Androgen Deprivation Therapy and Cardiovascular Risk in Chinese Patients with Nonmetastatic Carcinoma of Prostate. (7th April 2014)

• Record Type: Journal Article
• Authors: Huang, Gang; Yeung, Chun-Yip; Lee, Ka Kui; Liu, Jianxiong; Ho, Kwan Lun; Yiu, Ming-Kwong; Lam, Karen Siu-Ling; Tse, Hung-Fat; Yau, Thomas; Siu, Chung-Wah
• Other Names: Baguley Bruce C. Academic Editor.
• Is Part Of: Journal of oncology. Volume 2014(2014)
• Publication Date: 2014-04-07
• Subjects: Oncology -- Research -- Periodicals; Tumors -- Periodicals; Neoplasms; Oncology -- Research; Tumors; Periodicals; Periodicals; 616.994
• DOI: 10.1155/2014/529468
• Languages: English
• ISSNs: 1687-8450

Abstract

Abstract : Background . Androgen deprivation therapy (ADT) in nonmetastatic prostate cancer is unclear. Recent data suggests possible increase in the cardiovascular risks receiving ADT. The aim of the study was to investigate the cardiovascular outcomes in a cohort of Chinese nonmetastatic prostate cancer patients with no previously documented cardiovascular disease. Methods and Results . 745 patients with no previously documented cardiovascular disease and/or diabetes mellitus diagnosed to have nonmetastatic prostate cancer were recruited. Of these, 517 patients received ADT and the remaining 228 did not. After a mean follow-up of 5.3 years, 60 patients developed primary composite endpoint including (1) coronary artery disease, (2) congestive heart failure, and (3) ischemic stroke. Higher proportion of patients on ADT (51 patients, 9.9%) developed composite endpoint compared with those not on ADT (9 patients, 3.9%) with hazard ratio (HR) of 2.06 (95% confidence interval (CI): 1.03–3.24, P = 0.04 ). Furthermore, Cox regression analysis revealed that only the use of ADT (HR: 2.1, 95% CI: 1.03–4.25, P = 0.04 ) and hypertension (HR: 2.0, 95% CI: 1.21–3.33, P < 0.01 ) were independent predictors for primary composite endpoint. Conclusion . ADT in Chinese patients with nonmetastatic prostate cancer with no previously documented cardiovascular disease was associated with subsequent development of cardiovascular events.