TY - JOUR
T1 - Secondary surgical cytoreduction for recurrent ovarian cancer
AU - Coleman, Robert L.
AU - Spirtos, Nick M.
AU - Enserro, Danielle
AU - Herzog, Thomas J.
AU - Sabbatini, Paul
AU - Armstrong, Deborah K.
AU - Weon Kim, Jae
AU - Yoon Park, Sang
AU - Gie Kim, Byoung
AU - Hyun Nam, Joo
AU - Fujiwara, Keiichi
AU - Walker, Joan L.
AU - Casey, Ann C.
AU - Secord, Angeles Alvarez
AU - Rubin, Steve
AU - Chan, John K.
AU - DiSilvestro, Paul
AU - Davidson, Susan A.
AU - Cohn, David E.
AU - Tewari, Krishnansu S.
AU - Basen-Engquist, Karen
AU - Huang, Helen Q.
AU - Brady, Mark F.
AU - Mannel, Robert S.
N1 - Funding Information:
Supported by National Cancer Institute (NCI) grants to the Gynecologic Oncology Group (GOG) Administrative Office (CA 27469), the GOG Statistical Office (CA 37517), NRG Oncology (1U10 CA180822), and the NRG Network Operations Center (U10CA180868) and in part by the National Institutes of Health/ NCI under award number P30CA016672 (the investigators used the clinical research shared resource). Roche/Genentech supported the NCI cooperative research and development agreement enabling this trial. Dr. Coleman is supported in part by the Ann Rife Cox Chair in Gynecology and the Judy Reis/Albert Pisani, M.D., Ovarian Cancer Research Fund.
Funding Information:
The trial was designed by the authors and supported by the Cancer Therapy Evaluation Program (CTEP) of the National Cancer Institute (NCI). The data were collected and analyzed and the manuscript was written by the authors, who vouch for the completeness and accuracy of the data and for the adherence of the trial to the protocol. All the patients provided written informed consent. Genentech provided bevacizumab and supplemental funding support to the GOG through a cooperative research and development agreement with the NCI but played no role in the collection or analysis of data or its interpretation.
Publisher Copyright:
© 2019 Massachussetts Medical Society. All rights reserved.
PY - 2019/11/14
Y1 - 2019/11/14
N2 - BACKGROUND Secondary surgical cytoreduction in women with platinum-sensitive, recurrent epithelial ovarian, primary peritoneal, or fallopian-Tube ("ovarian") cancer is widely practiced but has not been evaluated in phase 3 investigation. METHODS We randomly assigned patients with recurrent ovarian cancer who had received one previous therapy, had an interval during which no platinum-based chemotherapy was used (platinum-free interval) of 6 months or more, and had investigator-determined resectable disease (to no macroscopic residual disease) to undergo secondary surgical cytoreduction and then receive platinum-based chemotherapy or to receive platinumbased chemotherapy alone. Adjuvant chemotherapy (paclitaxel carboplatin or gemcitabine carboplatin) and use of bevacizumab were at the discretion of the investigator. The primary end point was overall survival. RESULTS A total of 485 patients underwent randomization, 240 to secondary cytoreduction before chemotherapy and 245 to chemotherapy alone. The median follow-up was 48.1 months. Complete gross resection was achieved in 67% of the patients assigned to surgery who underwent the procedure. Platinum-based chemotherapy with bevacizumab followed by bevacizumab maintenance was administered to 84% of the patients overall and was equally distributed between the two groups. The hazard ratio for death (surgery vs. no surgery) was 1.29 (95% confidence interval [CI], 0.97 to 1.72; P = 0.08), which corresponded to a median overall survival of 50.6 months and 64.7 months, respectively. Adjustment for platinum-free interval and chemotherapy choice did not alter the effect. The hazard ratio for disease progression or death (surgery vs. no surgery) was 0.82 (95% CI, 0.66 to 1.01; median progression-free survival, 18.9 months and 16.2 months, respectively). Surgical morbidity at 30 days was 9%; 1 patient (0.4%) died from postoperative complications. Patient-reported quality of life decreased significantly after surgery but did not differ significantly between the two groups after recovery. CONCLUSIONS In this trial involving patients with platinum-sensitive, recurrent ovarian cancer, secondary surgical cytoreduction followed by chemotherapy did not result in longer overall survival than chemotherapy alone. (Funded by the National Cancer Institute and others; GOG-0213 ClinicalTrials.gov number, NCT00565851.).
AB - BACKGROUND Secondary surgical cytoreduction in women with platinum-sensitive, recurrent epithelial ovarian, primary peritoneal, or fallopian-Tube ("ovarian") cancer is widely practiced but has not been evaluated in phase 3 investigation. METHODS We randomly assigned patients with recurrent ovarian cancer who had received one previous therapy, had an interval during which no platinum-based chemotherapy was used (platinum-free interval) of 6 months or more, and had investigator-determined resectable disease (to no macroscopic residual disease) to undergo secondary surgical cytoreduction and then receive platinum-based chemotherapy or to receive platinumbased chemotherapy alone. Adjuvant chemotherapy (paclitaxel carboplatin or gemcitabine carboplatin) and use of bevacizumab were at the discretion of the investigator. The primary end point was overall survival. RESULTS A total of 485 patients underwent randomization, 240 to secondary cytoreduction before chemotherapy and 245 to chemotherapy alone. The median follow-up was 48.1 months. Complete gross resection was achieved in 67% of the patients assigned to surgery who underwent the procedure. Platinum-based chemotherapy with bevacizumab followed by bevacizumab maintenance was administered to 84% of the patients overall and was equally distributed between the two groups. The hazard ratio for death (surgery vs. no surgery) was 1.29 (95% confidence interval [CI], 0.97 to 1.72; P = 0.08), which corresponded to a median overall survival of 50.6 months and 64.7 months, respectively. Adjustment for platinum-free interval and chemotherapy choice did not alter the effect. The hazard ratio for disease progression or death (surgery vs. no surgery) was 0.82 (95% CI, 0.66 to 1.01; median progression-free survival, 18.9 months and 16.2 months, respectively). Surgical morbidity at 30 days was 9%; 1 patient (0.4%) died from postoperative complications. Patient-reported quality of life decreased significantly after surgery but did not differ significantly between the two groups after recovery. CONCLUSIONS In this trial involving patients with platinum-sensitive, recurrent ovarian cancer, secondary surgical cytoreduction followed by chemotherapy did not result in longer overall survival than chemotherapy alone. (Funded by the National Cancer Institute and others; GOG-0213 ClinicalTrials.gov number, NCT00565851.).
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U2 - 10.1056/NEJMoa1902626
DO - 10.1056/NEJMoa1902626
M3 - Article
C2 - 31722153
AN - SCOPUS:85075078979
SN - 0028-4793
VL - 381
SP - 1929
EP - 1939
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 20
ER -