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Five-Year Outcomes With Pembrolizumab Versus Chemotherapy for Metastatic Non-Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score ≥ 50.
Reck, Martin; Rodríguez-Abreu, Delvys; Robinson, Andrew G; Hui, Rina; Csoszi, Tibor; Fülöp, Andrea; Gottfried, Maya; Peled, Nir; Tafreshi, Ali; Cuffe, Sinead; O'Brien, Mary; Rao, Suman; Hotta, Katsuyuki; Leal, Ticiana A; Riess, Jonathan W; Jensen, Erin; Zhao, Bin; Pietanza, M Catherine; Brahmer, Julie R.
Afiliação
  • Reck M; Lung Clinic Grosshansdorf, Airway Research Center North (ARCN), member of the German Center for Lung Research (DZL), Grosshansdorf, Germany.
  • Rodríguez-Abreu D; Complejo Hospitalario Universitario Insular Materno-Infantil de Gran Canaria, Universidad de Las Palmas de Gran Canaria, Las Palmas, Spain.
  • Robinson AG; Cancer Centre of Southeastern Ontario at Kingston General Hospital, Kingston, ON, Canada.
  • Hui R; Westmead Hospital and the University of Sydney, Sydney, NSW, Australia.
  • Csoszi T; Jász-Nagykun-Szolnok County Hospital, Szolnok, Hungary.
  • Fülöp A; Országos Korányi Pulmonológiai Intézet, Budapest, Hungary.
  • Gottfried M; Meir Medical Center, Kfar-Saba, Israel.
  • Peled N; Soroka Cancer Center, Ben Gurion University, Beer Sheva, Israel.
  • Tafreshi A; Wollongong Private Hospital and University of Wollongong, Wollongong, NSW, Australia.
  • Cuffe S; St James's Hospital and Cancer Trials Ireland (formerly ICORG-All Ireland Cooperative Oncology Research Group), Dublin, Ireland.
  • O'Brien M; The Royal Marsden Hospital, Sutton, Surrey, UK.
  • Rao S; MedStar Franklin Square Hospital, Baltimore, MD.
  • Hotta K; Okayama University Hospital, Okayama, Japan.
  • Leal TA; Carbone Cancer Center, University of Wisconsin, Madison, WI.
  • Riess JW; UC Davis Comprehensive Cancer Center, Sacramento, CA.
  • Jensen E; Merck & Co, Inc, Kenilworth, NJ.
  • Zhao B; Merck & Co, Inc, Kenilworth, NJ.
  • Pietanza MC; Merck & Co, Inc, Kenilworth, NJ.
  • Brahmer JR; Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD.
J Clin Oncol ; 39(21): 2339-2349, 2021 07 20.
Article em En | MEDLINE | ID: mdl-33872070
ABSTRACT

PURPOSE:

We report the first 5-year follow-up of any first-line phase III immunotherapy trial for non-small-cell lung cancer (NSCLC). KEYNOTE-024 (ClinicalTrials.gov identifier NCT02142738) is an open-label, randomized controlled trial of pembrolizumab compared with platinum-based chemotherapy in patients with previously untreated NSCLC with a programmed death ligand-1 (PD-L1) tumor proportion score of at least 50% and no sensitizing EGFR or ALK alterations. Previous analyses showed pembrolizumab significantly improved progression-free survival and overall survival (OS).

METHODS:

Eligible patients were randomly assigned (11) to pembrolizumab (200 mg once every 3 weeks for up to 35 cycles) or platinum-based chemotherapy. Patients in the chemotherapy group with progressive disease could cross over to pembrolizumab. The primary end point was progression-free survival; OS was a secondary end point.

RESULTS:

Three hundred five patients were randomly assigned 154 to pembrolizumab and 151 to chemotherapy. Median (range) time from randomization to data cutoff (June 1, 2020) was 59.9 (55.1-68.4) months. Among patients initially assigned to chemotherapy, 99 received subsequent anti-PD-1 or PD-L1 therapy, representing a 66.0% effective crossover rate. Median OS was 26.3 months (95% CI, 18.3 to 40.4) for pembrolizumab and 13.4 months (9.4-18.3) for chemotherapy (hazard ratio, 0.62; 95% CI, 0.48 to 0.81). Kaplan-Meier estimates of the 5-year OS rate were 31.9% for the pembrolizumab group and 16.3% for the chemotherapy group. Thirty-nine patients received 35 cycles (ie, approximately 2 years) of pembrolizumab, 82.1% of whom were still alive at data cutoff (approximately 5 years). Toxicity did not increase with longer treatment exposure.

CONCLUSION:

Pembrolizumab provides a durable, clinically meaningful long-term OS benefit versus chemotherapy as first-line therapy for metastatic NSCLC with PD-L1 tumor proportion score of at least 50%.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Anticorpos Monoclonais Humanizados / Neoplasias Pulmonares Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Anticorpos Monoclonais Humanizados / Neoplasias Pulmonares Idioma: En Ano de publicação: 2021 Tipo de documento: Article