The Journal of Thoracic and Cardiovascular Surgery
Volume 136, Issue 4 , Pages 884-893, October 2008

Pexelizumab in ischemic heart disease: A systematic review and meta-analysis on 15,196 patients

  • L. Testa, MD, PhD, FEAPCI

      Affiliations

    • Institute of Cardiology, John Radcliffe Hospital, Oxford, United Kingdom
    • Corresponding Author InformationAddress for reprints: Luca Testa, MD, PhD, FEAPCI, Cardiology Ward, Level 2, John Radcliffe Hospital, Headley Way, Oxford, OX3 9DU, United Kingdom.
    • Specialist Cardiologist; Interventional Cardiology Fellow at John Radcliffe Hospital, Oxford, United Kingdom; Fellow of the European Association of Percutaneous Coronary Intervention; Research Fellow in Molecular Biology at Policlinico Gemelli, Institute of Cardiology, Rome, Italy.
  • ,
  • W.J. Van Gaal, MD, FRACP

      Affiliations

    • Institute of Cardiology, John Radcliffe Hospital, Oxford, United Kingdom
  • ,
  • R. Bhindi, MD, PhD, FESC

      Affiliations

    • Institute of Cardiology, John Radcliffe Hospital, Oxford, United Kingdom
  • ,
  • G.G.L. Biondi-Zoccai, MD

      Affiliations

    • Division of Cardiology, University of Turin, Turin, Italy
  • ,
  • A. Abbate, MD

      Affiliations

    • Department of Medicine, Virginia Commonwealth University, Richmond, Va
  • ,
  • P. Agostoni, MD

      Affiliations

    • Antwerp Cardiovascular Institute Middelheim, AZ Middelheim, Antwerp, Belgium
  • ,
  • I. Porto, MD

      Affiliations

    • Institute of Cardiology, Catholic University, Rome, Italy
  • ,
  • F. Andreotti, MD, FESC

      Affiliations

    • Institute of Cardiology, Catholic University, Rome, Italy
  • ,
  • F. Crea, MD, FESC, FACC

      Affiliations

    • Institute of Cardiology, Catholic University, Rome, Italy
  • ,
  • A.P. Banning, MD, FESC

      Affiliations

    • Institute of Cardiology, John Radcliffe Hospital, Oxford, United Kingdom

Received 10 October 2007; accepted 14 December 2007. published online 19 June 2008.

Object

Pexelizumab is a humanized monoclonal antibody inhibiting C5 complement. It has been postulated to improve outcomes in patients undergoing coronary artery bypass surgery and urgent reperfusion therapy for ST elevation myocardial infarction. We aimed at evaluating the risk/benefit profile of pexelizumab (bolus + infusion) versus placebo on top of current approaches in the management of patients with ST elevation myocardial infarction or undergoing coronary artery bypass.

Methods

We conducted a search of BioMedCentral, CENTRAL, mRCT, and PubMed without language restrictions (updated October 2007) for randomized controlled trials. Outcomes of interest were the risk of major adverse events (the composite of all-cause death, myocardial infarction, and thromboembolic stroke), the risk of single end points, and heart failure.

Results

Seven trials were included (15,196 patients: 7019 patients with ST elevation myocardial infarction and 8177 undergoing coronary bypass surgery). No benefit of adding pexelizumab was found in the overall analysis for major adverse events (OR 0.91 [0.76–1.09]; P = .29], death (OR 0.79 [0.61–1.03], P = .11], myocardial infarction (OR 1.04 [0.89–1.22]; P = .14), stroke (OR 0.95 [0.66–1.38]; P = .8), heart failure (OR1.0 [0.82–1.22]; P = .99), nor in the settings of patients with ST elevation myocardial infarction treated with mechanical or pharmacologic reperfusion therapy. Pexelizumab was associated with a 26% reduction of the risk of death in the setting of coronary artery bypass (OR 0.74 [0.58–0.94]; P = .01). The number needed to treat was 100.

Conclusion

Our data ruled out the hypothesis of any benefit of adding pexelizumab on top of currently available therapies for ST elevation myocardial infarction. However, pexelizumab reduces the risk of death in patients undergoing coronary artery bypass grafting.

Abbreviations and Acronyms: AMI, acute myocardial infarction, CABG, coronary artery bypass grafting, CHF, congestive heart failure, CI, confidence interval, MAC, membrane attack complex, MAE, major adverse event, MI, myocardial infarction, OR, odds ratio, QUOROM, Quality of Reporting of Meta-analyses, STEMI, ST elevation myocardial infarction

CTSNet classification: 16, 23, 25, 31

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 This study is part of a senior investigator project of the Center for Overview, Meta-analysis, and Evidence-based medicine Training (COMET), based in Oxford, United Kingdom (http://www.comet.gs).

PII: S0022-5223(08)00714-9

doi:10.1016/j.jtcvs.2007.12.062

The Journal of Thoracic and Cardiovascular Surgery
Volume 136, Issue 4 , Pages 884-893, October 2008