Publication: Nivolumab Versus Docetaxel in Previously Treated Patients With Advanced Non-Small-Cell Lung Cancer: Two-Year Outcomes From Two Randomized, Open-Label, Phase III Trials (CheckMate 017 and CheckMate 057).
dc.contributor.author | Horn, Leora | |
dc.contributor.author | Spigel, David R | |
dc.contributor.author | Vokes, Everett E | |
dc.contributor.author | Holgado, Esther | |
dc.contributor.author | Ready, Neal | |
dc.contributor.author | Steins, Martin | |
dc.contributor.author | Poddubskaya, Elena | |
dc.contributor.author | Borghaei, Hossein | |
dc.contributor.author | Felip, Enriqueta | |
dc.contributor.author | Paz-Ares, Luis | |
dc.contributor.author | Pluzanski, Adam | |
dc.contributor.author | Reckamp, Karen L | |
dc.contributor.author | Burgio, Marco A | |
dc.contributor.author | Kohlhäeufl, Martin | |
dc.contributor.author | Waterhouse, David | |
dc.contributor.author | Barlesi, Fabrice | |
dc.contributor.author | Antonia, Scott | |
dc.contributor.author | Arrieta, Oscar | |
dc.contributor.author | Fayette, Jérôme | |
dc.contributor.author | Crinò, Lucio | |
dc.contributor.author | Rizvi, Naiyer | |
dc.contributor.author | Reck, Martin | |
dc.contributor.author | Hellmann, Matthew D | |
dc.contributor.author | Geese, William J | |
dc.contributor.author | Li, Ang | |
dc.contributor.author | Blackwood-Chirchir, Anne | |
dc.contributor.author | Healey, Diane | |
dc.contributor.author | Brahmer, Julie | |
dc.contributor.author | Eberhardt, Wilfried E E | |
dc.date.accessioned | 2023-01-25T10:00:53Z | |
dc.date.available | 2023-01-25T10:00:53Z | |
dc.date.issued | 2017-10-12 | |
dc.description.abstract | Purpose Nivolumab, a programmed death-1 inhibitor, prolonged overall survival compared with docetaxel in two independent phase III studies in previously treated patients with advanced squamous (CheckMate 017; ClinicalTrials.gov identifier: NCT01642004) or nonsquamous (CheckMate 057; ClinicalTrials.gov identifier: NCT01673867) non-small-cell lung cancer (NSCLC). We report updated results, including a pooled analysis of the two studies. Methods Patients with stage IIIB/IV squamous (N = 272) or nonsquamous (N = 582) NSCLC and disease progression during or after prior platinum-based chemotherapy were randomly assigned 1:1 to nivolumab (3 mg/kg every 2 weeks) or docetaxel (75 mg/m2 every 3 weeks). Minimum follow-up for survival was 24.2 months. Results Two-year overall survival rates with nivolumab versus docetaxel were 23% (95% CI, 16% to 30%) versus 8% (95% CI, 4% to 13%) in squamous NSCLC and 29% (95% CI, 24% to 34%) versus 16% (95% CI, 12% to 20%) in nonsquamous NSCLC; relative reductions in the risk of death with nivolumab versus docetaxel remained similar to those reported in the primary analyses. Durable responses were observed with nivolumab; 10 (37%) of 27 confirmed responders with squamous NSCLC and 19 (34%) of 56 with nonsquamous NSCLC had ongoing responses after 2 years' minimum follow-up. No patient in either docetaxel group had an ongoing response. In the pooled analysis, the relative reduction in the risk of death with nivolumab versus docetaxel was 28% (hazard ratio, 0.72; 95% CI, 0.62 to 0.84), and rates of treatment-related adverse events were lower with nivolumab than with docetaxel (any grade, 68% v 88%; grade 3 to 4, 10% v 55%). Conclusion Nivolumab provides long-term clinical benefit and a favorable tolerability profile compared with docetaxel in previously treated patients with advanced NSCLC. | |
dc.identifier.doi | 10.1200/JCO.2017.74.3062 | |
dc.identifier.essn | 1527-7755 | |
dc.identifier.pmc | PMC6075826 | |
dc.identifier.pmid | 29023213 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6075826/pdf | |
dc.identifier.unpaywallURL | https://europepmc.org/articles/pmc6075826?pdf=render | |
dc.identifier.uri | http://hdl.handle.net/10668/11674 | |
dc.issue.number | 35 | |
dc.journal.title | Journal of clinical oncology : official journal of the American Society of Clinical Oncology | |
dc.journal.titleabbreviation | J Clin Oncol | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 3924-3933 | |
dc.pubmedtype | Clinical Trial, Phase III | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Multicenter Study | |
dc.pubmedtype | Randomized Controlled Trial | |
dc.rights.accessRights | open access | |
dc.subject.mesh | Antibodies, Monoclonal | |
dc.subject.mesh | Antineoplastic Agents | |
dc.subject.mesh | Carcinoma, Non-Small-Cell Lung | |
dc.subject.mesh | Docetaxel | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Kaplan-Meier Estimate | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Nivolumab | |
dc.subject.mesh | Survival Rate | |
dc.subject.mesh | Taxoids | |
dc.subject.mesh | Treatment Outcome | |
dc.title | Nivolumab Versus Docetaxel in Previously Treated Patients With Advanced Non-Small-Cell Lung Cancer: Two-Year Outcomes From Two Randomized, Open-Label, Phase III Trials (CheckMate 017 and CheckMate 057). | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 35 | |
dspace.entity.type | Publication |