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Five-year survival outcomes for patients with advanced melanoma treated with pembrolizumab in KEYNOTE-001.
Hamid, O; Robert, C; Daud, A; Hodi, F S; Hwu, W J; Kefford, R; Wolchok, J D; Hersey, P; Joseph, R; Weber, J S; Dronca, R; Mitchell, T C; Patnaik, A; Zarour, H M; Joshua, A M; Zhao, Q; Jensen, E; Ahsan, S; Ibrahim, N; Ribas, A.
Afiliación
  • Hamid O; Medical Oncology, The Angeles Clinic and Research Institute, Los Angeles, USA. Electronic address: ohamid@theangelesclinic.org.
  • Robert C; Department of Dermatology, Gustave Roussy, Villejuif; Department of Medicine, University of Paris-Sud, Paris, France.
  • Daud A; Department of Medicine, University of California, San Francisco, San Francisco.
  • Hodi FS; Medical Oncology, Dana-Farber Cancer Institute, Boston.
  • Hwu WJ; Department of Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA.
  • Kefford R; Medical Oncology, Westmead Hospital, Westmead; Medical Oncology, Melanoma Institute Australia, Sydney; Medical Oncology, Macquarie University, Macquarie Park; Medical Oncology, University of Sydney, Sydney, Australia.
  • Wolchok JD; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, USA.
  • Hersey P; Medical Oncology, University of Sydney, Sydney, Australia; Department of Medicine, Centenary Institute, Sydney, Australia.
  • Joseph R; Medical Oncology, Mayo Clinic Cancer Center-Florida, Jacksonville.
  • Weber JS; Department of Medicine, Perlmutter Cancer Center, NYU Langone Health, New York.
  • Dronca R; Medical Oncology, Mayo Clinic Cancer Center-Florida, Jacksonville.
  • Mitchell TC; Division of Hematology Oncology, Abramson Cancer Center, Perelman Center for Advanced Medicine, University of Pennsylvania, Philadelphia.
  • Patnaik A; Medical Oncology, South Texas Accelerated Research Therapeutics, San Antonio.
  • Zarour HM; Department of Immunology, University of Pittsburgh Cancer Institute, Pittsburgh, USA.
  • Joshua AM; Medical Oncology, Melanoma Institute Australia, Sydney; Medical Oncology, University of Sydney, Sydney, Australia; Kinghorn Cancer Centre, St. Vincent's Hospital, Medical Oncology, Garvan Institute of Medical Research, Sydney; Medical Oncology, University of New South Wales, Sydney, Australia.
  • Zhao Q; Merck & Co., Inc., Kenilworth.
  • Jensen E; Merck & Co., Inc., Kenilworth.
  • Ahsan S; Merck & Co., Inc., Kenilworth.
  • Ibrahim N; Merck & Co., Inc., Kenilworth.
  • Ribas A; Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, USA.
Ann Oncol ; 30(4): 582-588, 2019 04 01.
Article en En | MEDLINE | ID: mdl-30715153
BACKGROUND: Pembrolizumab demonstrated robust antitumor activity and safety in the phase Ib KEYNOTE-001 study (NCT01295827) of advanced melanoma. Five-year outcomes in all patients and treatment-naive patients are reported herein. Patients whose disease progressed following initial response and who received a second course of pembrolizumab were also analyzed. PATIENTS AND METHODS: Patients aged ≥18 years with previously treated or treatment-naive advanced/metastatic melanoma received pembrolizumab 2 mg/kg every 3 weeks, 10 mg/kg every 3 weeks, or 10 mg/kg every 2 weeks until disease progression, intolerable toxicity, or patient/investigator decision to withdraw. Kaplan-Meier estimates of overall survival (OS) and progression-free survival (PFS) were calculated. Objective response rate and PFS were based on immune-related response criteria by investigator assessment (data cut-off, September 1, 2017). RESULTS: KEYNOTE-001 enrolled 655 patients with melanoma; median follow-up was 55 months. Estimated 5-year OS was 34% in all patients and 41% in treatment-naive patients; median OS was 23.8 months (95% CI, 20.2-30.4) and 38.6 months (95% CI, 27.2-not reached), respectively. Estimated 5-year PFS rates were 21% in all patients and 29% in treatment-naive patients; median PFS was 8.3 months (95% CI, 5.8-11.1) and 16.9 months (95% CI, 9.3-35.5), respectively. Median response duration was not reached; 73% of all responses and 82% of treatment-naive responses were ongoing at data cut-off; the longest response was ongoing at 66 months. Four patients [all with prior response of complete response (CR)] whose disease progressed during observation subsequently received second-course pembrolizumab. One patient each achieved CR and partial response (after data cut-off). Treatment-related AEs (TRAEs) occurred in 86% of patients and resulted in study discontinuation in 7.8%; 17% experienced grade 3/4 TRAE. CONCLUSIONS: This 5-year analysis of KEYNOTE-001 represents the longest follow-up for pembrolizumab to date and confirms the durable antitumor activity and tolerability of pembrolizumab in advanced melanoma. CLINICAL TRIAL REGISTRY: ClinicalTrials.gov, NCT01295827.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Anticuerpos Monoclonales Humanizados / Antineoplásicos Inmunológicos / Melanoma Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Anticuerpos Monoclonales Humanizados / Antineoplásicos Inmunológicos / Melanoma Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article