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- Publisher Website: 10.1056/NEJMoa1801005
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- PMID: 29658856
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Article: Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer
Title | Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer |
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Authors | Gandhi, L.Rodríguez-Abreu, D.Gadgeel, S.Esteban, E.Felip, E.De Angelis, F.Domine, M.Clingan, P.Hochmair, M. J.Powell, S. F.Cheng, S. Y.S.Bischoff, H. G.Peled, N.Grossi, F.Jennens, R. R.Reck, M.Hui, R.Garon, E. B.Boyer, M.Rubio-Viqueira, B.Novello, S.Kurata, T.Gray, J. E.Vida, J.Wei, Z.Yang, J.Raftopoulos, H.Pietanza, M. C.Garassino, M. C. |
Issue Date | 2018 |
Citation | New England Journal of Medicine, 2018, v. 378, n. 22, p. 2078-2092 How to Cite? |
Abstract | BACKGROUND First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial. METHODS In this double-blind, phase 3 trial, we randomly assigned (in a 2:1 ratio) 616 patients with metastatic nonsquamous NSCLC without sensitizing EGFR or ALK mutations who had received no previous treatment for metastatic disease to receive pemetrexed and a platinum-based drug plus either 200 mg of pembrolizumab or placebo every 3 weeks for 4 cycles, followed by pembrolizumab or placebo for up to a total of 35 cycles plus pemetrexed maintenance therapy. Crossover to pembrolizumab monotherapy was permitted among the patients in the placebo-combination group who had verified disease progression. The primary end points were overall survival and progression-free survival, as assessed by blinded, independent central radiologic review. RESULTS After a median follow-up of 10.5 months, the estimated rate of overall survival at 12 months was 69.2% (95% confidence interval [CI], 64.1 to 73.8) in the pembrolizumab- combination group versus 49.4% (95% CI, 42.1 to 56.2) in the placebocombination group (hazard ratio for death, 0.49; 95% CI, 0.38 to 0.64; P<0.001). Improvement in overall survival was seen across all PD-L1 categories that were evaluated. Median progression-free survival was 8.8 months (95% CI, 7.6 to 9.2) in the pembrolizumab-combination group and 4.9 months (95% CI, 4.7 to 5.5) in the placebo-combination group (hazard ratio for disease progression or death, 0.52; 95% CI, 0.43 to 0.64; P<0.001). Adverse events of grade 3 or higher occurred in 67.2% of the patients in the pembrolizumab-combination group and in 65.8% of those in the placebo-combination group. CONCLUSIONS In patients with previously untreated metastatic nonsquamous NSCLC without EGFR or ALK mutations, the addition of pembrolizumab to standard chemotherapy of pemetrexed and a platinum-based drug resulted in significantly longer overall survival and progression-free survival than chemotherapy alone. |
Persistent Identifier | http://hdl.handle.net/10722/326476 |
ISSN | 2023 Impact Factor: 96.2 2023 SCImago Journal Rankings: 20.544 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Gandhi, L. | - |
dc.contributor.author | Rodríguez-Abreu, D. | - |
dc.contributor.author | Gadgeel, S. | - |
dc.contributor.author | Esteban, E. | - |
dc.contributor.author | Felip, E. | - |
dc.contributor.author | De Angelis, F. | - |
dc.contributor.author | Domine, M. | - |
dc.contributor.author | Clingan, P. | - |
dc.contributor.author | Hochmair, M. J. | - |
dc.contributor.author | Powell, S. F. | - |
dc.contributor.author | Cheng, S. Y.S. | - |
dc.contributor.author | Bischoff, H. G. | - |
dc.contributor.author | Peled, N. | - |
dc.contributor.author | Grossi, F. | - |
dc.contributor.author | Jennens, R. R. | - |
dc.contributor.author | Reck, M. | - |
dc.contributor.author | Hui, R. | - |
dc.contributor.author | Garon, E. B. | - |
dc.contributor.author | Boyer, M. | - |
dc.contributor.author | Rubio-Viqueira, B. | - |
dc.contributor.author | Novello, S. | - |
dc.contributor.author | Kurata, T. | - |
dc.contributor.author | Gray, J. E. | - |
dc.contributor.author | Vida, J. | - |
dc.contributor.author | Wei, Z. | - |
dc.contributor.author | Yang, J. | - |
dc.contributor.author | Raftopoulos, H. | - |
dc.contributor.author | Pietanza, M. C. | - |
dc.contributor.author | Garassino, M. C. | - |
dc.date.accessioned | 2023-03-10T02:19:33Z | - |
dc.date.available | 2023-03-10T02:19:33Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | New England Journal of Medicine, 2018, v. 378, n. 22, p. 2078-2092 | - |
dc.identifier.issn | 0028-4793 | - |
dc.identifier.uri | http://hdl.handle.net/10722/326476 | - |
dc.description.abstract | BACKGROUND First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial. METHODS In this double-blind, phase 3 trial, we randomly assigned (in a 2:1 ratio) 616 patients with metastatic nonsquamous NSCLC without sensitizing EGFR or ALK mutations who had received no previous treatment for metastatic disease to receive pemetrexed and a platinum-based drug plus either 200 mg of pembrolizumab or placebo every 3 weeks for 4 cycles, followed by pembrolizumab or placebo for up to a total of 35 cycles plus pemetrexed maintenance therapy. Crossover to pembrolizumab monotherapy was permitted among the patients in the placebo-combination group who had verified disease progression. The primary end points were overall survival and progression-free survival, as assessed by blinded, independent central radiologic review. RESULTS After a median follow-up of 10.5 months, the estimated rate of overall survival at 12 months was 69.2% (95% confidence interval [CI], 64.1 to 73.8) in the pembrolizumab- combination group versus 49.4% (95% CI, 42.1 to 56.2) in the placebocombination group (hazard ratio for death, 0.49; 95% CI, 0.38 to 0.64; P<0.001). Improvement in overall survival was seen across all PD-L1 categories that were evaluated. Median progression-free survival was 8.8 months (95% CI, 7.6 to 9.2) in the pembrolizumab-combination group and 4.9 months (95% CI, 4.7 to 5.5) in the placebo-combination group (hazard ratio for disease progression or death, 0.52; 95% CI, 0.43 to 0.64; P<0.001). Adverse events of grade 3 or higher occurred in 67.2% of the patients in the pembrolizumab-combination group and in 65.8% of those in the placebo-combination group. CONCLUSIONS In patients with previously untreated metastatic nonsquamous NSCLC without EGFR or ALK mutations, the addition of pembrolizumab to standard chemotherapy of pemetrexed and a platinum-based drug resulted in significantly longer overall survival and progression-free survival than chemotherapy alone. | - |
dc.language | eng | - |
dc.relation.ispartof | New England Journal of Medicine | - |
dc.title | Pembrolizumab plus chemotherapy in metastatic non-small-cell lung cancer | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1056/NEJMoa1801005 | - |
dc.identifier.pmid | 29658856 | - |
dc.identifier.scopus | eid_2-s2.0-85047328215 | - |
dc.identifier.volume | 378 | - |
dc.identifier.issue | 22 | - |
dc.identifier.spage | 2078 | - |
dc.identifier.epage | 2092 | - |
dc.identifier.eissn | 1533-4406 | - |
dc.identifier.isi | WOS:000433428000006 | - |