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Bevacizumab as adjuvant treatment of colon cancer: updated results from the S-AVANT phase III study by the GERCOR Group

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dc.contributor.authorAndre, T.-
dc.contributor.authorVernerey, D.-
dc.contributor.authorIm, S. A.-
dc.contributor.authorBodoky, G.-
dc.contributor.authorBuzzoni, R.-
dc.contributor.authorReingold, S.-
dc.contributor.authorRivera, F.-
dc.contributor.authorMcKendrick, J.-
dc.contributor.authorScheithauer, W.-
dc.contributor.authorRavit, G.-
dc.contributor.authorFountzilas, G.-
dc.contributor.authorYong, W. P.-
dc.contributor.authorIsaacs, R.-
dc.contributor.authorOsterlund, P.-
dc.contributor.authorLiang, J. T.-
dc.contributor.authorCreemers, G. J.-
dc.contributor.authorRakez, M.-
dc.contributor.authorVan Cutsem, E.-
dc.contributor.authorCunningham, D.-
dc.contributor.authorTabernero, J.-
dc.contributor.authorde Gramont, A.-
dc.date.accessioned2022-03-22T09:25:08Z-
dc.date.available2022-03-22T09:25:08Z-
dc.date.created2020-05-15-
dc.date.created2020-05-15-
dc.date.created2020-05-15-
dc.date.created2020-05-15-
dc.date.issued2020-02-
dc.identifier.citationAnnals of Oncology, Vol.31 No.2, pp.246-256-
dc.identifier.issn0923-7534-
dc.identifier.other100117-
dc.identifier.urihttps://hdl.handle.net/10371/177350-
dc.description.abstractBackground: The bevacizumab-Avastin (R) adjuVANT (AVANT) study did not meet its primary end point of improving disease-free survival (DFS) with the addition of bevacizumab to oxaliplatin-based chemotherapy in stage III colon cancer (CC). We report here the long-term survival results (S-AVANT). Patients and methods: Patients with curatively resected stage III CC were randomly assigned to FOLFOX4, FOLFOX4-bevacizumab, or XELOX-bevacizumab. Results: A total of 2867 patients were randomized: FOLFOX4: n = 955, FOLFOX4-bevacizumab: n = 960, XELOX-bevacizumab: n = 952. With a median of 6.73 years follow-up (interquartile range 5.51-10.54), 672 patients died, of whom 198 (20.7%), 250 (26.0%), and 224 (23.5%) were in the FOLFOX4, FOLFOX4-bevacizumab, and XELOX-bevacizumab arms, respectively. The 10-year overall survival (OS) rates were 74.6%, 67.2%, and 69.9%, (P = 0.003) and 5-year disease-free survival (DFS) rates were 73.2%, 68.5%, and 71.0% (P = 0.174), respectively. OS and DFS hazard ratios were 1.29 [95% confidence interval (CI) 1.07-1.55; P = 0.008] and 1.16 (95% CI 0.99-1.37; P = 0.063) for FOLFOX4-bevacizumab versus FOLFOX4 and 1.15 (95% CI 0.95-1.39; P = 0.147) and 1.1 (95% CI 0.93 -1.29; P = 0.269) for XELOX-bevacizumab versus FOLFOX4, respectively. CC-related deaths (n = 542) occurred in 157 (79.3%) patients receiving FOLFOX4, 205 (82.0%) receiving FOLFOX4-bevacizumab, and 180 (80.4%) receiving XELOX-bevacizumab (P = 0.764), while non-CC-related deaths occurred in 41 (20.7%), 45 (18.0%), and 44 (19.6%) patients, respectively. Cardiovascular-related and sudden deaths during treatment or follow-up were reported in 13 (6.6%), 17 (6.8%), and 14 (6.3%) patients, in the FOLFOX4, FOLFOX4-bevacizuamb, and XELOX-bevacizumab arms, respectively (P = 0.789). Treatment arm, sex, age, histological differentiation, performance status, T/N stages, and localization of primary tumor were independent prognostic factors of OS in stage III. Conclusions: S-AVANT confirms the initial AVANT report. No benefit of the bevacizumab addition to FOLFOX4 adjuvant therapy in patients with stage III CC was observed in terms of DFS with a negative effect in OS, without increase in non-CC related deaths.-
dc.language영어-
dc.publisherOxford University Press-
dc.titleBevacizumab as adjuvant treatment of colon cancer: updated results from the S-AVANT phase III study by the GERCOR Group-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1016/j.annonc.2019.12.006-
dc.citation.journaltitleAnnals of Oncology-
dc.identifier.wosid000516712400012-
dc.identifier.scopusid2-s2.0-85078554434-
dc.citation.endpage256-
dc.citation.number2-
dc.citation.startpage246-
dc.citation.volume31-
dc.identifier.sci000516712400012-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorIm, S. A.-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusSTAGE-II-
dc.subject.keywordPlusOXALIPLATIN-
dc.subject.keywordPlusFLUOROURACIL-
dc.subject.keywordPlusLEUCOVORIN-
dc.subject.keywordPlusTRIAL-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusCAPECITABINE-
dc.subject.keywordPlusIRINOTECAN-
dc.subject.keywordPlusCARCINOMA-
dc.subject.keywordAuthoradjuvant-
dc.subject.keywordAuthorbevacizumab-
dc.subject.keywordAuthorcolon cancer-
dc.subject.keywordAuthorFOLFOX-
dc.subject.keywordAuthorXELOX-
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