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Bevacizumab (Avastin) has failed to demonstrate statistically significant improvements in overall survival (OS) for women with recurrent ovarian cancer in 2 recent clinical trials, but those results may be affected by factors not related to the drug’s efficacy, according to Michael J. Birrer, MD, PhD.
“The drug works. We’ve had very dramatic responses, particularly for women with ascites, and that’s based upon the mechanism of action,” Birrer said in a recent interview. “The only real controversy is, how should we give it so that women get the maximum benefit. Should they get it up front? Should they get it in maintenance? Or should they get it in recurrence?”
Both phase III trials showed gains in progression-free survival (PFS). Key details include:
GOG218 — The Gynecologic Oncology Group study evaluated the addition of bevacizumab to standard front-line therapy in 1873 women with newly diagnosed stage III or stage IV epithelial ovarian cancer. Participants were randomized to receive chemotherapy consisting of paclitaxel and carboplatin plus either a placebo, bevacizimab as initiation treatment, or bevacizumab throughout treatment. (N Eng J Med; 2011;365(26):2473-2483). The median PFS was 14.1 months (hazard ratio [HR] = 0.717; 95% confidence interval [CI], 0.625-0.824; P <.001) with bevacizumab throughout, as compared with 11.2 months (HR = 0.908; 95% CI, 0.795- 1.040; P = .16) in the bevacizumab initiation group, and 10.3 months in the control arm.
ICON7 — The Gynaecologic Cancer InterGroup trial randomly assigned 1528 women to receive either carboplatin and paclitaxel, or that regimen plus bevacizumab. Among the participants, 90% had epithelial ovarian cancer and disease burden ranged from 9% with high-risk early-stage disease to 70% at stage IIIC or stage IV (N Engl J Med. 2011;366:2484-2496). At 36 months, PFS was 21.8 months with standard therapy plus bevacizumab (HR = 0.81; 95% CI, 0.70-0.94; P = .004) compared with 20.3 months with standard therapy alone.
Birrer, who was among the key investigators in the GOG218 trial, said the crossover rate in that study likely was about 30% to 50%. “That confounds the overall survival endpoint and, unfortunately, may neutralize any effect of bevacizumab on overall survival for GOG218,” he said.
Production of Avastin in Switzerland. Photo courtesy of Roche.
|Title||Expiration Date||CME Credits|
|Oncology Best Practice™: Expert Perspectives to Incorporate Evidence on PARP Inhibitors into Practice and Optimize the Medical Management of Ovarian Cancer||Oct 31, 2018||1.0|
|Community Practice Connections™: Precision Medicine for Community Oncologists: Assessing the Role of Tumor-Testing Technologies in Cancer Care||Nov 30, 2018||1.0|