV Phase 3 registrational trial (MIRASOL) showed superiority of MIRV vs. chemotherapy (paclitaxel, pegylated liposomal doxorubicin, or topotecan) in patients with high (≥ 75%) FRα-expression PROC, showing an objective response rate of 42% versus 16%, a median progression-free survival of 5.6 versus 4.0 months, and an overall survival of 16.5 versus 12.8 months. Here, we briefly review MIRV mechanism of action, pharmacokinetics, pharmacodynamics, and key clinical efficacy and safety data.
Insights
Mirvetuximab soravtansine (MIRV) is an antibody-drug conjugate effective against platinum-resistant ovarian cancer (PROC) with high folate receptor alpha (FRα) expression. The MIRASOL trial demonstrated MIRV
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Epithelial ovarian cancers (EOCs) frequently overexpress folate receptor alpha (FRα), making it an attractive target for therapy.
- Platinum-resistant ovarian cancer (PROC) has limited treatment options and a poor prognosis, with median survival of 12-14 months.
- Mirvetuximab soravtansine (MIRV) is an antibody-drug conjugate targeting FRα, approved in 2022 for FRα-positive PROC.
Purpose of the Study:
- To review the mechanism of action, pharmacokinetics, pharmacodynamics, and clinical data of mirvetuximab soravtansine (MIRV).
- To highlight the efficacy and safety of MIRV in patients with platinum-resistant ovarian cancer (PROC) and high FRα expression.
Main Methods:
- Review of preclinical and clinical data for mirvetuximab soravtansine (MIRV).
- Analysis of results from the Phase 3 MIRASOL trial comparing MIRV to chemotherapy in FRα-positive PROC.
- Evaluation of objective response rate (ORR), progression-free survival (PFS), and overall survival (OS).
Main Results:
- MIRV demonstrated superior efficacy compared to chemotherapy in high FRα-expressing PROC.
- MIRASOL trial showed MIRV achieved 42% ORR vs. 16% for chemotherapy, with median PFS of 5.6 vs. 4.0 months, and median OS of 16.5 vs. 12.8 months.
- Key clinical efficacy and safety data for MIRV in PROC were reviewed.
Conclusions:
- Mirvetuximab soravtansine (MIRV) offers a significant therapeutic advance for patients with FRα-positive platinum-resistant ovarian cancer (PROC).
- The MIRASOL trial confirmed MIRV's superiority over standard chemotherapy, improving response rates and survival outcomes.
- MIRV represents a crucial new option for a patient population with historically limited treatment choices.
More Related Videos
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Tumor Immunotherapy
Mechanisms of Retrovirus-induced Cancers
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Treatment Resistant Cancers
Microorganisms in Medicine and Therapeutics

