Ursula A. Matulonis, MD, on Key Findings With Mirvetuximab Soravtansine in FRα-High Ovarian Cancer

Video

Ursula A. Matulonis, MD, discusses key data with mirvetuximab soravtansine for patients with folate receptor α–high platinum-resistant ovarian cancer that read out of the phase 3 SORAYA trial.

Ursula A. Matulonis, MD, Brock-Wilson Family Chair and chief of the Division of Gynecologic Oncology at Dana-Farber Cancer Institute as well as professor of medicine at Harvard Medical School, spoke with CancerNetwork® during The Society of Gynecologic Oncology (SGO) 2022 Annual Meeting on Women’s Cancer about key findings from the phase 3 SORAYA trial (NCT04296890)exploring efficacy of mirvetuximab soravtansine (IMGN853) in patients with folate receptor α (FRα)–high platinum-resistant ovarian cancer.

In addition to describing the therapy’s mechanism of action, Matulonis highlighted the promising response rates it yielded. She also discussed a subgroup analysis in which responses were examined among patients who had previously received a PARP inhibitor.

Transcript:

Mirvetuximab soravtansine is an antibody-drug conjugate that has the antibody to FRα. There’s a cleavable linker. It’s linked to maytansinoid DM4, which is a potent anti-tubulin agent. Patients had platinum-resistant, ovarian cancer—all [had] high-grade serous [disease and had] received prior bevacizumab [Avastin] and up to 3 lines of treatment.

We were aiming to have a 24% response rate vs a 12% response rate because that’s what is seen with single-agent chemotherapy in platinum-resistant ovarian cancer. But what we saw was a 32.4% confirmed overall response rate with 5 complete responses and 29 partial responses. [We are] really pleased with the overall response rate. Additionally, we saw a duration of response of 6.9 months, which was great. Both the overall response rate of 32.4% and the duration of response of 6.9 months held up in 2 predefined subgroups, [including] those [with] 2 prior lines of treatment vs 3 prior lines of treatment. The second subgroup analysis was around prior PARP or no prior PARP inhibitor, so it didn’t matter if patients were more heavily pretreated or if they had received a prior PARP inhibition. They had response rates that were, again, not affected by being more heavily pretreated or having received a prior PARP inhibitor.

Reference

Matulonis UA, Lorusso D, Oaknin A, et al. Efficacy and safety of mirvetuximab soravtansine in patients with platinum-resistant ovarian cancer with high folate receptor alpha expression results from the SORAYA study. Presented at: 2022 SGO Annual Meeting on Womens’ Cancers; March 18-21, 2022; Phoenix, AZ. Abstract 242.

Recent Videos
Patients with mediastinal lymph node involved-lung cancer may benefit from chemoimmunotherapy in the neoadjuvant setting.
Stressing the importance of prompt AE disclosure before they become severe can ensure that a patient can still undergo resection with curative intent.
Thomas Marron, MD, PhD, presented a session on clinical data that established standards of care for stage II and III lung cancer treatment at CFS 2025.
Sonia Jain, PhD, stated that depatuxizumab mafodotin, ABBV-221, and ABBV-321 were 3 of the most prominent ADCs in EGFR-amplified glioblastoma.
Skin toxicities are common with targeted therapies for GI malignancies but can be remedied by preventative measures and a collaboration with dermatology.
Computational models help researchers anticipate how ADCs may behave in later lines of development, while they are still in the early stages.
ADC payloads with high levels of potency can sometimes lead to higher levels of toxicity, which can eliminate the therapeutic window for patients with cancer.
According to Greg Thurber, PhD, target-mediated uptake is the biggest driver of efficacy for antibody-drug conjugates as a cancer treatment.
Antibody-drug conjugates are effective, but strategies such as better understanding the mechanisms of action may lead to enhanced care for patients with cancer. Antibody-drug conjugates are effective, but strategies such as better understanding the mechanisms of action may lead to enhanced care for patients with cancer.
Related Content