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Everolimus for Previously Treated Advanced Gastric Cancer: Results of the Randomized, Double-Blind, Phase III GRANITE-1 Study

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dc.contributor.author정현철-
dc.date.accessioned2014-12-18T09:54:01Z-
dc.date.available2014-12-18T09:54:01Z-
dc.date.issued2013-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/89039-
dc.description.abstractPURPOSE: The oral mammalian target of rapamycin inhibitor everolimus demonstrated promising efficacy in a phase II study of pretreated advanced gastric cancer. This international, double-blind, phase III study compared everolimus efficacy and safety with that of best supportive care (BSC) in previously treated advanced gastric cancer. PATIENTS AND METHODS: Patients with advanced gastric cancer that progressed after one or two lines of systemic chemotherapy were randomly assigned to everolimus 10 mg/d (assignment schedule: 2:1) or matching placebo, both given with BSC. Randomization was stratified by previous chemotherapy lines (one v two) and region (Asia v rest of the world [ROW]). Treatment continued until disease progression or intolerable toxicity. Primary end point was overall survival (OS). Secondary end points included progression-free survival (PFS), overall response rate, and safety. RESULTS: Six hundred fifty-six patients (median age, 62.0 years; 73.6% male) were enrolled. Median OS was 5.4 months with everolimus and 4.3 months with placebo (hazard ratio, 0.90; 95% CI, 0.75 to 1.08; P = .124). Median PFS was 1.7 months and 1.4 months in the everolimus and placebo arms, respectively (hazard ratio, 0.66; 95% CI, 0.56 to 0.78). Common grade 3/4 adverse events included anemia, decreased appetite, and fatigue. The safety profile was similar in patients enrolled in Asia versus ROW. CONCLUSION: Compared with BSC, everolimus did not significantly improve overall survival for advanced gastric cancer that progressed after one or two lines of previous systemic chemotherapy. The safety profile observed for everolimus was consistent with that observed for everolimus in other cancers.-
dc.description.statementOfResponsibilityopen-
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.titleEverolimus for Previously Treated Advanced Gastric Cancer: Results of the Randomized, Double-Blind, Phase III GRANITE-1 Study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorAtsushi Ohtsu-
dc.contributor.googleauthorJaffer A. Ajani-
dc.contributor.googleauthorYu-Xian Bai-
dc.contributor.googleauthorYung-Jue Bang-
dc.contributor.googleauthorHyun-Cheol Chung-
dc.contributor.googleauthorHong-Ming Pan-
dc.contributor.googleauthorTarek Sahmoud-
dc.contributor.googleauthorLin Shen-
dc.contributor.googleauthorKun-Huei Yeh-
dc.contributor.googleauthorKeisho Chin-
dc.contributor.googleauthorKei Muro-
dc.contributor.googleauthorYeul Hong Kim-
dc.contributor.googleauthorDavid Ferry-
dc.contributor.googleauthorNiall C. Tebbutt-
dc.contributor.googleauthorSalah-Eddin Al-Batran-
dc.contributor.googleauthorHeind Smith-
dc.contributor.googleauthorChiara Costantini-
dc.contributor.googleauthorSyed Rizvi-
dc.contributor.googleauthorDavid Lebwohl-
dc.contributor.googleauthorEric Van Cutsem-
dc.identifier.doi10.1200/JCO.2012.48.3552-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03773-
dc.relation.journalcodeJ01331-
dc.identifier.urlhttp://jco.ascopubs.org/content/31/31/3935-
dc.contributor.alternativeNameChung, Hyun Cheol-
dc.contributor.affiliatedAuthorChung, Hyun Cheol-
dc.rights.accessRightsnot free-
dc.citation.volume31-
dc.citation.number31-
dc.citation.startPage3935-
dc.citation.endPage3943-
dc.identifier.bibliographicCitationJournal of Clinical Oncology, Vol.31(31) : 3935-3943, 2013-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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