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Second-line nivolumab in relapsed small-cell lung cancer: CheckMate 331☆.
Spigel, D R; Vicente, D; Ciuleanu, T E; Gettinger, S; Peters, S; Horn, L; Audigier-Valette, C; Pardo Aranda, N; Juan-Vidal, O; Cheng, Y; Zhang, H; Shi, M; Luft, A; Wolf, J; Antonia, S; Nakagawa, K; Fairchild, J; Baudelet, C; Pandya, D; Doshi, P; Chang, H; Reck, M.
Afiliação
  • Spigel DR; Oncology Department, Sarah Cannon Research Institute/Tennessee Oncology, PLLC, Nashville, USA. Electronic address: David.spigel@sarahcannon.com.
  • Vicente D; Department of Medical Oncology, Hosp Univ Virgen Macarena, Seville, Spain.
  • Ciuleanu TE; Medical Oncology, Prof. Dr. Ion Chiricuta Institute of Oncology and UMF Iuliu Hatieganu, Cluj-Napoca, Romania.
  • Gettinger S; Medical Oncology, Yale Cancer Center, New Haven, USA.
  • Peters S; Oncology Department, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
  • Horn L; Department of Medicine, Vanderbilt-Ingram Cancer Center, Nashville, USA.
  • Audigier-Valette C; Pulmonology Department, Hôpital Sainte Musse, Toulon, France.
  • Pardo Aranda N; Thoracic Unit, Medical Oncology Department, Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology (VHIO), Barcelona.
  • Juan-Vidal O; Department of Medical Oncology, Hospital Universitario La Fe, Valencia, Spain.
  • Cheng Y; Department of Thoracic Oncology, Jilin Cancer Hospital, Changchun, Jilin, China.
  • Zhang H; Department of Oncology, Tangdu Hospital, Xi'an, Shaanxi, China.
  • Shi M; Department of Medical Oncology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
  • Luft A; Department of Thoracic Surgery, Leningrad Regional Clinical Hospital, St. Petersburg, Russian Federation.
  • Wolf J; Clinic I for Internal Medicine, Center for Integrated Oncology, University Hospital of Cologne, Cologne, Germany.
  • Antonia S; Department of Thoracic Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, USA.
  • Nakagawa K; Department of Medical Oncology, Kindai University Hospital, Osaka, Japan.
  • Fairchild J; Clinical Development, Bristol Myers Squibb, Princeton, USA.
  • Baudelet C; Global Drug Development, Biometrics & Data Sciences, Bristol Myers Squibb, Princeton, USA.
  • Pandya D; Translational Pathology, Bristol Myers Squibb, Princeton, USA.
  • Doshi P; Translational Medicine, Bristol Myers Squibb, Princeton, USA.
  • Chang H; Translational Bioinformatics, Bristol Myers Squibb, Princeton, USA.
  • Reck M; Thoracic Oncology, LungenClinic Grosshansdorf, Airway Research Center North, German Center of Lung Research, Grosshansdorf, Germany.
Ann Oncol ; 32(5): 631-641, 2021 05.
Article em En | MEDLINE | ID: mdl-33539946
ABSTRACT

BACKGROUND:

Patients with relapsed small-cell lung cancer (SCLC) have few treatment options and dismal survival. Phase I/II data show activity of nivolumab in previously treated SCLC. PATIENTS AND

METHODS:

CheckMate 331 is a randomized, open-label, phase III trial of nivolumab versus standard chemotherapy in relapsed SCLC. Patients with relapse after first-line, platinum-based chemotherapy were randomized 1 1 to nivolumab 240 mg every 2 weeks or chemotherapy (topotecan or amrubicin) until progression or unacceptable toxicity. Primary endpoint was overall survival (OS).

RESULTS:

Overall, 284 patients were randomized to nivolumab and 285 to chemotherapy. Minimum follow-up was 15.8 months. No significant improvement in OS was seen with nivolumab versus chemotherapy [median OS, 7.5 versus 8.4 months; hazard ratio (HR), 0.86; 95% confidence interval (CI), 0.72-1.04; P = 0.11]. A survival benefit with nivolumab was suggested in patients with baseline lactate dehydrogenase ≤ upper limit of normal and in those without baseline liver metastases. OS (nivolumab versus chemotherapy) was similar in patients with programmed death-ligand 1 combined positive score ≥1% versus <1%. Median progression-free survival was 1.4 versus 3.8 months (HR, 1.41; 95% CI, 1.18-1.69). Objective response rate was 13.7% versus 16.5% (odds ratio, 0.80; 95% CI, 0.50-1.27); median duration of response was 8.3 versus 4.5 months. Rates of grade 3 or 4 treatment-related adverse events were 13.8% versus 73.2%.

CONCLUSION:

Nivolumab did not improve survival versus chemotherapy in relapsed SCLC. No new safety signals were seen. In exploratory analyses, select baseline characteristics were associated with improved OS for nivolumab.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Carcinoma de Pequenas Células do Pulmão / Neoplasias Pulmonares Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Ann Oncol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Carcinoma de Pequenas Células do Pulmão / Neoplasias Pulmonares Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Ann Oncol Ano de publicação: 2021 Tipo de documento: Article