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Dostarlimab or pembrolizumab plus chemotherapy in previously untreated metastatic non-squamous non-small cell lung cancer: the randomized PERLA phase II trial

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dc.contributor.authorLim, Sun Min-
dc.contributor.authorPeters, Solange-
dc.contributor.authorGranados, Ana Laura Ortega-
dc.contributor.authorPinto, Gustavo dix Junqueira-
dc.contributor.authorFuentes, Christian Sebastian-
dc.contributor.authorLo Russo, Giuseppe-
dc.contributor.authorSchenker, Michael-
dc.contributor.authorAhn, Jin Seok-
dc.contributor.authorReck, Martin-
dc.contributor.authorSzijgyarto, Zsolt-
dc.contributor.authorHuseinovic, Neda-
dc.contributor.authorZografos, Eleftherios-
dc.contributor.authorBuss, Elena-
dc.contributor.authorStjepanovic, Neda-
dc.contributor.authorODonnell, Sean-
dc.contributor.authorde Marinis, Filippo-
dc.date.accessioned2024-02-15T06:45:45Z-
dc.date.available2024-02-15T06:45:45Z-
dc.date.created2024-02-22-
dc.date.issued2023-11-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198024-
dc.description.abstractPERLA is a global, double-blind, parallel phase II trial (NCT04581824) comparing efficacy and safety of anti-PD-1 antibodies dostarlimab and pembrolizumab, plus chemotherapy (DCT and PCT, respectively) as first-line treatment in patients with metastatic non-squamous NSCLC without known targetable genomic aberrations. Patients stratified by PD-L1 tumor proportion score and smoking status were randomized 1:1, receiving <= 35 cycles 500 mg dostarlimab or 200 mg pembrolizumab, <= 35 cycles 500 mg/m2 pemetrexed and <= 4 cycles cisplatin (75 mg/m2) or carboplatin (AUC 5 mg/ml/min) Q3W. Primary endpoint was overall response rate (ORR) (blinded independent central review). Secondary endpoints include progression-free survival (PFS) based on investigator assessment, overall survival (OS) and safety. Exploratory endpoints include ORR by PD-L1 subgroup and duration of response. PERLA met its pre-specified endpoint. ORR (n/N; 95% CI) is 45% (55/121; 36.4-54.8) for DCT and 39% (48/122; 30.6-48.6) for PCT (data cut-off: 07 July 23), numerically favoring dostarlimab in PD-L1-positive subgroups. Median PFS (months [95% CI]) is 8.8 (6.7-10.4) for DCT and 6.7 (4.9-7.1) for PCT (HR 0.70 [95% CI: 0.50-0.98]; data cut-off: 04 August 22). Median OS (months [95% CI]) is 19.4 (14.5-NR) for DCT and 15.9 (11.6-19.3) for PCT (HR 0.75 [95% CI: 0.53-1.05]) (data cut-off: 07 July 23). Safety profiles are similar between groups. In this study, DCT shows similar efficacy to PCT and demonstrates clinical efficacy as first-line treatment for patients with metastatic non-squamous NSCLC. Several PD-(L)1 inhibitors have been approved or are in development for the treatment of NSCLC, showing promising efficacy and tolerable safety profiles. Here, the authors present a randomized phase II clinical trial comparing two different anti-PD-1 antibodies, dostarlimab and pembrolizumab, both combined with chemotherapy as first-line treatment in patients with metastatic NSCLC.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Pub. Group-
dc.relation.isPartOfNATURE COMMUNICATIONS-
dc.relation.isPartOfNATURE COMMUNICATIONS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleDostarlimab or pembrolizumab plus chemotherapy in previously untreated metastatic non-squamous non-small cell lung cancer: the randomized PERLA phase II trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorLim, Sun Min-
dc.contributor.googleauthorPeters, Solange-
dc.contributor.googleauthorGranados, Ana Laura Ortega-
dc.contributor.googleauthorPinto, Gustavo dix Junqueira-
dc.contributor.googleauthorFuentes, Christian Sebastian-
dc.contributor.googleauthorLo Russo, Giuseppe-
dc.contributor.googleauthorSchenker, Michael-
dc.contributor.googleauthorAhn, Jin Seok-
dc.contributor.googleauthorReck, Martin-
dc.contributor.googleauthorSzijgyarto, Zsolt-
dc.contributor.googleauthorHuseinovic, Neda-
dc.contributor.googleauthorZografos, Eleftherios-
dc.contributor.googleauthorBuss, Elena-
dc.contributor.googleauthorStjepanovic, Neda-
dc.contributor.googleauthorODonnell, Sean-
dc.contributor.googleauthorde Marinis, Filippo-
dc.identifier.doi10.1038/s41467-023-42900-4-
dc.relation.journalcodeJ02293-
dc.identifier.eissn2041-1723-
dc.identifier.pmid37951954-
dc.contributor.alternativeNameLim, Sun Min-
dc.contributor.affiliatedAuthorLim, Sun Min-
dc.identifier.scopusid2-s2.0-85176577090-
dc.identifier.wosid001103534100004-
dc.citation.volume14-
dc.citation.number1-
dc.identifier.bibliographicCitationNATURE COMMUNICATIONS, Vol.14(1), 2023-11-
dc.identifier.rimsid82268-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.identifier.articleno7301-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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