Fujimoto Mai, Kanou Migiwa, Hosomi Kouichi, Takada Mitsutaka
Int J Clin Pharmacol Ther. 2017 Apr;55(4):295-303. doi: 10.5414/CP202842.
The aim of this study was to examine the associations between angiotensin receptor blockers (ARBs) and the risk of 10 major cancers by employing different pharmacoepidemiological assessments.
Data from the first quarter of 2004 through 2012 were downloaded from the US Food and Drug Administration Adverse Event Reporting System (FAERS). The reporting odds ratio (ROR) and information component (IC) were used to detect the signals. Furthermore, symmetry analysis was applied to the claims database to identify the risk of cancer after using ARBs from January 2005 to July 2013.
Significant inverse associations were found for all cancer types assessed as a whole (ROR: 0.78, 95% confidence interval (CI): 0.75 - 0.80; IC: -0.36, 95% CI: -0.40 to -0.31) in the analyses of FAERS database. Likewise, significant inverse association was found for all cancer types assessed as a whole (adjusted sequence ratio: 0.89, 95% CI: 0.82 - 0.96) in claims database. In addition, a significantly decreased risk for breast cancer and increased risks for pancreatic and prostate cancer were found in patients treated with ARBs in the analyses of individual cancers.
CONCLUSIONS: Significant inverse association was found between ARB use and all cancer types assessed as a whole. However, in the analyses of individual cancers, the risks of ARB-induced cancer may differ according to cancer site. It may be reasonable to assume that the risks of ARB-induced cancer may differ according to cancer site. .
本研究旨在通过采用不同的药物流行病学评估方法,探讨血管紧张素受体阻滞剂(ARB)与10种主要癌症风险之间的关联。
从美国食品药品监督管理局不良事件报告系统(FAERS)下载2004年第一季度至2012年的数据。采用报告比值比(ROR)和信息成分(IC)来检测信号。此外,对索赔数据库进行对称性分析,以确定2005年1月至2013年7月使用ARB后患癌症的风险。
在FAERS数据库分析中,整体评估的所有癌症类型均发现显著的负相关(ROR:0.78,95%置信区间(CI):0.75 - 0.80;IC:-0.36,95%CI:-0.40至-0.31)。同样,在索赔数据库中,整体评估的所有癌症类型也发现显著的负相关(调整序列比:0.89,95%CI:0.82 - 0.96)。此外,在个体癌症分析中,使用ARB治疗的患者中乳腺癌风险显著降低,胰腺癌和前列腺癌风险增加。
发现ARB使用与整体评估的所有癌症类型之间存在显著的负相关。然而,在个体癌症分析中,ARB诱发癌症的风险可能因癌症部位而异。可以合理假设,ARB诱发癌症的风险可能因癌症部位而异。