Morales Daniel R, Pacurariu Alexandra, Slattery Jim, Kurz Xavier
Wellcome Trust Clinical Research Fellow, Division of Population Health and Genomics, University of Dundee, UK.
Pharmacovigilance and Epidemiology Department, European Medicines Agency, Amsterdam, Netherlands.
Br J Clin Pharmacol. 2020 Jul;86(7):1336-1345. doi: 10.1111/bcp.14245. Epub 2020 Mar 2.
Hydrochlorothiazide-induced photosensitivity may increase squamous cell carcinoma (SCC), basal cell carcinoma (BCC) and lip cancer risk. The aim was to quantify these risks.
Nested case-control studies using data from the UK THIN database from 01 January 1999 to 01 May 2016. Adults with incident SCC, BCC, melanoma, lip cancer and oral cancer were matched (on age, sex and calendar year of cohort entry) to controls using incidence density sampling. Incidence rate ratios (IRR) for each outcome were calculated for ever and cumulative hydrochlorothiazide exposure, measuring the impact of additionally adjusting for smoking and body mass index (BMI). Adjusted rate differences were estimated, including the number needed to harm.
Cumulative hydrochlorothiazide doses ≥50 000 mg were associated with a significantly increased risk of SCC IRR = 3.05 (1.93-4.81) and BCC IRR = 1.34 (1.06-1.69). Using a 5-year lag-period, hydrochlorothiazide exposure was also associated with a significantly increased risk of lip cancer (IRR 2.85, 95% confidence interval 1.32-6.15). No significantly increased risk of melanoma or oral cavity cancer was observed. Following adjustment for smoking and BMI, which had inverse associations with several skin cancer types, associations for hydrochlorothiazide remained significant. The overall number needed to harm with high-dose cumulative hydrochlorothiazide exposure was: 804 for SCC; 2463 for BCC, and 200 000 for lip cancer but varied by age and sex.
Hydrochlorothiazide exposure was associated with an increased risk of SCC, BCC and lip cancer that is not explained following adjustment for smoking and BMI. These findings may support clinical and regulatory decision making.
氢氯噻嗪诱发的光敏反应可能会增加鳞状细胞癌(SCC)、基底细胞癌(BCC)和唇癌的风险。本研究旨在量化这些风险。
采用巢式病例对照研究,数据来源于1999年1月1日至2016年5月1日的英国THIN数据库。采用发病密度抽样,将发生SCC、BCC、黑色素瘤、唇癌和口腔癌的成年人(按年龄、性别和队列进入日历年)与对照进行匹配。计算每种结局的发病率比(IRR),以评估既往和累积氢氯噻嗪暴露情况,并衡量额外调整吸烟和体重指数(BMI)后的影响。估计调整后的率差,包括伤害所需人数。
累积氢氯噻嗪剂量≥50000mg与SCC风险显著增加相关(IRR = 3.05,1.93 - 4.81),与BCC风险显著增加相关(IRR = 1.34,1.06 - 1.69)。采用5年滞后期,氢氯噻嗪暴露也与唇癌风险显著增加相关(IRR 2.85,95%置信区间1.32 - 6.15)。未观察到黑色素瘤或口腔癌风险显著增加。在调整与几种皮肤癌类型呈负相关的吸烟和BMI后,氢氯噻嗪的相关性仍然显著。高剂量累积氢氯噻嗪暴露导致伤害的总体所需人数为:SCC为804;BCC为2463,唇癌为200000,但因年龄和性别而异。
氢氯噻嗪暴露与SCC、BCC和唇癌风险增加相关,在调整吸烟和BMI后这种相关性仍无法解释。这些发现可能有助于临床和监管决策。