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Bicalutamide (‘Casodex’) 150 mg in addition to standard care in patients with nonmetastatic prostate cancer: updated results from a randomised double-blind phase III study (median follow-up 5.1 y) in the early prostate cancer programme

Abstract

Trial 24 is one of three placebo-controlled trials within the ongoing bicalutamide (‘Casodex’) Early Prostate Cancer (EPC) programme evaluating bicalutamide 150 mg/day in addition to radical prostatectomy, radiotherapy or watchful waiting for T1b–4, any N, M0 prostate cancer. In Trial 24, at 5.1 y median follow-up, the addition of bicalutamide significantly (P<0.0001) improved objective progression-free survival (PFS) and prostate-specific antigen PFS compared with standard care alone. There was no significant difference in overall survival (P=0.746). In the context of the whole EPC programme, long-term bicalutamide is not appropriate for localised disease, yet provides advantages in delaying disease progression in patients with locally advanced prostate cancer.

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Acknowledgements

Editorial support was provided by Sarah Goodger, PhD; AstraZeneca provided financial assistance for this support.

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Correspondence to M Wirth.

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‘Casodex’ is a trademark of the AstraZeneca group of companies

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Wirth, M., Tyrrell, C., Delaere, K. et al. Bicalutamide (‘Casodex’) 150 mg in addition to standard care in patients with nonmetastatic prostate cancer: updated results from a randomised double-blind phase III study (median follow-up 5.1 y) in the early prostate cancer programme. Prostate Cancer Prostatic Dis 8, 194–200 (2005). https://doi.org/10.1038/sj.pcan.4500799

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