Optimal Treatment Duration of Bevacizumab as Front-Line Therapy for Advanced Ovarian Cancer: AGO-OVAR 17 BOOST/GINECO OV118/ENGOT Ov-15 Open-Label Randomized Phase III Trial.

TitleOptimal Treatment Duration of Bevacizumab as Front-Line Therapy for Advanced Ovarian Cancer: AGO-OVAR 17 BOOST/GINECO OV118/ENGOT Ov-15 Open-Label Randomized Phase III Trial.
Publication TypeJournal Article
Year of Publication2023
AuthorsPfisterer, J, Joly, F, Kristensen, G, Rau, J, Mahner, S, Pautier, P, El-Balat, A, Kurtz, J-E, Canzler, U, Sehouli, J, Heubner, ML, Hartkopf, AD, Baumann, K, Hasenburg, A, Hanker, LC, Belau, A, Schmalfeldt, B, Denschlag, D, Park-Simon, T-W, Selle, F, Jackisch, C, Burges, A, Lück, H-J, Emons, G, Meier, W, Gropp-Meier, M, Schröder, W, de Gregorio, N, Hilpert, F, Harter, P
JournalJ Clin Oncol
Volume41
Issue4
Pagination893-902
Date Published2023 Feb 01
ISSN1527-7755
KeywordsAntineoplastic Combined Chemotherapy Protocols, Bevacizumab, Carboplatin, Carcinoma, Ovarian Epithelial, Duration of Therapy, Female, Humans, Ovarian Neoplasms, Paclitaxel, Peritoneal Neoplasms
Abstract

PURPOSE: To compare standard versus extended duration of bevacizumab treatment in combination with front-line chemotherapy in women with newly diagnosed stage IIB-IV ovarian cancer.METHODS: In this multicenter, open-label, randomized phase III trial (ClinicalTrials.gov identifier: NCT01462890), patients with newly diagnosed International Federation of Gynecology and Obstetrics stage IIB-IV epithelial ovarian, fallopian tube, or peritoneal cancer underwent primary cytoreductive surgery followed by six cycles of chemotherapy (paclitaxel 175 mg/m plus carboplatin area under the curve 5 once every 3 weeks) and bevacizumab (15 mg/kg once every 3 weeks). Patients were randomly assigned 1:1 to receive bevacizumab for either 15 or 30 months, stratified by International Federation of Gynecology and Obstetrics stage/residual tumor. The primary end point was investigator-assessed progression-free survival (PFS) according to RECIST version 1.1. Secondary end points included overall survival (OS), safety, and tolerability.RESULTS: Between November 11, 2011, and August 6, 2013, 927 women were randomly assigned. There was no difference in PFS between treatment arms (hazard ratio, 0.99; 95% CI, 0.85 to 1.15; unstratified log-rank = .90). Median PFS was 24.2 versus 26.0 months with standard versus extended duration of bevacizumab, respectively; restricted mean PFS was 39.5 versus 39.3 months, respectively. There was no OS difference between treatment arms (hazard ratio, 1.04; 95% CI, 0.87 to 1.23; = .68). Serious/nonserious adverse events of special interest occurred in 29% versus 34% of patients in the standard versus experimental arms, respectively, and were consistent with the known safety profile of standard bevacizumab.CONCLUSION: Longer treatment duration with bevacizumab for up to 30 months did not improve PFS or OS in patients with primary epithelial ovarian, fallopian tube, or peritoneal cancer. A bevacizumab treatment duration of 15 months remains the standard of care.

DOI10.1200/JCO.22.01010
Alternate JournalJ Clin Oncol
PubMed ID36332161