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Pembrolizumab or pembrolizumab plus chemotherapy versus standard of care chemotherapy in patients with advanced gastric or gastroesophageal junction adenocarcinoma: Asian subgroup analysis of KEYNOTE-062

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dc.contributor.authorSatake, Hironaga-
dc.contributor.authorLee, Keun-Wook-
dc.contributor.authorChung, Hyun Cheol-
dc.contributor.authorLee, Jeeyun-
dc.contributor.authorYamaguchi, Kensei-
dc.contributor.authorChen, Jen-Shi-
dc.contributor.authorYoshikawa, Takaki-
dc.contributor.authorAmagai, Kenji-
dc.contributor.authorYeh, Kun-Huei-
dc.contributor.authorGoto, Masahiro-
dc.contributor.authorChao, Yee-
dc.contributor.authorLam, Ka-On-
dc.contributor.authorHan, Shi Rong-
dc.contributor.authorShiratori, Shinichi-
dc.contributor.authorShah, Sukrut-
dc.contributor.authorShitara, Kohei-
dc.date.accessioned2024-03-27T00:52:18Z-
dc.date.available2024-03-27T00:52:18Z-
dc.date.created2023-04-14-
dc.date.issued2023-03-
dc.identifier.issn0368-2811-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198753-
dc.description.abstractObjective: First-line pembrolizumab with/without chemotherapy versus chemotherapy was evaluated in programmed death ligand 1 combined positive score >= 1, locally advanced/unresectable or metastatic gastric cancer/gastrooesophageal junction cancer in the KEYNOTE-062 study. We present results for patients enrolled in Asia.Methods: Eligible patients were randomly assigned 1:1:1 to pembrolizumab 200 mg, pembrolizumab plus chemotherapy (cisplatin + 5-fluorouracil or capecitabine) or placebo plus chemotherapy Q3W. End points included overall survival (primary) in combined positive score >= 1 and combined positive score >= 10 populations and safety and tolerability (secondary).Results: A total of 187 patients were enrolled in Asia (pembrolizumab, n = 62; pembrolizumab plus chemotherapy, n = 64; chemotherapy, n = 61). Compared with the global population, higher proportions of patients had Eastern Cooperative Oncology Group performance status 0 and a diagnosis of stomach cancer. In the programmed death ligand 1 combined positive score >= 1 population, median overall survival was numerically longer with pembrolizumab versus chemotherapy (22.7 vs 13.8 months; hazard ratio, 0.54; 95% confidence interval, 0.35-0.82) and pembrolizumab plus chemotherapy versus chemotherapy (16.5 vs 13.8 months; hazard ratio, 0.78; 95% confidence interval, 0.53-1.16). In the programmed death ligand 1 combined positive score >= 10 population, median overall survival was also numerically longer with pembrolizumab versus chemotherapy (28.5 vs 14.8 months; hazard ratio, 0.43; 95% confidence interval, 0.21-0.89) and pembrolizumab plus chemotherapy versus chemotherapy (17.5 vs 14.8 months; hazard ratio, 0.86; 95% confidence interval, 0.45-1.64). The grade 3-5 treatment-related adverse event rate was 19.4%, 75.8% and 64.9% for patients receiving pembrolizumab, pembrolizumab plus chemotherapy and chemotherapy, respectively.Conclusions: This post hoc analysis showed pembrolizumab monotherapy was associated with numerically improved overall survival and a favourable tolerability profile versus chemotherapy in Asians with programmed death ligand 1-positive advanced gastric cancer/gastrooesophageal junction cancer.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherOxford University Press-
dc.relation.isPartOfJapanese Journal of Clinical Oncology-
dc.relation.isPartOfJAPANESE JOURNAL OF CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titlePembrolizumab or pembrolizumab plus chemotherapy versus standard of care chemotherapy in patients with advanced gastric or gastroesophageal junction adenocarcinoma: Asian subgroup analysis of KEYNOTE-062-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSatake, Hironaga-
dc.contributor.googleauthorLee, Keun-Wook-
dc.contributor.googleauthorChung, Hyun Cheol-
dc.contributor.googleauthorLee, Jeeyun-
dc.contributor.googleauthorYamaguchi, Kensei-
dc.contributor.googleauthorChen, Jen-Shi-
dc.contributor.googleauthorYoshikawa, Takaki-
dc.contributor.googleauthorAmagai, Kenji-
dc.contributor.googleauthorYeh, Kun-Huei-
dc.contributor.googleauthorGoto, Masahiro-
dc.contributor.googleauthorChao, Yee-
dc.contributor.googleauthorLam, Ka-On-
dc.contributor.googleauthorHan, Shi Rong-
dc.contributor.googleauthorShiratori, Shinichi-
dc.contributor.googleauthorShah, Sukrut-
dc.contributor.googleauthorShitara, Kohei-
dc.identifier.doi10.1093/jjco/hyac188-
dc.relation.journalcodeJ01207-
dc.identifier.eissn1465-3621-
dc.identifier.pmid36533429-
dc.subject.keywordpembrolizumab-
dc.subject.keywordchemotherapy-
dc.subject.keywordgastric cancer-
dc.subject.keywordgastrooesophageal junction cancer-
dc.subject.keywordAsian patients-
dc.contributor.alternativeNameChung, Hyun Cheol-
dc.contributor.affiliatedAuthorChung, Hyun Cheol-
dc.identifier.scopusid2-s2.0-85149999892-
dc.identifier.wosid000900386800001-
dc.citation.volume53-
dc.citation.number3-
dc.citation.startPage221-
dc.citation.endPage229-
dc.identifier.bibliographicCitationJapanese Journal of Clinical Oncology, Vol.53(3) : 221-229, 2023-03-
dc.identifier.rimsid78458-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorpembrolizumab-
dc.subject.keywordAuthorchemotherapy-
dc.subject.keywordAuthorgastric cancer-
dc.subject.keywordAuthorgastrooesophageal junction cancer-
dc.subject.keywordAuthorAsian patients-
dc.subject.keywordPlusOPEN-LABEL-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusOXALIPLATIN-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusS-1-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalResearchAreaOncology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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