American Journal of Cardiology
Volume 108, Issue 2 , Pages 294-301, 15 July 2011

Meta-Analysis of Randomized Controlled Trials on Effect of Angiotensin-Converting Enzyme Inhibitors on Cancer Risk

  • Ilke Sipahi, MD

      Affiliations

    • Harrington-McLaughlin Heart and Vascular Institute, University Hospitals Case Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio
    • Corresponding Author InformationCorresponding author: Tel: 216-844-1639; fax: 216-844-8954
  • ,
  • Josephine Chou, MD

      Affiliations

    • Harrington-McLaughlin Heart and Vascular Institute, University Hospitals Case Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio
  • ,
  • Prasun Mishra, MD

      Affiliations

    • Harrington-McLaughlin Heart and Vascular Institute, University Hospitals Case Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio
  • ,
  • Sara M. Debanne, PhD

      Affiliations

    • Department of Epidemiology and Biostatistics, Case Western Reserve University School of Medicine, Cleveland, Ohio
  • ,
  • Daniel I. Simon, MD

      Affiliations

    • Harrington-McLaughlin Heart and Vascular Institute, University Hospitals Case Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio
  • ,
  • James C. Fang, MD

      Affiliations

    • Harrington-McLaughlin Heart and Vascular Institute, University Hospitals Case Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio

Received 31 January 2011; received in revised form 11 March 2011; accepted 11 March 2011. published online 25 May 2011.

The renin–angiotensin system is an important mediator of tumor progression and metastasis. A recent meta-analysis of randomized controlled trials reported an increased risk of cancer with angiotensin receptor blockers. It is unknown whether angiotensin-converting enzyme (ACE) inhibitors may have a similar effect. Our primary objective was to determine the effect of ACE inhibitors on cancer occurrence and cancer death. Our secondary objective was to determine the effect of ACE inhibitors on occurrence of gastrointestinal (GI) cancers given previous concerns of increased risk. Systematic searches of SCOPUS (covering MEDLINE, EMBASE, and other databases) and the Food and Drug Administration official web site were conducted for all randomized controlled trials of ACE inhibitors. Trials with ≥1 year of follow-up and enrolling a minimum of 100 patients were included. Fourteen trials reported cancer data in 61,774 patients. This included 10 trials of 59,004 patients providing information on cancer occurrence, 7 trials of 37,515 patients for cancer death, and 5 trials including 23,291 patients for GI cancer. ACE inhibitor therapy did not have an effect on occurrence of cancer (I2 0%, risk ratio [RR] 1.01, 95% confidence interval [CI] 0.95 to 1.07, p = 0.78), cancer death (I2 0%, RR 1.00, 95% CI 0.88 to 1.13, p = 0.95), or GI cancer (RR 1.09, 95% CI 0.88 to 1.35, p = 0.43). In conclusion, ACE inhibitors did not significantly increase or decrease occurrence of cancer or cancer death. There was also no significant difference in risk of GI cancer.

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 Dr. Sipahi received an educational grant (2004) and lecture honoraria from Pfizer (once, 2007), and lecture honoraria from AstraZeneca (once, 2008) and Ranbaxy (once, 2010). Dr. Debanne is a member of the data monitoring committee for Centocor Research & Development, Inc. Dr. Simon serves on advisory boards for Cordis/Johnson & Johnson, Daiichi-Sankyo, Medicines Company, Medtronic Vascular, Portola, and Schering-Plough, and has received lecture honoraria from Accumetrics, Cordis/Johnson & Johnson, Daiichi-Sankyo, Eli Lilly, Medicines Company, Sanofi-Aventis, and Schering-Plough. Dr. Fang serves on an advisory panel for Novartis and as a consultant for ARCA Biopharma, Inc.

PII: S0002-9149(11)01279-3

doi:10.1016/j.amjcard.2011.03.038

American Journal of Cardiology
Volume 108, Issue 2 , Pages 294-301, 15 July 2011