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Potential Novel Type Of Therapy For Ovarian Cancer

A new antibody-guided drug has shown promising activity in a phase I trial involving with platinum drug-resistant disease, researchers from reported at the annual meeting of the . The findings (abstract LB-290) were discussed at a press conference and later at an oral presentation on Tuesday, April 09, 2013, 4:00 p.m. to 4:20 p.m. in room 146, in the Washington Convention Center.

, MD, MPH, first author of the study, said that among 29 patients who received the at what was found to be the maximum tolerated dose, there was one complete response and four partial responses. “In addition, there were additional patients with prolonged stable disease who were able to stay on treatment,” said Liu, of the gynecologic oncology treatment center at Dana-Farber.

The responses all occurred in patients whose tumors had high expression of the MUC16 protein to which the drug is targeted. Known as DMUC5754A, the drug conjugate consists of an antibody, which recognizes the MUC16 protein expressed by ovarian , fused to a toxin, MMAE, which prevents from dividing. Targeting the drug conjugate specifically to ovarian reduced adverse effects of the toxin on healthy tissues and organs, said Liu. She called the safety profile “encouraging.” Most common adverse effects were fatigue, nausea, and vomiting. This phase 1 multicenter trial is the first use in humans of DMUC5754A, and the responses, which Liu called “a nice sign of activity in a very challenging type of ovarian cancer to treat,” merit further testing in a phase II trial, which is being planned. “If the activity of this drug is confirmed in additional trials, this will represent a novel type of therapy for ovarian cancer,” Liu said.


Senior author of the study is Howard Burris, III, MD, of The Sarah Cannon Research Institute in Nashville.
Research support came from Genentech, developer of the drug.
–Written by Richard Saltus, Dana-Farber Cancer Institute
Dana-Farber Cancer Institute