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Subsequent Chemotherapy and Treatment Patterns After Abiraterone Acetate in Patients with Metastatic Castration-resistant Prostate Cancer: Post Hoc Analysis of COU-AA-302.
de Bono, Johann S; Smith, Matthew R; Saad, Fred; Rathkopf, Dana E; Mulders, Peter F A; Small, Eric J; Shore, Neal D; Fizazi, Karim; De Porre, Peter; Kheoh, Thian; Li, Jinhui; Todd, Mary B; Ryan, Charles J; Flaig, Thomas W.
Afiliación
  • de Bono JS; The Institute of Cancer Research and The Royal Marsden Hospital, Sutton, UK. Electronic address: johann.de-bono@icr.ac.uk.
  • Smith MR; Harvard Medical School and Massachusetts General Hospital, Boston, MA, USA.
  • Saad F; Centre Hospitalier University of Montréal, Montréal, Québec, Canada.
  • Rathkopf DE; Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, NY, USA.
  • Mulders PFA; Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Small EJ; Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA.
  • Shore ND; Carolina Urologic Research Center, Atlantic Urology Clinics, Myrtle Beach, SC, USA.
  • Fizazi K; Institut Gustave Roussy, University of Paris Sud, Villejuif, France.
  • De Porre P; Janssen Research & Development, Beerse, Belgium.
  • Kheoh T; Janssen Research & Development, San Diego, CA, USA.
  • Li J; Johnson & Johnson Medical China, Shanghai, China.
  • Todd MB; Janssen Global Services, Raritan, NJ, USA.
  • Ryan CJ; Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA.
  • Flaig TW; University of Colorado Cancer Center, Aurora, CO, USA.
Eur Urol ; 71(4): 656-664, 2017 04.
Article en En | MEDLINE | ID: mdl-27402060
ABSTRACT

BACKGROUND:

Treatment patterns for metastatic castration-resistant prostate cancer (mCRPC) have changed substantially in the last few years. In trial COU-AA-302 (chemotherapy-naïve men with mCRPC), abiraterone acetate plus prednisone (AA) significantly improved radiographic progression-free survival and overall survival (OS) when compared to placebo plus prednisone (P).

OBJECTIVE:

This post hoc analysis investigated clinical responses to docetaxel as first subsequent therapy (FST) among patients who progressed following protocol-specified treatment with AA, and characterized subsequent treatment patterns among older (≥75 yr) and younger (<75 yr) patient subgroups. DESIGN, SETTING, AND

PARTICIPANTS:

Data were collected at the final OS analysis (96% of expected death events). Subsequent therapy data were prospectively collected, while response and discontinuation data were collected retrospectively following discontinuation of the study drug. INTERVENTION At the discretion of the investigator, 67% (365/546) of patients from the AA arm received subsequent treatment with one or more agents approved for mCRPC. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

Efficacy analysis was performed for patients for whom baseline and at least one post-baseline prostate-specific antigen (PSA) values were available. RESULTS AND

LIMITATIONS:

Baseline and at least one post-baseline PSA values were available for 100 AA patients who received docetaxel as FST. While acknowledging the limitations of post hoc analyses, 40% (40/100) of these patients had an unconfirmed ≥50% PSA decline with first subsequent docetaxel therapy, and 27% (27/100) had a confirmed ≥50% PSA decline. The median docetaxel treatment duration among these 100 patients was 4.2 mo. Docetaxel was the most common FST among older and younger patients from each treatment arm. However, 43% (79/185) of older patients who progressed on AA received no subsequent therapy for mCRPC, compared with 17% (60/361) of younger patients.

CONCLUSIONS:

Patients with mCRPC who progress with AA treatment may still derive benefit from subsequent docetaxel therapy. These data support further assessment of treatment patterns following AA treatment for mCRPC, particularly among older patients. TRIAL REGISTRATION ClinicalTrials.gov NCT00887198. PATIENT

SUMMARY:

Treatment patterns for advanced prostate cancer have changed substantially in the last few years. This additional analysis provides evidence of clinical benefit for subsequent chemotherapy in men with advanced prostate cancer whose disease progressed after treatment with abiraterone acetate. Older patients were less likely to be treated with subsequent therapy.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Carcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Taxoides / Neoplasias de la Próstata Resistentes a la Castración / Antineoplásicos Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies Idioma: En Revista: Eur Urol Año: 2017 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Carcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Taxoides / Neoplasias de la Próstata Resistentes a la Castración / Antineoplásicos Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies Idioma: En Revista: Eur Urol Año: 2017 Tipo del documento: Article