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Randomized phase III KEYNOTE-045 trial of pembrolizumab versus paclitaxel, docetaxel, or vinflunine in recurrent advanced urothelial cancer: results of >2 years of follow-up.
Fradet, Y; Bellmunt, J; Vaughn, D J; Lee, J L; Fong, L; Vogelzang, N J; Climent, M A; Petrylak, D P; Choueiri, T K; Necchi, A; Gerritsen, W; Gurney, H; Quinn, D I; Culine, S; Sternberg, C N; Nam, K; Frenkl, T L; Perini, R F; de Wit, R; Bajorin, D F.
Afiliación
  • Fradet Y; Department of Surgery/Urology, CHU de Québec-Université Laval, Québec City, Canada. Electronic address: yves.fradet@crchudequebec.ulaval.ca.
  • Bellmunt J; Department of Medical Oncology, PSMAR-IMIM Research Institute, Barcelona, Spain and Harvard Medical School University, Boston, USA.
  • Vaughn DJ; Department of Medical Oncology, Abramson Cancer Center, Perelman Center for Advanced Medicine, Philadelphia, USA.
  • Lee JL; Department of Oncology, Asan Medical Center and University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Fong L; Department of Medicine and Urology, University of California San Francisco, San Francisco.
  • Vogelzang NJ; Department of Medical Oncology, Comprehensive Cancer Centers of Nevada, Las Vegas, USA.
  • Climent MA; Department of Medical Oncology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
  • Petrylak DP; Division of Medical Oncology, Smilow Cancer Hospital at Yale University, New Haven.
  • Choueiri TK; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, USA.
  • Necchi A; Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Gerritsen W; Department of Medical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Gurney H; Department of Medical Oncology, Westmead Hospital and Macquarie University, Sydney, NSW, Australia.
  • Quinn DI; Department of Medical Oncology, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, USA.
  • Culine S; Department of Medical Oncology, Hôpital Saint-Louis, Paris, France.
  • Sternberg CN; Department of Medical Oncology, Englander Institute for Precision Medicine, Weill Cornell Medicine, New York-Presbyterian, New York.
  • Nam K; Department of Medical Oncology, Merck & Co., Inc., Kenilworth, USA.
  • Frenkl TL; Department of Medical Oncology, Merck & Co., Inc., Kenilworth, USA.
  • Perini RF; Department of Medical Oncology, Merck & Co., Inc., Kenilworth, USA.
  • de Wit R; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Bajorin DF; Department of Medical Oncology, Memorial Sloan Kettering Cancer Center, New York, USA.
Ann Oncol ; 30(6): 970-976, 2019 06 01.
Article en En | MEDLINE | ID: mdl-31050707
ABSTRACT

BACKGROUND:

Novel second-line treatments are needed for patients with advanced urothelial cancer (UC). Interim analysis of the phase III KEYNOTE-045 study showed a superior overall survival (OS) benefit of pembrolizumab, a programmed death 1 inhibitor, versus chemotherapy in patients with advanced UC that progressed on platinum-based chemotherapy. Here we report the long-term safety and efficacy outcomes of KEYNOTE-045. PATIENTS AND

METHODS:

Adult patients with histologically/cytologically confirmed UC whose disease progressed after first-line, platinum-containing chemotherapy were enrolled. Patients were randomly assigned 1  1 to receive pembrolizumab [200 mg every 3 weeks (Q3W)] or investigator's choice of paclitaxel (175 mg/m2 Q3W), docetaxel (75 mg/m2 Q3W), or vinflunine (320 mg/m2 Q3W). Primary end points were OS and progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1) by blinded independent central radiology review (BICR). A key secondary end point was objective response rate per RECIST v1.1 by BICR.

RESULTS:

A total of 542 patients were enrolled (pembrolizumab, n = 270; chemotherapy, n = 272). Median follow-up as of 26 October 2017 was 27.7 months. Median 1- and 2-year OS rates were higher with pembrolizumab (44.2% and 26.9%, respectively) than chemotherapy (29.8% and 14.3%, respectively). PFS rates did not differ between treatment arms; however, 1- and 2-year PFS rates were higher with pembrolizumab. The objective response rate was also higher with pembrolizumab (21.1% versus 11.0%). Median duration of response to pembrolizumab was not reached (range 1.6+ to 30.0+ months) versus chemotherapy (4.4 months; range 1.4+ to 29.9+ months). Pembrolizumab had lower rates of any grade (62.0% versus 90.6%) and grade ≥3 (16.5% versus 50.2%) treatment-related adverse events than chemotherapy.

CONCLUSIONS:

Long-term results (>2 years' follow-up) were consistent with those of previously reported analyses, demonstrating continued clinical benefit of pembrolizumab over chemotherapy for efficacy and safety for treatment of locally advanced/metastatic, platinum-refractory UC. TRIAL REGISTRATION ClinicalTrials.gov NCT02256436.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Urológicas / Recurrencia Local de Neoplasia Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Urológicas / Recurrencia Local de Neoplasia Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article