Dr. Monk on the FDA Approval of Pembrolizumab in Cervical Cancer
Bradley J. Monk, MD, FACOG, FACS, professor, director of the Division of Gynecologic Oncology at Creighton University School of Medicine at St. Joseph’s Hospital and Medical Center in Phoenix, Arizona, discusses the FDA approval of pembrolizumab (Keytruda) for the treatment of advanced cervical cancer with disease progression on or after chemotherapy.
Bradley J. Monk, MD, FACOG, FACS, professor, director of the Division of Gynecologic Oncology at Creighton University School of Medicine at St. Joseph’s Hospital and Medical Center in Phoenix, Arizona, discusses the FDA approval of pembrolizumab (Keytruda) for the treatment of advanced cervical cancer with disease progression on or after chemotherapy.
The approval is based on findings from the phase II KEYNOTE-158 trial, which investigated pembrolizumab in patients with a range of advanced solid tumors who progressed on standard therapy.
Results showed that, at a median follow-up of 11.7 months (range, 0.6-22.7), the overall response rate was 14.3% (95% CI, 7.4-24.1) in 77 PD-L1—positive patients previously treated with more than 1 line of chemotherapy in the metastatic setting. This also included a complete response rate of 2.6% and a partial response rate of 11.7%. Moreover, the median duration of response was not reached, and 91% of responders had a response duration of 6 months or longer.
