European Journal of Cancer
Volume 41, Issue 14 , Pages 2040-2059, September 2005

Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors

  • Sara Gandini

      Affiliations

    • Department of Epidemiology and Biostatistics, European Institute of Oncology IRCCS, Via Ripamonti 435, 20141 Milan, Italy
    • Corresponding Author InformationCorresponding author. Tel.: +39 02 57489819; fax: +39 02 57489922.
  • ,
  • Francesco Sera

      Affiliations

    • Molecular and Nutritional Epidemiology Unit, CSPO, Scientific Institute of Tuscany, Via di San Salvi 12, 50135 Florence, Italy
  • ,
  • Maria Sofia Cattaruzza

      Affiliations

    • Department of Public Health Sciences, University La Sapienza, Piazzale Aldo Moro 5, 00185 Rome, Italy
  • ,
  • Paolo Pasquini

      Affiliations

    • Laboratory of Clinical Epidemiology Istituto Dermopatico dell’Immaticolata (IDI) IRCCS, Via dei Monti di Creta 104, 00167 Rome, Italy
  • ,
  • Roberto Zanetti

      Affiliations

    • Piedmont Cancer Registry, CPO, Turin, Italy
  • ,
  • Cinzia Masini

      Affiliations

    • Istituto Dermopatico dell’Immaticolata (IDI) IRCCS, Via dei Monti di Creta 104, 00167 Rome, Italy
  • ,
  • Peter Boyle

      Affiliations

    • International Agency for Research on Cancer, Lyon, France
  • ,
  • Carmelo Francesco Melchi

      Affiliations

    • Istituto Dermopatico dell’Immaticolata (IDI) IRCCS, Via dei Monti di Creta 104, 00167 Rome, Italy

Received 11 February 2005; accepted 16 March 2005.

Abstract 

A systematic meta-analysis of observational studies of melanoma and family history, actinic damage and phenotypic factors was conducted as part of a comprehensive meta-analysis of all major risk factors for melanoma. Following a systematic literature search, relative risks were extracted from 60 studies published before September 2002. Fixed and random effects models were used to obtain pooled estimates for family history (RR=1.74, 1.41–2.14), skin type (I vs. IV: RR=2.09, 1.67–2.58), high density of freckles (RR=2.10, 1.80–2.45), skin colour (Fair vs. Dark: RR=2.06, 1.68–2.52), eye colour (Blue vs. Dark: RR=1.47, 1.28–1.69) and hair colour (Red vs. Dark: RR=3.64, 2.56–5.37), pre-malignant and skin cancer lesions (RR=4.28, 2.80–6.55) and actinic damage indicators (RR=2.02, 1.24–3.29). Sub-group analysis and meta-regression were carried out to explore sources of between-study variation and bias. Sensitivity analyses investigated reliability of results and publication bias. Latitude and adjustment for phenotype were two study characteristics that significantly influenced the estimates.

Keywords: Melanoma, Meta-analysis, Epidemiology, Review literature, Phenotype, Family history, Actinic damage

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PII: S0959-8049(05)00545-9

doi:10.1016/j.ejca.2005.03.034

European Journal of Cancer
Volume 41, Issue 14 , Pages 2040-2059, September 2005