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Does anti-EGFR therapy improve outcome in advanced colorectal cancer? A systematic review and meta-analysis

  • Claire L. Vale

      Affiliations

    • Medical Research Council Clinical Trials Unit, Aviation House, 125 Kingsway, London WC2B 6NH, UK
    • Corresponding Author InformationCorresponding author. Tel.: +44 0 20 76704723.
  • ,
  • Jayne F. Tierney

      Affiliations

    • Medical Research Council Clinical Trials Unit, Aviation House, 125 Kingsway, London WC2B 6NH, UK
  • ,
  • David Fisher

      Affiliations

    • Medical Research Council Clinical Trials Unit, Aviation House, 125 Kingsway, London WC2B 6NH, UK
  • ,
  • Richard A. Adams

      Affiliations

    • Clinical Senior Lecturer/Honorary Consultant in Oncology, Cardiff University and Velindre Cancer Centre, Cardiff, UK
  • ,
  • Richard Kaplan

      Affiliations

    • Medical Research Council Clinical Trials Unit, Aviation House, 125 Kingsway, London WC2B 6NH, UK
  • ,
  • Timothy S. Maughan

      Affiliations

    • Gray Institute for Radiation Oncology and Biology, University of Oxford, Oxford OX3 7DQ, UK
  • ,
  • Mahesh K.B. Parmar

      Affiliations

    • Medical Research Council Clinical Trials Unit, Aviation House, 125 Kingsway, London WC2B 6NH, UK
  • ,
  • Angela M. Meade

      Affiliations

    • Medical Research Council Clinical Trials Unit, Aviation House, 125 Kingsway, London WC2B 6NH, UK

Received 25 August 2011; received in revised form 1 November 2011; accepted 5 November 2011. published online 28 November 2011.
Corrected Proof

Abstract 

Background

Randomised controlled trials (RCTs) of anti-EGFR monoclonal antibodies (MAb) in patients with advanced colorectal cancer (aCRC) have reported conflicting results.

Methods

A systematic review of RCTs comparing standard treatments±anti-EGFR MAbs was conducted. Hazard ratios (HR) for progression-free (PFS) and overall survival (OS) were derived for patients with wild-type (WT) and mutant KRAS. Prespecified analyses were conducted for line of treatment, MAb used, chemotherapy regimen, and choice of fluouropyrimidine. Trials using bevacizumab on both arms were included in a sensitivity analysis.

Results

Fourteen eligible RCTs were identified, with results by KRAS status available for ten RCTs. For third line treatment, the effect of anti-EGFR MAbs depended on KRAS status (interaction p<0.00001), with a PFS benefit for patients with WT KRAS only (HR=0.43, 95% CI 0.35–0.52, p<0.00001). For first and second line treatment, the effect also appeared to depend on KRAS status (interaction p=0.0003), again with the PFS benefit only for patients with WT KRAS (HR=0.83, 95% CI 0.76–0.90, p<0.0001). Differences between trial results (heterogeneity p=0.02, I2=62%) were best explained by the fluouropyrimidine used, with PFS benefits confined to trials combining MAbs alongside 5FU-based chemotherapy (HR=0.77, 95% CI 0.70–0.85, p<0.00001). There was no evidence of a PFS benefit when MAbs were given with bevacizumab.

Conclusions

For aCRC patients with WT KRAS, there are clear benefits of anti-EGFR MAbs in the third line and in the first and second line, when used alongside infusional 5FU-based regimens. However, there is no benefit for patients with KRAS mutations.

Keywords: Colorectal cancer, Anti-EGFR therapy, Systematic review, Meta-analysis

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PII: S0305-7372(11)00241-6

doi:10.1016/j.ctrv.2011.11.002

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