Key result
Angiotensin receptor blocker therapy is not associated with an increased risk of new cancer occurrence or cancer-related death.
Why the study?
Does angiotensin receptor blocker therapy increase the risk of new cancer occurrence or cancer-related death in patients with hypertension, heart failure, and/or nephropathy?
Does angiotensin receptor blocker therapy increase the risk of new cancer occurrence or cancer-related death in patients with hypertension, heart failure, and/or nephropathy?
This review reassures clinicians that ARB therapy is not associated with an increased risk of cancer or cancer-related death.
Answers are grounded in this paper and cite their sources.
Supports ARB safety on cancer risk in hypertension and HF; leaves open need for prospective randomized confirmation.
The role of drugs in new cancer occurrence and cancer-related death is a major concern. Recently, a meta-analysis raised the possibility that angiotensin receptor blockers (ARBs) might have an adverse effect on patients. This generated a significant debate until the publication of two further meta-analyses, neither of which demonstrated an increased risk of new cancer occurrence or cancer-related death with the use of ARBs in patients with hypertension, heart failure, and/or nephropathy. This illustrates that the results of meta-analyses should be interpreted cautiously and critically as bias, such as selection bias, might lead to erroneous conclusions. Overall, the bulk of evidence today indicates that ARBs are not associated with increased cancer risk.
No takes yet. Share an insight, caveat, or question.
Waeber et al. (2011) conducted a review in hypertension, heart failure, and/or nephropathy. Angiotensin receptor blockers (ARBs) was evaluated on new cancer occurrence or cancer-related death. Angiotensin receptor blocker therapy is not associated with an increased risk of new cancer occurrence or cancer-related death.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: