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A Brief Report of Durvalumab With or Without Tremelimumab in Combination With Chemotherapy as First-Line Therapy for Metastatic Non-Small-Cell Lung Cancer: Outcomes by Tumor PD-L1 Expression in the Phase 3 POSEIDON Study

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dc.contributor.authorGaron, Edward B.-
dc.contributor.authorCho, Byoung Chul-
dc.contributor.authorLuft, Alexander-
dc.contributor.authorAlatorre-Alexander, Jorge-
dc.contributor.authorGeater, Sarayut Lucien-
dc.contributor.authorTrukhin, Dmytro-
dc.contributor.authorKim, Sang -We-
dc.contributor.authorUrsol, Grygorii-
dc.contributor.authorHussein, Maen-
dc.contributor.authorLim, Farah Louise-
dc.contributor.authorYang, Cheng-Ta-
dc.contributor.authorAraujo, Luiz Henrique-
dc.contributor.authorSaito, Haruhiro-
dc.contributor.authorReinmuth, Niels-
dc.contributor.authorKohlmann, Milena-
dc.contributor.authorLowery, Caitlin-
dc.contributor.authorMann, Helen-
dc.contributor.authorPeters, Solange-
dc.contributor.authorMok, Tony S.-
dc.contributor.authorJohnson, Melissa L.-
dc.date.accessioned2024-10-04T02:44:55Z-
dc.date.available2024-10-04T02:44:55Z-
dc.date.created2025-02-19-
dc.date.issued2024-05-
dc.identifier.issn1525-7304-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/200583-
dc.description.abstract• In the phase 3 POSEIDON study, patients with EGFR/ALK wild-type metastatic NSCLC (mNSCLC) were randomized (1:1:1) to first-line tremelimumab plus durvalumab and platinum-based chemotherapy (T + D + CT), durvalumab plus chemotherapy (D + CT), or chemotherapy alone (CT), with stratification by programmed cell death ligand-1 (PD-L1) tumor cell (TC) expression level (≥ 50% vs. < 50%), disease stage, and histology. • In alpha-controlled analyses in the ITT population, T + D + CT significantly improved overall survival (OS) and progression-free survival (PFS) versus CT, leading to approval for this regimen. PFS was also significantly improved with D + CT versus CT; a trend for improved OS did not reach statistical significance. • Patients with PD-L1-low or -negative tumors may show primary resistance to anti-PD-(L)1 therapy, with real-world data suggesting that treatment benefits observed in trials do not always translate into optimal outcomes in clinical practice. • Here we report outcomes from POSEIDON from post-hoc exploratory analyses in subgroups with PD-L1 TC ≥ 1% versus < 1%. • Among 1012/1013 randomized patients with known PD-L1 status, 644 (63.6%) versus 368 (36.4%) had PD-L1 TC ≥ 1% versus < 1%. • Both T + D + CT and D + CT appeared to show OS/PFS benefit versus CT in patients with PD-L1 TC ≥ 1%. • Consistent with the role of cytotoxic T-lymphocyte-associated antigen 4 and PD-L1 in the immune response, the addition of tremelimumab to first-line durvalumab and chemotherapy also conferred clinical benefit to patients with PD-L1 TC < 1% mNSCLC. • This exploratory subgroup analysis of POSEIDON supports T + D + CT as a first-line treatment option for patients with mNSCLC irrespective of PD-L1 expression, including the harder-to-treat subgroup with PD-L1 TC < 1%. © 2024 The Authors-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.language영어-
dc.publisherCIG MEDIA GROUP, LP-
dc.relation.isPartOfCLINICAL LUNG CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleA Brief Report of Durvalumab With or Without Tremelimumab in Combination With Chemotherapy as First-Line Therapy for Metastatic Non-Small-Cell Lung Cancer: Outcomes by Tumor PD-L1 Expression in the Phase 3 POSEIDON Study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorGaron, Edward B.-
dc.contributor.googleauthorCho, Byoung Chul-
dc.contributor.googleauthorLuft, Alexander-
dc.contributor.googleauthorAlatorre-Alexander, Jorge-
dc.contributor.googleauthorGeater, Sarayut Lucien-
dc.contributor.googleauthorTrukhin, Dmytro-
dc.contributor.googleauthorKim, Sang -We-
dc.contributor.googleauthorUrsol, Grygorii-
dc.contributor.googleauthorHussein, Maen-
dc.contributor.googleauthorLim, Farah Louise-
dc.contributor.googleauthorYang, Cheng-Ta-
dc.contributor.googleauthorAraujo, Luiz Henrique-
dc.contributor.googleauthorSaito, Haruhiro-
dc.contributor.googleauthorReinmuth, Niels-
dc.contributor.googleauthorKohlmann, Milena-
dc.contributor.googleauthorLowery, Caitlin-
dc.contributor.googleauthorMann, Helen-
dc.contributor.googleauthorPeters, Solange-
dc.contributor.googleauthorMok, Tony S.-
dc.contributor.googleauthorJohnson, Melissa L.-
dc.identifier.doi10.1016/j.cllc.2024.03.003-
dc.identifier.eissn1938-0690-
dc.identifier.pmid38584069-
dc.subject.keywordImmunotherapy-
dc.subject.keywordImmune checkpoint inhibitor-
dc.subject.keywordProgrammed cell death ligand-1-
dc.subject.keywordCytotoxic T-lymphocyte-associated antigen 4-
dc.subject.keywordClinical trial-
dc.contributor.alternativeNameCho, Byoung Chul-
dc.contributor.affiliatedAuthorCho, Byoung Chul-
dc.identifier.scopusid2-s2.0-85189662618-
dc.identifier.wosid001244527100001-
dc.citation.volume25-
dc.citation.number3-
dc.citation.startPage266-
dc.citation.endPage273.e5-
dc.identifier.bibliographicCitationCLINICAL LUNG CANCER, Vol.25(3) : 266-273.e5, 2024-05-
dc.identifier.rimsid84904-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorImmunotherapy-
dc.subject.keywordAuthorImmune checkpoint inhibitor-
dc.subject.keywordAuthorProgrammed cell death ligand-1-
dc.subject.keywordAuthorCytotoxic T-lymphocyte-associated antigen 4-
dc.subject.keywordAuthorClinical trial-
dc.subject.keywordPlusREAL-WORLD-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
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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