Androgen deprivation therapy prevents bladder cancer recurrence
Author(s) -
Koji Izumi,
Masataka Taguri,
Hiroshi Miyamoto,
Yoshinori Hara,
Takeshi Kishida,
Kimio Chiba,
Tetsuo Murai,
Kotaro Hirai,
Kotaro Suzuki,
Kiyoshi Fujinami,
Teiichiro Ueki,
Koichi Udagawa,
Kazuo Kitami,
Masatoshi Moriyama,
Yasuhide Miyoshi,
Futoshi Tsuchiya,
Ichiro Ikeda,
Kazuki Kobayashi,
Maho Sato,
Satoshi Morita,
Kazumi Noguchi,
Hiroji Uemura
Publication year - 2014
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.2851
Subject(s) - medicine , androgen deprivation therapy , bladder cancer , prostate cancer , oncology , biochemical recurrence , urology , cancer , prostatectomy
Although accumulating preclinical evidence indicates the involvement of androgen receptor signals in bladder cancer (BC) development, its clinical relevance remains unclear. We aimed to evaluate the predictive role of androgen deprivation therapy (ADT) in BC recurrence in prostate cancer (PC) patients. We retrospectively reviewed 20,328 patients with PC diagnosed during 1991-2013 and identified 239 (1.2%) men having primary BC. After excluding ineligible patients, 162 patients made up a final cohort. With a median follow-up of 62 months, 38 (50%) of 76 control patients without ADT experienced BC recurrence, while 19 (22%) of 86 did in ADT group. Thus, patients having received ADT for their PC showed a significantly lower risk of BC recurrence (5-year actuarial recurrence-free survival: 76% v 40%; P < 0.001) and also had a significantly smaller number of recurrence episodes (5-year cumulative recurrence: 0.44 v 1.54; P < 0.001), compared to the control patients. A multivariable analysis revealed ADT as an independent prognosticator (hazard ratio, 0.29; 95% confidence interval, 0.17-0.49) for BC recurrence. This is the first clinical study showing that ADT significantly reduces the risk of BC recurrence.
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