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Efficacy of Pembrolizumab Monotherapy for Advanced Gastric/Gastroesophageal Junction Cancer with Programmed Death Ligand 1 Combined Positive Score >= 10

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dc.contributor.authorWainberg, Zev A.-
dc.contributor.authorFuchs, Charles S.-
dc.contributor.authorTabernero, Josep-
dc.contributor.authorShitara, Kohei-
dc.contributor.authorMuro, Kei-
dc.contributor.authorVan Cutsem, Eric-
dc.contributor.authorBang, Yung-Jue-
dc.contributor.authorChung, Hyun Cheol-
dc.contributor.authorYamaguchi, Kensei-
dc.contributor.authorVarga, Eniko-
dc.contributor.authorChen, Jen-Shi-
dc.contributor.authorHochhauser, Daniel-
dc.contributor.authorThuss-Patience, Peter-
dc.contributor.authorAl-Batran, Salah-Eddin-
dc.contributor.authorGarrido, Marcelo-
dc.contributor.authorKher, Uma-
dc.contributor.authorShih, Chie-Schin-
dc.contributor.authorShah, Sukrut-
dc.contributor.authorBhagia, Pooja-
dc.contributor.authorChao, Joseph-
dc.date.accessioned2021-09-29T01:54:09Z-
dc.date.available2021-09-29T01:54:09Z-
dc.date.created2021-07-06-
dc.date.issued2021-04-
dc.identifier.issn1078-0432-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/184607-
dc.description.abstractPurpose: Pembrolizumab demonstrated efficacy in PD-L1-positive [combined positive score (CPS) >= 1] advanced gastric/gastro-esophageal junction (G/GEJ) cancer in the first-, second-, and third-line setting in KEYNOTE-062, KEYNOTE-061, and KEYNOTE-059, respectively. To better delineate the specificity of CPS as a predictor of dinical outcomes, we analyzed pembrolizumab efficacy in patients with CPS >= 10 in these trials. Patients and Methods: Included were patients with CPS >= 10 tumors from KEYNOTE-059 cohort I (pembrolizumab, n = 46; post hoc), KEYNOTE-061 (pembrolizumab, n = 53; chemotherapy, n = 55; post hoc), and KEYNOTE-062 (pembrolizumab, n = 92; chemotherapy, n = 90; primary). Efficacy outcomes were overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and duration of response (DOR). Results: In KEYNOTE-059, median follow-up was 6 months, median OS was 8 months [95% confidence interval (CI), 5.8-11.1], ORR was 17%, and median (range) DOR was 21 months (3+ to 35+). In KEYNOTE-061, median follow-up was 9 months, median OS (pembrolizumab vs. chemotherapy) was 10 versus 8 months (HR, 0.64; 95% CI, 0.41-1.02), median PFS was 3 months versus 3 months (HR, 0.86; 95% CI, 056-1.33), ORR was 25% versus 9%, and median (range) DOR was not reached (4 to 26+ months) versus 7 months (3-7). In KEYNOTE-062, median follow-up was 11 months, median OS (pembrolizumab vs. chemotherapy) was 17 months versus 11 months (HR, 0.69; 95% CI, 0.49-0.97), median PFS was 3 months versus 6 months (HR, 1.09, 95% CI; 0.79-1.49), ORR was 25% versus 38%, and median (range) DOR was 19 months (1+ to 34+) versus 7 months (2+ to 30+). Conclusions: This comprehensive analysis showed consistent improvements toward more favorable clinical outcomes with pembrolizumab across lines of therapy in patients with CPS >= 10 G/GEJ cancer.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Association for Cancer Research-
dc.relation.isPartOfCLINICAL CANCER RESEARCH-
dc.relation.isPartOfCLINICAL CANCER RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleEfficacy of Pembrolizumab Monotherapy for Advanced Gastric/Gastroesophageal Junction Cancer with Programmed Death Ligand 1 Combined Positive Score >= 10-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorWainberg, Zev A.-
dc.contributor.googleauthorFuchs, Charles S.-
dc.contributor.googleauthorTabernero, Josep-
dc.contributor.googleauthorShitara, Kohei-
dc.contributor.googleauthorMuro, Kei-
dc.contributor.googleauthorVan Cutsem, Eric-
dc.contributor.googleauthorBang, Yung-Jue-
dc.contributor.googleauthorChung, Hyun Cheol-
dc.contributor.googleauthorYamaguchi, Kensei-
dc.contributor.googleauthorVarga, Eniko-
dc.contributor.googleauthorChen, Jen-Shi-
dc.contributor.googleauthorHochhauser, Daniel-
dc.contributor.googleauthorThuss-Patience, Peter-
dc.contributor.googleauthorAl-Batran, Salah-Eddin-
dc.contributor.googleauthorGarrido, Marcelo-
dc.contributor.googleauthorKher, Uma-
dc.contributor.googleauthorShih, Chie-Schin-
dc.contributor.googleauthorShah, Sukrut-
dc.contributor.googleauthorBhagia, Pooja-
dc.contributor.googleauthorChao, Joseph-
dc.identifier.doi10.1158/1078-0432.CCR-20-2980-
dc.relation.journalcodeJ00564-
dc.contributor.alternativeNameChung, Hyun Cheol-
dc.contributor.affiliatedAuthorChung, Hyun Cheol-
dc.identifier.scopusid2-s2.0-85100918894-
dc.identifier.wosid000636977600014-
dc.citation.volume27-
dc.citation.number7-
dc.citation.startPage1923-
dc.citation.endPage1931-
dc.identifier.bibliographicCitationCLINICAL CANCER RESEARCH, Vol.27(7) : 1923-1931, 2021-04-
dc.identifier.rimsid70729-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.type.docTypeArticle-
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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