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Bevacizumab in combination with chemotherapy as first-line therapy in advanced gastric cancer: a randomized, double-blind, placebo-controlled phase III study.

DC Field Value Language
dc.contributor.author라선영-
dc.date.accessioned2014-12-20T17:49:14Z-
dc.date.available2014-12-20T17:49:14Z-
dc.date.issued2011-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/95315-
dc.description.abstractPURPOSE: The Avastin in Gastric Cancer (AVAGAST) trial was a multinational, randomized, placebo-controlled trial designed to evaluate the efficacy of adding bevacizumab to capecitabine-cisplatin in the first-line treatment of advanced gastric cancer. PATIENTS AND METHODS: Patients received bevacizumab 7.5 mg/kg or placebo followed by cisplatin 80 mg/m(2) on day 1 plus capecitabine 1,000 mg/m(2) twice daily for 14 days every 3 weeks. Fluorouracil was permitted in patients unable to take oral medications. Cisplatin was given for six cycles; capecitabine and bevacizumab were administered until disease progression or unacceptable toxicity. The primary end point was overall survival (OS). Log-rank test was used to test the OS difference. RESULTS: In all, 774 patients were enrolled; 387 were assigned to each treatment group (intention-to-treat population), and 517 deaths were observed. Median OS was 12.1 months with bevacizumab plus fluoropyrimidine-cisplatin and 10.1 months with placebo plus fluoropyrimidine-cisplatin (hazard ratio 0.87; 95% CI, 0.73 to 1.03; P = .1002). Both median progression-free survival (6.7 v 5.3 months; hazard ratio, 0.80; 95% CI, 0.68 to 0.93; P = .0037) and overall response rate (46.0% v 37.4%; P = .0315) were significantly improved with bevacizumab versus placebo. Preplanned subgroup analyses revealed regional differences in efficacy outcomes. The most common grade 3 to 5 adverse events were neutropenia (35%, bevacizumab plus fluoropyrimidine-cisplatin; 37%, placebo plus fluoropyrimidine-cisplatin), anemia (10% v 14%), and decreased appetite (8% v 11%). No new bevacizumab-related safety signals were identified. CONCLUSION: Although AVAGAST did not reach its primary objective, adding bevacizumab to chemotherapy was associated with significant increases in progression-free survival and overall response rate in the first-line treatment of advanced gastric cancer.-
dc.description.statementOfResponsibilityopen-
dc.format.extent3968~3976-
dc.relation.isPartOfJOURNAL OF CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAntibodies, Monoclonal, Humanized/administration & dosage-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols/therapeutic use*-
dc.subject.MESHBevacizumab-
dc.subject.MESHCapecitabine-
dc.subject.MESHCisplatin/administration & dosage-
dc.subject.MESHDeoxycytidine/administration & dosage-
dc.subject.MESHDeoxycytidine/analogs & derivatives-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHDouble-Blind Method-
dc.subject.MESHFluorouracil/administration & dosage-
dc.subject.MESHFluorouracil/analogs & derivatives-
dc.subject.MESHHumans-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPlacebos-
dc.subject.MESHStomach Neoplasms/drug therapy*-
dc.subject.MESHSurvival Rate-
dc.subject.MESHYoung Adult-
dc.titleBevacizumab in combination with chemotherapy as first-line therapy in advanced gastric cancer: a randomized, double-blind, placebo-controlled phase III study.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorAtsushi Ohtsu-
dc.contributor.googleauthorManish A. Shah-
dc.contributor.googleauthorEric Van Cutsem-
dc.contributor.googleauthorSun Young Rha-
dc.contributor.googleauthorAkira Sawaki-
dc.contributor.googleauthorSook Ryun Park-
dc.contributor.googleauthorHo Yeong Lim-
dc.contributor.googleauthorYasuhide Yamada-
dc.contributor.googleauthorJian Wu-
dc.contributor.googleauthorBernd Langer-
dc.contributor.googleauthorMichal Starnawski-
dc.contributor.googleauthorYoon-Koo Kang-
dc.identifier.doi10.1200/JCO.2011.36.2236-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01316-
dc.relation.journalcodeJ01331-
dc.identifier.eissn1527-7755-
dc.identifier.pmid21844504-
dc.identifier.urlhttp://jco.ascopubs.org/content/29/30/3968.long-
dc.contributor.alternativeNameRha, Sun Young-
dc.contributor.affiliatedAuthorRha, Sun Young-
dc.rights.accessRightsnot free-
dc.citation.volume29-
dc.citation.number30-
dc.citation.startPage3968-
dc.citation.endPage3976-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL ONCOLOGY, Vol.29(30) : 3968-3976, 2011-
dc.identifier.rimsid31400-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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