Iwagami Masao, Kumazawa Ryosuke, Miyamoto Yoshihisa, Ito Yuri, Ishimaru Miho, Morita Kojiro, Hamada Shota, Tamiya Nanako, Yasunaga Hideo
Department of Health Services Research, Faculty of Medicine, Institutes of Medicine, University of Tsukuba, Building #861, 1-1-1 Tenno-dai, Tsukuba, Ibaraki, Japan.
Department of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK.
Drug Saf. 2021 Mar;44(3):361-371. doi: 10.1007/s40264-020-01024-0. Epub 2020 Nov 27.
In September 2019, ranitidine and nizatidine were suggested to contain N-nitrosodimethylamine, a carcinogenic substance. People have since been concerned about the potential impact of ranitidine/nizatidine use on the risk of cancer.
The objective of this study was to investigate the risk of cancer among people receiving ranitidine or nizatidine compared with other histamine 2 receptor antagonists (H2 blockers) [cimetidine, famotidine, roxatidine, and lafutidine].
In the Japan Medical Data Center claims database (comprising people aged < 75 years) from 2005 to 2018, we identified new adult users of H2 blockers and classified them into ranitidine/nizatidine users and other H2 blocker users. We estimated the incidence of cancer diagnosis in each group and conducted a multivariable Cox regression analysis.
We identified 113,745 new users of ranitidine/nizatidine (median age 41.2 years [interquartile range 31.7-51.1]; 49.1% men; median follow-up 2.4 years [1.1-4.5]) and 503,982 new users of other H2 blockers (median age 40.9 years [31.1-51.2]; 51.0% men; median follow-up 2.3 years [0.9-4.2]). The incidence rate of cancer diagnosis was 6.39 (95% confidence interval 6.13-6.66) cases per 1000 person-years (top three sites: breast 14.8%; colorectal 14.6%; and stomach 11.5%) in the ranitidine/nizatidine group and 6.17 (6.05-6.30) cases per 1000 person-years (colorectal 14.7%; breast 13.5%; and stomach 11.2%) in the other H2 blockers group. The adjusted hazard ratio (ranitidine/nizatidine users vs other H2 blocker users) was 1.02 (0.98-1.07). The results were similar by follow-up length, by cancer site, and when ranitidine and nizatidine users were separately compared with the other H2 blockers group. By cumulative dose, the adjusted hazard ratio (95% confidence interval) was 1.03 (0.98-1.08) from 1 to 180 defined daily doses (DDDs), 1.00 (0.73-1.39) from 181 to 365 DDDs, 0.95 (0.61-1.48) from 366 to 730 DDDs, and 0.83 (0.45-1.55) at > 730 DDDs.
We found no evidence that ranitidine/nizatidine is associated with an increased risk of cancer, although further studies with more accurate measurement of exposure, inclusion of older people, and longer follow-up may be needed.
2019年9月,有人提出雷尼替丁和尼扎替丁含有致癌物质N-亚硝基二甲胺。自那时起,人们一直关注使用雷尼替丁/尼扎替丁对癌症风险的潜在影响。
本研究的目的是调查接受雷尼替丁或尼扎替丁治疗的人群与其他组胺2受体拮抗剂(H2阻滞剂)[西咪替丁、法莫替丁、罗沙替丁和拉呋替丁]相比的癌症风险。
在2005年至2018年的日本医学数据中心索赔数据库(包括年龄<75岁的人群)中,我们确定了H2阻滞剂的新成年使用者,并将他们分为雷尼替丁/尼扎替丁使用者和其他H2阻滞剂使用者。我们估计了每组癌症诊断的发生率,并进行了多变量Cox回归分析。
我们确定了113745名雷尼替丁/尼扎替丁的新使用者(中位年龄41.2岁[四分位间距31.7 - 51.1];49.1%为男性;中位随访2.4年[1.1 - 4.5])和503982名其他H2阻滞剂的新使用者(中位年龄40.9岁[31.1 - 51.2];51.0%为男性;中位随访2.3年[0.9 - 4.2])。雷尼替丁/尼扎替丁组癌症诊断的发生率为每1000人年6.39例(95%置信区间6.13 - 6.66)(前三位部位:乳腺癌14.8%;结直肠癌14.6%;胃癌11.5%),其他H2阻滞剂组为每1000人年6.17例(6.05 - 6.30)(结直肠癌14.7%;乳腺癌13.5%;胃癌11.2%)。调整后的风险比(雷尼替丁/尼扎替丁使用者与其他H2阻滞剂使用者相比)为1.02(0.98 - 1.07)。按随访时间长短、癌症部位以及将雷尼替丁和尼扎替丁使用者分别与其他H2阻滞剂组进行比较时,结果相似。按累积剂量计算,调整后的风险比(95%置信区间)在1至180限定日剂量(DDD)时为1.03(0.98 - 1.08),181至365 DDD时为1.00(0.73 - 1.39),366至730 DDD时为0.95(0.61 - 1.48),>730 DDD时为0.83(0.45 - 1.55)。
我们没有发现证据表明雷尼替丁/尼扎替丁与癌症风险增加有关,尽管可能需要进行更准确测量暴露情况、纳入老年人以及延长随访时间的进一步研究。