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Antitumour Activity and Safety of Enzalutamide in Patients with Metastatic Castration-resistant Prostate Cancer Previously Treated with Abiraterone Acetate Plus Prednisone for ≥24 weeks in Europe.
de Bono, Johann S; Chowdhury, Simon; Feyerabend, Susan; Elliott, Tony; Grande, Enrique; Melhem-Bertrandt, Amal; Baron, Benoit; Hirmand, Mohammad; Werbrouck, Patrick; Fizazi, Karim.
Afiliación
  • de Bono JS; The Institute of Cancer Research, London, UK. Electronic address: johann.de-bono@icr.ac.uk.
  • Chowdhury S; Guy's Hospital, London, UK; King's Hospital, London, UK; St Thomas' Hospital, London, UK.
  • Feyerabend S; Studienpraxis Urologie, Nürtingen, Germany.
  • Elliott T; The Christie Hospital, Manchester, UK.
  • Grande E; Hospital Universitario Ramon y Cajal, Madrid, Spain.
  • Melhem-Bertrandt A; Astellas Pharma, Inc, Northbrook, IL, USA.
  • Baron B; Astellas Pharma, Inc, Leiden, the Netherlands.
  • Hirmand M; Medivation, Inc, which was acquired by Pfizer, Inc in September 2016, San Francisco, CA, USA.
  • Werbrouck P; AZ Groeninge, Kortrijk, Belgium.
  • Fizazi K; Institut Gustave Roussy, Paris-Sud University, Villejuif, France.
Eur Urol ; 74(1): 37-45, 2018 07.
Article en En | MEDLINE | ID: mdl-28844372
BACKGROUND: Enzalutamide and abiraterone acetate plus prednisone, which target the androgen receptor axis, have expanded the treatment of advanced prostate cancer. Retrospective analyses suggest some cross-resistance between these two drugs when used sequentially, but robust, prospective studies have not yet been reported. OBJECTIVE: To fulfil a regulatory postregistration commitment by evaluating the efficacy and safety of enzalutamide in patients with metastatic castration-resistant prostate cancer (mCRPC) who progressed following abiraterone acetate plus prednisone treatment. DESIGN, SETTING, AND PARTICIPANTS: Multicentre, single-arm, open-label study, enrolled patients with progressing mCRPC after ≥24 wk of abiraterone acetate plus prednisone treatment. All patients maintained castration therapy during the trial. Prior chemotherapy was allowed but not required. INTERVENTION: Patients received enzalutamide 160mg/d orally. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The primary endpoint was radiographic progression-free survival. Secondary endpoints were overall survival, prostate-specific antigen (PSA) response, and time-to-PSA progression. Safety data were also assessed. Kaplan-Meier methods were used to descriptively analyse time-to-event endpoints. RESULTS AND LIMITATIONS: Overall, 214 patients received enzalutamide treatment, 145 of whom were chemotherapy-naïve. Median radiographic progression-free survival was 8.1 mo (95% confidence interval: 6.1-8.3); median overall survival had not been reached. Unconfirmed PSA response rate was 27% (48 of 181). Median time-to-PSA progression was 5.7 mo (95% confidence interval: 5.6-5.8). The most common treatment-emergent adverse events were fatigue (32%), decreased appetite (25%), asthenia (18%), back pain (17%), and arthralgia (16%). No seizures were reported. CONCLUSIONS: Enzalutamide showed antitumour activity in some patients with mCRPC who had previously progressed following ≥24 wk of abiraterone acetate plus prednisone treatment. PATIENT SUMMARY: Patients with mCRPC who progressed on previous abiraterone acetate plus prednisone treatment, with or without prior chemotherapy, received enzalutamide. Although cross-resistance between the two agents was observed in a majority of patients, some still benefited from enzalutamide treatment.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feniltiohidantoína / Prednisona / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias de la Próstata Resistentes a la Castración / Acetato de Abiraterona / Antagonistas de Andrógenos Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Aged / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Eur Urol Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feniltiohidantoína / Prednisona / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias de la Próstata Resistentes a la Castración / Acetato de Abiraterona / Antagonistas de Andrógenos Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Aged / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Eur Urol Año: 2018 Tipo del documento: Article