Beta-blockers improve survival outcomes in patients with multiple myeloma: a retrospective evaluation

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• 作者：Yi L. Hwa ; Qian Shi ; Shaji K. Kumar ; Martha Q. Lacy ; Morie A. Gertz ; Prashant Kapoor ; Francis K. Buadi ; Nelson Leung ; David Dingli ; Ronald S. Go ; Suzanne R. Hayman ; Wilson I. Gonsalves ; Stephen Russell ; John A. Lust ; Yi Lin ; S. Vincent Rajkumar and Angela Dispenzieri
• 刊名：American Journal of Hematology
• 出版年：2017
• 出版时间：January 2017
• 年：2017
• 卷：92
• 期：1
• 页码：50-55
• 全文大小：520K
• ISSN：1096-8652

文摘

A preclinical study demonstrated anti-proliferative and apoptotic effect of propranolol on multiple myeloma (MM) cell. Clinical studies suggested that beta-blocker (BB) might impact the prognosis of breast, prostate, colorectal, ovarian, lung, and skin cancer. This retrospective study evaluated the effect of BB in MM disease-specific survival (DSS) and overall survival (OS). Among 1,971 newly diagnosed MM patients seen at Mayo Clinic between 1995 and 2010, usage of BB and other cardiac (or antihypertensive) medications were abstracted. Cumulative incidence function and Kaplan–Meier method were used to estimate 5-year cumulative incidence rate (CIR) of MM death and OS rate, respectively. Nine hundred and thirty (47.2%) patients had no intake of cardiac medications; 260 (13.2%) used BB alone; 343 (17.4%) used both BB/non-BB cardiac medications; and 438 (22.2%) had non-BB cardiac drugs. Superior MM DSS was observed in BB only users, compared to patients without any cardiac drugs ( HRadj.CS, 0.53, 95% confidence interval [CI], 0.42–0.67, P_adj.<0.0001) and non-BB cardiac drugs users ( HRadj.CS, 0.49, 95% CI, 0.38–0.63, P_adj.<0.0001). Patients on both BB and other cardiac drugs showed superior DSS than non-cardiac drugs users ( HRadj.CS, 0.54, 95% CI, 0.44–0.67, P_adj.<0.0001) and non-BB cardiac drug users. ( HRadj.CS, 0.50, 95% CI, 0.40–0.62, P_adj.<0.0001). MM DSS did not differ between BB users with and without other cardiac drugs (P_adj.=0.90). Multivariable analysis showed the same pattern for OS. In patients with MM, BB intake is associated with a reduced risk of disease-specific death and overall mortality in comparison to non-BB or no use of cardiac drugs. Am. J. Hematol. 92:50–55, 2017.