SORAYA Trial: Antibody-Drug Conjugate Produces Remissions in One-Third of Patients With Drug-Resistant Ovarian Cancer

March 22, 2022 10:22 am

The following article is provided by The Clearity Foundation to support women with ovarian cancer and their families. Learn more about The Clearity Foundation and the services we provide directly to women as they make treatment decisions and navigate emotional impacts of their diagnosis.

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by the ASCO Post Staff

In a clinical trial involving patients with ovarian cancer previously treated with platinum-based chemotherapy, a novel antibody-drug conjugate therapy produced a substantially better response than standard treatments, investigators from Dana-Farber Cancer Institute reported at the Society of Gynecologic Oncology’s (SGO) 2022 Annual Meeting on Women’s Cancer.

The agent, mirvetuximab soravtansine, generated an objective response in nearly 33% of patients participating in the trial. That compares with response rates in the single digits for current treatments in patients whose ovarian cancer doesn’t respond to platinum-based chemotherapy.

The novel agent is one of a growing number of antibody-drug conjugates, which consist of a drug linked to an antibody that directly targets the cancer cell. Mirvetuximab connects an antibody targeting the folate receptor alpha molecule on high-grade serous ovarian cancers to a drug molecule called DM4 that disrupts microtubule formation (microtubules are major components of the cytoskeleton that give shape and structure to cells). The folate receptor protein is far more abundant in some tumor cells than normal cells, making it an attractive target for cancer drugs.

SORAYA Trial

The SORAYA trial enrolled 106 patients with platinum-resistant high-grade serous ovarian cancer that highly expressed folate receptor alpha. All patients were required to have previously received bevacizumab, a drug that blocks tumors from forming blood vessels to take in more oxygen and nutrients. The participants had been treated with up to three prior treatments for their ovarian cancer.

After a median follow-up of 8.1 months, 32.4% of participants had an objective anticancer response, including five who had a complete response. The median duration of response is currently 6.9 months.

Mirvetuximab was well tolerated by study participants. The most common adverse side effects associated with the treatment were blurred vision, keratopathy, and nausea.

Ursula Matulonis, MD
Ursula Matulonis, MD

“These data have the potential to be transformative for [patients with] ovarian cancer and their physicians,” said Ursula Matulonis, MD, Chief of the Division of Gynecologic Oncology at Dana-Farber Cancer Institute and co-principal investigator of the SORAYA study. “In the platinum-resistant setting and particularly in later-line treated patients, response rates with available therapy are in the single digits, with significant toxicities. With an objective response rate above 30%, a duration of response of around 6 months, and a treatment-related discontinuation rate of 7%, mirvetuximab shows impressive activity and tolerability for patients with platinum-resistant ovarian cancer. These data support the future of mirvetuximab as the potential standard of care for patients with folate receptor alpha–positive ovarian cancer.”

This article was published by The ASCO Post.

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