Publication:
A Randomized, Placebo-Controlled Trial of Pembrolizumab Plus Chemotherapy in Patients With Metastatic Squamous NSCLC: Protocol-Specified Final Analysis of KEYNOTE-407.

dc.contributor.authorPaz-Ares, Luis
dc.contributor.authorVicente, David
dc.contributor.authorTafreshi, Ali
dc.contributor.authorRobinson, Andrew
dc.contributor.authorSoto Parra, Hector
dc.contributor.authorMazières, Julien
dc.contributor.authorHermes, Barbara
dc.contributor.authorCicin, Irfan
dc.contributor.authorMedgyasszay, Balazs
dc.contributor.authorRodríguez-Cid, Jerónimo
dc.contributor.authorOkamoto, Isamu
dc.contributor.authorLee, SungSook
dc.contributor.authorRamlau, Rodryg
dc.contributor.authorVladimirov, Vladimir
dc.contributor.authorCheng, Ying
dc.contributor.authorDeng, Xuan
dc.contributor.authorZhang, Ying
dc.contributor.authorBas, Tuba
dc.contributor.authorPiperdi, Bilal
dc.contributor.authorHalmos, Balazs
dc.date.accessioned2023-02-09T09:36:13Z
dc.date.available2023-02-09T09:36:13Z
dc.date.issued2020-06-26
dc.description.abstractIn the randomized KEYNOTE-407 study (ClinicalTrials.gov, NCT02775435), pembrolizumab plus carboplatin and paclitaxel/nab-paclitaxel (chemotherapy) significantly improved overall survival (OS) and progression-free survival (PFS) compared with placebo plus chemotherapy in patients with previously untreated metastatic squamous NSCLC. We report updated efficacy outcomes from the protocol-specified final analysis and, for the first time, progression on next line of treatment. Eligible patients were randomized to chemotherapy plus either pembrolizumab (n = 278) or placebo (n = 281). After positive results from the second interim analysis, patients still receiving placebo could cross over to pembrolizumab monotherapy at the time of confirmed progressive disease. The primary end points were OS and PFS. PFS-2 (time from randomization to progression on next-line treatment/death, whichever occurred first) was an exploratory end point. After median (range) follow-up of 14.3 (0.1-31.3) months, pembrolizumab plus chemotherapy continued to exhibit a clinically meaningful improvement over placebo plus chemotherapy in OS (median, 17.1 mo [95% confidence interval (CI): 14.4‒19.9] versus 11.6 mo [95% CI: 10.1‒13.7]; hazard ratio [HR], 0.71 [95% CI: 0.58‒0.88]) and PFS (median, 8.0 mo [95% CI: 6.3‒8.4] versus 5.1 mo [95% CI: 4.3‒6.0]; HR, 0.57 [95% CI: 0.47‒0.69]). PFS-2 was longer for patients randomized to first-line pembrolizumab plus chemotherapy (HR, 0.59 [95% CI: 0.49‒0.72]). Grade 3 to 5 adverse events occurred in 74.1% and 69.6% of patients receiving pembrolizumab plus chemotherapy and placebo plus chemotherapy, respectively. Pembrolizumab plus chemotherapy continued to exhibit substantially improved OS and PFS in patients with metastatic squamous NSCLC. The PFS-2 outcomes support pembrolizumab plus chemotherapy as a standard first-line treatment in patients with metastatic squamous NSCLC.
dc.identifier.doi10.1016/j.jtho.2020.06.015
dc.identifier.essn1556-1380
dc.identifier.pmid32599071
dc.identifier.unpaywallURLhttp://www.jto.org/article/S1556086420305001/pdf
dc.identifier.urihttp://hdl.handle.net/10668/15844
dc.issue.number10
dc.journal.titleJournal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
dc.journal.titleabbreviationJ Thorac Oncol
dc.language.isoen
dc.organizationHospital Universitario Virgen Macarena
dc.page.number1657-1669
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subjectChemotherapy
dc.subjectPD-L1
dc.subjectPembrolizumab
dc.subjectSquamous non–small-cell lung cancer
dc.subject.meshAntibodies, Monoclonal, Humanized
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshCarcinoma, Squamous Cell
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.titleA Randomized, Placebo-Controlled Trial of Pembrolizumab Plus Chemotherapy in Patients With Metastatic Squamous NSCLC: Protocol-Specified Final Analysis of KEYNOTE-407.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number15
dspace.entity.typePublication

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