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Use of archival versus newly collected tumor samples for assessing PD-L1 expression and overall survival: an updated analysis of KEYNOTE-010 trial

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dc.contributor.authorHerbst, R. S.-
dc.contributor.authorBaas, P.-
dc.contributor.authorPerez-Gracia, J. L.-
dc.contributor.authorFelip, E.-
dc.contributor.authorKim, D. -W.-
dc.contributor.authorHan, J. -Y.-
dc.contributor.authorMolina, J. R.-
dc.contributor.authorKim, J. -H.-
dc.contributor.authorArvis, C. Dubos-
dc.contributor.authorAhn, M. -J.-
dc.contributor.authorMajem, M.-
dc.contributor.authorFidler, M. J.-
dc.contributor.authorSurmont, V.-
dc.contributor.authorde Castro, G., Jr.-
dc.contributor.authorGarrido, M.-
dc.contributor.authorShentu, Y.-
dc.contributor.authorEmancipator, K.-
dc.contributor.authorSamkari, A.-
dc.contributor.authorJensen, E. H.-
dc.contributor.authorLubiniecki, G. M.-
dc.contributor.authorGaron, E. B.-
dc.date.accessioned2021-01-31T08:07:40Z-
dc.date.available2021-01-31T08:07:40Z-
dc.date.created2020-04-27-
dc.date.created2020-04-27-
dc.date.issued2019-02-
dc.identifier.citationAnnals of Oncology, Vol.30 No.2, pp.281-289-
dc.identifier.issn0923-7534-
dc.identifier.other97573-
dc.identifier.urihttps://hdl.handle.net/10371/171831-
dc.description.abstractBackground: In KEYNOTE-010, pembrolizumab versus docetaxel improved overall survival (OS) in patients with programmed death-1 protein (PD)-L1-positive advanced non-small-cell lung cancer (NSCLC). A prespecified exploratory analysis compared outcomes in patients based on PD-L1 expression in archival versus newly collected tumor samples using recently updated survival data. Patients and methods: PD-L1 was assessed centrally by immunohistochemistry (22C3 antibody) in archival or newly collected tumor samples. Patients received pembrolizumab 2 or 10 mg/kg Q3W or docetaxel 75 mg/m2 Q3W for 24 months or until progression/intolerable toxicity/other reason. Response was assessed by RECIST v1.1 every 9 weeks, survival every 2 months. Primary end points were OS and progression-free survival (PFS) in tumor proportion score (TPS) 50% and 1%; pembrolizumab doses were pooled in this analysis. Results: At date cut-off of 24 March 2017, median follow-up was 31 months (range 23-41) representing 18 additional months of follow-up from the primary analysis. Pembrolizumab versus docetaxel continued to improve OS in patients with previously treated, PD-L1-expressing advanced NSCLC; hazard ratio (HR) was 0.66 [95% confidence interval (CI): 0.57, 0.77]. Of 1033 patients analyzed, 455(44%) were enrolled based on archival samples and 578 (56%) on newly collected tumor samples. Approximately 40% of archival samples and 45% of newly collected tumor samples were PD-L1 TPS 50%. For TPS 50%, the OS HRs were 0.64 (95% CI: 0.45, 0.91) and 0.40 (95% CI: 0.28, 0.56) for archival and newly collected samples, respectively. In patients with TPS 1%, OS HRs were 0.74 (95% CI: 0.59, 0.93) and 0.59 (95% CI: 0.48, 0.73) for archival and newly collected samples, respectively. In TPS 50%, PFS HRs were similar across archival [0.63 (95% CI: 0.45, 0.89)] and newly collected samples [0.53 (95% CI: 0.38, 0.72)]. In patients with TPS 1%, PFS HRs were similar across archival [0.82 (95% CI: 0.66, 1.02)] and newly collected samples [0.83 (95% CI: 0.68, 1.02)]. Conclusion: Pembrolizumab continued to improve OS over docetaxel in intention to treat population and in subsets of patients with newly collected and archival samples.-
dc.language영어-
dc.publisherOxford University Press-
dc.titleUse of archival versus newly collected tumor samples for assessing PD-L1 expression and overall survival: an updated analysis of KEYNOTE-010 trial-
dc.typeArticle-
dc.contributor.AlternativeAuthor김동완-
dc.identifier.doi10.1093/annonc/mdy545-
dc.citation.journaltitleAnnals of Oncology-
dc.identifier.wosid000463940300016-
dc.identifier.scopusid2-s2.0-85061979211-
dc.citation.endpage289-
dc.citation.number2-
dc.citation.startpage281-
dc.citation.volume30-
dc.identifier.sci000463940300016-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, D. -W.-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusIMMUNOHISTOCHEMISTRY-
dc.subject.keywordPlusPEMBROLIZUMAB-
dc.subject.keywordPlusB7-H1-
dc.subject.keywordPlusGAMMA-
dc.subject.keywordAuthorpembrolizumab-
dc.subject.keywordAuthortumor samples-
dc.subject.keywordAuthorPD-L1 expression-
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