Abstract

SummaryBackgroundSome studies have suggested a link between antihypertensive medication and cancer, but the evidence is so far inconclusive. Thus, we aimed to investigate this association in a large individual patient data meta-analysis of randomised clinical trials.MethodsWe searched PubMed, MEDLINE, The Cochrane Central Register of Controlled Trials, and ClinicalTrials.gov from Jan 1, 1966, to Sept 1, 2019, to identify potentially eligible randomised controlled trials. Eligible studies were randomised controlled trials comparing one blood pressure lowering drug class with a placebo, inactive control, or other blood pressure lowering drug. We also required that trials had at least 1000 participant years of follow-up in each treatment group. Trials without cancer event information were excluded. We requested individual participant data from the authors of eligible trials. We pooled individual participant-level data from eligible trials and assessed the effects of angiotensin-converting enzyme inhibitors (ACEIs), angiotensin II receptor blockers (ARBs), β blockers, calcium channel blockers, and thiazide diuretics on cancer risk in one-stage individual participant data and network meta-analyses. Cause-specific fixed-effects Cox regression models, stratified by trial, were used to calculate hazard ratios (HRs). The primary outcome was any cancer event, defined as the first occurrence of any cancer diagnosed after randomisation. This study is registered with PROSPERO (CRD42018099283).Findings33 trials met the inclusion criteria, and included 260 447 participants with 15 012 cancer events. Median follow-up of included participants was 4·2 years (IQR 3·0–5·0). In the individual participant data meta-analysis comparing each drug class with all other comparators, no associations were identified between any antihypertensive drug class and risk of any cancer (HR 0·99 [95% CI 0·95–1·04] for ACEIs; 0·96 [0·92–1·01] for ARBs; 0·98 [0·89–1·07] for β blockers; 1·01 [0·95–1·07] for thiazides), with the exception of calcium channel blockers (1·06 [1·01–1·11]). In the network meta-analysis comparing drug classes against placebo, we found no excess cancer risk with any drug class (HR 1·00 [95% CI 0·93–1·09] for ACEIs; 0·99 [0·92–1·06] for ARBs; 0·99 [0·89–1·11] for β blockers; 1·04 [0·96–1·13] for calcium channel blockers; 1·00 [0·90–1·10] for thiazides).InterpretationWe found no consistent evidence that antihypertensive medication use had any effect on cancer risk. Although such findings are reassuring, evidence for some comparisons was insufficient to entirely rule out excess risk, in particular for calcium channel blockers.FundingBritish Heart Foundation, National Institute for Health Research, Oxford Martin School.

Highlights

  • Evidence for the benefits of antihypertensive medication in the prevention of cardiovascular disease is well established,[1] low adherence to treatment is a major barrier to effective blood pressure control.[2]

  • We found no evidence of an association between antihypertensive drugs and any cancer when assessing all comparison groups, with the exception of calcium channel blockers (1·06 [1·01–1·11]; figure 1A)

  • We examined the effects of antihypertensive drug classes on risks of breast, colorectal, lung, prostate, and skin cancer compared with all other comparators

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Summary

Introduction

Evidence for the benefits of antihypertensive medication in the prevention of cardiovascular disease is well established,[1] low adherence to treatment is a major barrier to effective blood pressure control.[2]. A series of meta-analyses of randomised controlled trials, based on aggregate data, have investigated the association between class-specific antihypertensive treatment and risk of cancer, but findings have been conflicting. One study has suggested that using ARBs increases the risk of cancer,[4] whereas two subsequent meta-analyses showed no such association.[11,12] Another meta-analysis of randomised controlled trials found no evidence linking any drug class with the incidence of any cancer,[12] but an increased risk of cancer with the use of angiotensin-converting enzyme inhibitors (ACEIs) in combination with ARBs could not be ruled out.

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