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Survival benefit of early androgen receptor inhibitor therapy in locally advanced prostate cancer : Long-term follow-up of the SPCG-6 study

Thomsen, Frederik B. (author)
Dept Urol, Copenhagen Prostate Canc Ctr, Rigshosp, Univ Copenhagen, Copenhagen, Denmark
Brasso, Klaus (author)
Dept Urol, Copenhagen Prostate Canc Ctr, Rigshosp, Univ Copenhagen, Copenhagen, Denmark
Christensen, Ib J. (author)
Copenhagen Bioctr, Finsen Lab, Rigshosp, Univ Copenhagen, Copenhagen, Denmark; Biotech Res & Innovat Ctr, Rigshosp, Univ Copenhagen, Copenhagen, Denmark
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Johansson, Jan-Erik (author)
Department, Sch Hlth & Med Sci, Dept Urol, Örebro Univ, Örebro, Sweden
Angelsen, Anders (author)
Fac Med, Norwegian Univ Sci & Technol, Trondheim, Norway
Tammela, Teuvo L. J. (author)
Dept Surg, Tampere Univ Hosp, Tampere, Finland;Sch Med, Univ Tampere, Tampere, Finland
Iversen, Peter (author)
Dept Urol, Copenhagen Prostate Canc Ctr, Rigshosp, Univ Copenhagen, Copenhagen, Denmark
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 (creator_code:org_t)
Elsevier BV, 2015
2015
English.
In: European Journal of Cancer. - : Elsevier BV. - 0959-8049 .- 1879-0852. ; 51:10, s. 1283-1292
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: The optimal timing of endocrine therapy in non-metastatic prostate cancer (PCa) is still an issue of debate. Methods: A randomised, double-blind, parallel-group trial comparing bicalutamide 150 mg once daily with placebo in addition to standard care in patients with hormone-naive, non-metastatic PCa. Kaplan-Meier analysis was used to estimate overall survival (OS) and multivariate Cox proportional hazard model was performed to analyse time-to-event (death). Findings: A total of 1218 patients were included into the Scandinavian Prostate Cancer Group (SPCG)-6 study of which 607 were randomised to receive bicalutamide in addition to their standard care and 611 to receive placebo. Median follow-up was 14.6 years. Overall, 866 (71.1%) patients died, 428 (70.5%) in the bicalutamide arm and 438 (71.7%) in the placebo arm, p = 0.87. Bicalutamide significantly improved OS in patient with locally advanced disease (hazard ratios (HR) = 0.77 (95% confidence interval (CI): 0.63-0.94, p = 0.01), regardless of baseline prostate-specific antigen (PSA), with a survival benefit which was apparent throughout the study period. In contrast, survival favoured randomisation to the placebo arm in patients with localised disease (HR = 1.19 (95% CI: 1.00-1.43), p = 0.056). However, a survival gain from bicalutamide therapy was present in patients with localised disease and a baseline PSA greater than 28 ng/mL at randomisation. In multivariate Cox proportional hazard model, only including patients managed on watchful waiting as their standard of care (n = 991) OS depended on age, World Health Organisation (WHO) grade, baseline PSA, clinical stage and randomised treatment. Interpretation: Throughout the 14.6 year follow-up period the addition of early bicalutamide to standard of care resulted in a significant OS benefit in patients with locally advanced PCa. In contrast, patients with localised PCa and low PSA derived no survival benefit from early bicalutamide. The optimal timing for initiating bicalutamide in non-metastatic PCa patients is dependent on disease stage and baseline PSA. (C) 2015 Elsevier Ltd. All rights reserved.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Antiandrogen
Bicalutamide
Localised
Locally advanced
Prostate cancer
Survival

Publication and Content Type

ref (subject category)
art (subject category)

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