J Gynecol Oncol.  2024 Sep;35(5):e99. 10.3802/jgo.2024.35.e99.

First-line bevacizumab plus chemotherapy in Chinese patients with stage III/IV epithelial ovarian cancer, fallopian tube cancer or primary peritoneal cancer: a phase III randomized controlled trial

Affiliations
  • 1Fudan University Shanghai Cancer Center, Shanghai, China
  • 2Sun Yat-sen University Cancer Center, Guangzhou, China
  • 3First Affiliated Hospital of Xi'an Jiaotong University, Xi’an, China
  • 4Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, China
  • 5Xiangya Hospital Central South University, Changsha, China
  • 6Nanjing Drum Tower Hospital, Nanjing, China
  • 7Nantong Tumor Hospital, Nantong, China
  • 8Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, China
  • 9Guangxi Medical University Affiliated Tumor Hospital & Oncology Medical College, Nanning, China
  • 10The First Hospital of Jilin University, Changchun, China
  • 11Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China
  • 12Cancer Hospital of the University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Hangzhou, China
  • 13Harbin Medical University Cancer Hospital, Harbin, China
  • 14Fujian Cancer Hospital, Fuzhou, China
  • 15Jilin Cancer Hospital, Changchun, China
  • 16Tianjin Medical University General Hospital, Tianjin, China
  • 17F. Hoffmann-La Roche Ltd, Basel, Switzerland
  • 18Roche Product Development, Shanghai, China

Abstract


Objective
First-line bevacizumab plus carboplatin and paclitaxel (CP) is approved for stage III/IV ovarian cancer treatment following initial surgical resection, based on global phase III GOG-0218 and ICON7 trials. This study evaluated the efficacy and safety of bevacizumab + CP as first-line ovarian cancer therapy in Chinese patients.
Methods
Patients with newly diagnosed, International Federation of Gynecology and Obstetrics (FIGO) stage III/IV epithelial ovarian, fallopian tube, or primary peritoneal cancer post-primary surgery were randomized 1:1 to receive 6 cycles of CP with bevacizumab/ placebo, followed by bevacizumab/placebo maintenance until unacceptable toxicity or disease progression. Primary endpoint was investigator-assessed progression-free survival (PFS). Stratification factors were FIGO stage and debulking status (stage III optimally debulked vs stage III suboptimally debulked vs stage IV) and Eastern Cooperative Oncology Group performance status (0 vs 1 or 2).
Results
Of randomized patients, 51 received bevacizumab + CP and 49 received placebo + CP. Median PFS was 22.6 months with bevacizumab + CP (95% confidence interval [CI]=18.6, not estimable) and 12.3 months (95% CI=9.5, 15.0) with placebo + CP (stratified hazard ratio=0.30; 95% CI=0.17, 0.53). Treatment-related grade 3/4 adverse events occurred in 46 of 49 (94%) patients receiving bevacizumab + CP, and 34 of 50 (68%) receiving placebo + CP.
Conclusion
Bevacizumab + CP showed clinically meaningful improvement in PFS vs placebo + CP, consistent with GOG-0218 results. Safety data were aligned with the known bevacizumab safety profile. These results support first-line bevacizumab + CP therapy in Chinese patients with ovarian cancer.

Keyword

Bevacizumab; Chemotherapy; Chinese; Ovarian Cancer
Full Text Links
  • JGO
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2025 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr