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Nivolumab for Recurrent Squamous-Cell Carcinoma of the Head and Neck
5.030
Zitationen
23
Autoren
2016
Jahr
Abstract
BACKGROUND: Patients with recurrent or metastatic squamous-cell carcinoma of the head and neck after platinum chemotherapy have a very poor prognosis and limited therapeutic options. Nivolumab, an anti-programmed death 1 (PD-1) monoclonal antibody, was assessed as treatment for this condition. METHODS: In this randomized, open-label, phase 3 trial, we assigned, in a 2:1 ratio, 361 patients with recurrent squamous-cell carcinoma of the head and neck whose disease had progressed within 6 months after platinum-based chemotherapy to receive nivolumab (at a dose of 3 mg per kilogram of body weight) every 2 weeks or standard, single-agent systemic therapy (methotrexate, docetaxel, or cetuximab). The primary end point was overall survival. Additional end points included progression-free survival, rate of objective response, safety, and patient-reported quality of life. RESULTS: The median overall survival was 7.5 months (95% confidence interval [CI], 5.5 to 9.1) in the nivolumab group versus 5.1 months (95% CI, 4.0 to 6.0) in the group that received standard therapy. Overall survival was significantly longer with nivolumab than with standard therapy (hazard ratio for death, 0.70; 97.73% CI, 0.51 to 0.96; P=0.01), and the estimates of the 1-year survival rate were approximately 19 percentage points higher with nivolumab than with standard therapy (36.0% vs. 16.6%). The median progression-free survival was 2.0 months (95% CI, 1.9 to 2.1) with nivolumab versus 2.3 months (95% CI, 1.9 to 3.1) with standard therapy (hazard ratio for disease progression or death, 0.89; 95% CI, 0.70 to 1.13; P=0.32). The rate of progression-free survival at 6 months was 19.7% with nivolumab versus 9.9% with standard therapy. The response rate was 13.3% in the nivolumab group versus 5.8% in the standard-therapy group. Treatment-related adverse events of grade 3 or 4 occurred in 13.1% of the patients in the nivolumab group versus 35.1% of those in the standard-therapy group. Physical, role, and social functioning was stable in the nivolumab group, whereas it was meaningfully worse in the standard-therapy group. CONCLUSIONS: Among patients with platinum-refractory, recurrent squamous-cell carcinoma of the head and neck, treatment with nivolumab resulted in longer overall survival than treatment with standard, single-agent therapy. (Funded by Bristol-Myers Squibb; CheckMate 141 ClinicalTrials.gov number, NCT02105636 .).
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Autoren
- Robert L. Ferris
- George R. Blumenschein
- Jérôme Fayette
- J. Guigay
- A. Dimitrios Colevas
- Lisa Licitra
- Kevin J. Harrington
- Stefan Kasper
- Everett E. Vokes
- Caroline Even
- Francis P. Worden
- Nabil F. Saba
- Lara Carmen Iglesias Docampo
- Robert I. Haddad
- Tamara Rordorf
- Naomi Kiyota
- Makoto Tahara
- Manish Monga
- Mark Lynch
- William J. Geese
- Justin Kopit
- James W. Shaw
- Maura L. Gillison
Institutionen
- University of Pittsburgh Medical Center(US)
- Institut Gustave Roussy(FR)
- Cancer Institute (WIA)(IN)
- The University of Texas MD Anderson Cancer Center(US)
- Centre Léon Bérard(FR)
- Centre Antoine Lacassagne(FR)
- Cancer Prevention Institute of California(US)
- Stanford Cancer Institute
- Fondazione IRCCS Istituto Nazionale dei Tumori(IT)
- National Institute for Health Research(GB)
- NIHR Biomedical Research Centre at The Royal Marsden and the ICR
- Essen University Hospital(DE)
- University of Chicago(US)
- University of Michigan–Ann Arbor(US)
- Emory University(US)
- Hospital Universitario 12 De Octubre(ES)
- Dana-Farber Cancer Institute(US)
- University Hospital of Zurich(CH)
- Kobe University Hospital(JP)
- National Cancer Center Hospital East(JP)
- Bristol-Myers Squibb (United States)(US)
- The Ohio State University(US)