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Meta-analyses of randomised clinical trials in oncology

Journal

LANCET ONCOLOGY
Volume 2, Issue 8, Pages 475-482

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S1470-2045(01)00453-3

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Funding

  1. l'Association pour la Recherche sur le Cancer [5137]
  2. Programme Hospitalier de Recherche Clinique [AOM 98 083]

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A meta-analysis is a quantitative synthesis of randomised clinical trials, used to evaluate moderate treatment effects in oncology. It is complementary to large-scale trials. We describes the principles, methods, and limits of meta-analyses. The gold standard for a meta-analysis is to obtain individual patient data directly from each principal investigator, but this is time-consuming and costly. The main steps of a meta-analysis using individual patient data are described. Multidisciplinary collaboration is needed for clinical insight and critical review of the data and results. Meta-analysis should include an evaluation of the trial quality, a quantification of the overall treatment effect, a study of the variations seen in this effect between trials, and pre-planned exploratory analyses to identify groups of patients who may benefit more from the treatment. Statistical methods are explained using real working examples. Since literature-based meta-analysis can lead to seriously biased assessments, meta-analyses of individual patient data should be undertaken systematically when long-term follow-up is needed, when a detailed analysis is important, or when the literature-based meta-analyses are not in agreement. The main factors which influence the quality of a meta-analysis are discussed.

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