Beta-blocker usage and prostate cancer survival: A nested case-control study in the UK Clinical Practice Research Datalink cohort

被引:37
作者
Cardwell, Chris R. [1 ]
Coleman, Helen G. [1 ]
Murray, Liam J. [1 ]
O'Sullivan, Joe M. [2 ,3 ]
Powe, Des G. [4 ,5 ]
机构
[1] Queens Univ Belfast, Ctr Publ Hlth, Canc Epidemiol & Hlth Serv Res Grp, Belfast BT7 1NN, Antrim, North Ireland
[2] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Belfast BT7 1NN, Antrim, North Ireland
[3] Belfast Hlth & Social Care Trust, Northern Ireland Canc Ctr, Belfast, Antrim, North Ireland
[4] Nottingham Univ Hosp NHS Trust, Queens Med Ctr, Dept Cellular Pathol, Nottingham NG7 2UH, England
[5] Nottingham Trent Univ, John van Geest Canc Res Ctr, Nottingham NG11 8NS, England
关键词
Beta-blocker; Prostate cancer; Mortality; AUSTLID TASKEN. ASSOCIATION; HELENE HARTVEDT GRYTLI; MORTEN WANG FAGERLAND; DISEASE. EUR UROL; SOPHIE D. FOSSA; BREAST-CANCER; PRESS; HTTP//DX.DOI.ORG/10.1016/J.EURURO.2013.01.007; METASTASIS DEVELOPMENT; HIGH-RISK; THERAPY;
D O I
10.1016/j.canep.2014.03.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Recent laboratory and epidemiological evidence suggests that beta-blockers could inhibit prostate cancer progression. Methods: We investigated the effect of beta-blockers on prostate cancer-specific mortality in a cohort of prostate cancer patients. Prostate cancer patients diagnosed between 1998 and 2006 were identified from the UK Clinical Practice Research Database and confirmed by cancer registries. Patients were followed up to 2011 with deaths identified by the Office of National Statistics. A nested case-control analysis compared patients dying from prostate cancer (cases) with up to three controls alive at the time of their death, matched by age and year of diagnosis. Odds ratios (OR) and 95% confidence intervals (CI) were calculated using conditional logistic regression. Results: Post-diagnostic beta-blocker use was identified in 25% of 1184 prostate cancer-specific deaths and 26% of 3531 matched controls. There was little evidence (P = 0.40) of a reduction in the risk of cancer-specific death in beta-blocker users compared with non-users (OR = 0.94 95% CI 0.81, 1.09). Similar results were observed after adjustments for confounders, in analyses by beta-blocker frequency, duration, type and for all-cause mortality. Conclusions: Beta-blocker usage after diagnosis was not associated with cancer-specific or all-cause mortality in prostate cancer patients in this large UK study. (C) 2014 Published by Elsevier Ltd.
引用
收藏
页码:279 / 285
页数:7
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