Pembrolizumab plus chemotherapy for squamous non-small-cell lung cancer

dc.contributor.authorPaz-Ares, L.
dc.contributor.authorLuft, A.
dc.contributor.authorVicente, D.
dc.contributor.authorTafreshi, A.
dc.contributor.authorGümüş, M.
dc.contributor.authorMazières, J.
dc.contributor.authorHermes, B.
dc.date.accessioned2025-05-10T15:24:02Z
dc.date.issued2018
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBACKGROUND Standard first-line therapy for metastatic, squamous non-small-cell lung cancer (NSCLC) is platinum-based chemotherapy or pembrolizumab (for patients with programmed death ligand 1 [PD-L1] expression on ?50% of tumor cells). More recently, pembrolizumab plus chemotherapy was shown to significantly prolong overall survival among patients with nonsquamous NSCLC. METHODS In this double-blind, phase 3 trial, we randomly assigned, in a 1:1 ratio, 559 patients with untreated metastatic, squamous NSCLC to receive 200 mg of pembrolizumab or saline placebo for up to 35 cycles; all the patients also received carboplatin and either paclitaxel or nanoparticle albumin-bound [nab]-paclitaxel for the first 4 cycles. Primary end points were overall survival and progression-free survival. RESULTS After a median follow-up of 7.8 months, the median overall survival was 15.9 months (95% confidence interval [CI], 13.2 to not reached) in the pembrolizumab-combination group and 11.3 months (95% CI, 9.5 to 14.8) in the placebo-combination group (hazard ratio for death, 0.64; 95% CI, 0.49 to 0.85; P<0.001). The overall survival benefit was consistent regardless of the level of PD-L1 expression. The median progression-free survival was 6.4 months (95% CI, 6.2 to 8.3) in the pembrolizumab-combination group and 4.8 months (95% CI, 4.3 to 5.7) in the placebo-combination group (hazard ratio for disease progression or death, 0.56; 95% CI, 0.45 to 0.70; P<0.001). Adverse events of grade 3 or higher occurred in 69.8% of the patients in the pembrolizumab-combination group and in 68.2% of the patients in the placebo-combination group. Discontinuation of treatment because of adverse events was more frequent in the pembrolizumab-combination group than in the placebo-combination group (13.3% vs. 6.4%). CONCLUSIONS In patients with previously untreated metastatic, squamous NSCLC, the addition of pembrolizumab to chemotherapy with carboplatin plus paclitaxel or nab-paclitaxel resulted in significantly longer overall survival and progression-free survival than chemotherapy alone. Copyright © 2018 Massachusetts Medical Society.
dc.identifier.doi10.1056/NEJMoa1810865
dc.identifier.endpage2051
dc.identifier.issn0028-4793
dc.identifier.issue21
dc.identifier.pmid30280635
dc.identifier.scopus2-s2.0-85054684704
dc.identifier.scopusqualityQ1
dc.identifier.startpage2040
dc.identifier.urihttps://doi.org/10.1056/NEJMoa1810865
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6610
dc.identifier.volume379
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMassachussetts Medical Society
dc.relation.ispartofNew England Journal of Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_Scopus_20250302
dc.subjectAdult; Aged; Aged, 80 and over; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Protocols; Carboplatin; Carcinoma, Non-Small-Cell Lung; Double-Blind Method; Female; Humans; Intention to Treat Analysis; Lung Neoplasms; Male; Middle Aged; Paclitaxel; Programmed Cell Death 1 Receptor; Progression-Free Survival; Survival Analysis; atezolizumab; carboplatin; ipilimumab; paclitaxel; pembrolizumab; placebo; programmed death 1 receptor; sodium chloride; antineoplastic agent; carboplatin; monoclonal antibody; paclitaxel; pembrolizumab; programmed death 1 receptor; add on therapy; adult; aged; alopecia; anemia; arthralgia; Article; asthenia; autoimmune hepatitis; cancer chemotherapy; cancer combination chemotherapy; colitis; constipation; controlled study; coughing; decreased appetite; diarrhea; double blind procedure; drug efficacy; drug withdrawal; dyspnea; fatigue; female; follow up; hepatitis; human; hyperthyroidism; hypophysitis; hypothyroidism; lung metastasis; major clinical study; male; monotherapy; multiple cycle treatment; nausea; nephritis; neutropenia; overall survival; peripheral neuropathy; phase 3 clinical trial; pneumonia; priority journal; progression free survival; protein expression; randomized controlled trial; skin manifestation; squamous cell lung carcinoma; thrombocytopenia; thyroiditis; very elderly; vomiting; antagonists and inhibitors; clinical trial; intention to treat analysis; lung tumor; middle aged; mortality; multicenter study; non small cell lung cancer; secondary; survival analysis
dc.titlePembrolizumab plus chemotherapy for squamous non-small-cell lung cancer
dc.typeArticle

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