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Irinotecan-induced toxicity pharmacogenetics: an umbrella review of systematic reviews and meta-analyses.
Campbell, J M; Stephenson, M D; Bateman, E; Peters, M D J; Keefe, D M; Bowen, J M.
Afiliação
  • Campbell JM; The Joanna Briggs Institute, Faculty of Health Science, University of Adelaide, Adelaide, South Australia, Australia.
  • Stephenson MD; The Joanna Briggs Institute, Faculty of Health Science, University of Adelaide, Adelaide, South Australia, Australia.
  • Bateman E; School of Medicine, Faculty of Health Science, University of Adelaide, Adelaide, South Australia, Australia.
  • Peters MD; The Joanna Briggs Institute, Faculty of Health Science, University of Adelaide, Adelaide, South Australia, Australia.
  • Keefe DM; School of Medicine, Faculty of Health Science, University of Adelaide, Adelaide, South Australia, Australia.
  • Bowen JM; School of Medicine, Faculty of Health Science, University of Adelaide, Adelaide, South Australia, Australia.
Pharmacogenomics J ; 17(1): 21-28, 2017 01.
Article em En | MEDLINE | ID: mdl-27503581
Irinotecan chemotherapy toxicities can be severe, and may result in treatment delay, morbidity and in some rare cases death. This systematic review of systematic reviews synthesises all meta-analyses on biomarkers for irinotecan toxicity across all genetic models for Asians, Caucasians, low dose, medium/high dose and regimens with and without fluorouracil. False-positive findings are a problem in pharmacogenetics, increasing the importance of systematic reviews. Four systematic reviews that investigated the effect of the polymorphisms UGT1A1*6 and/or*28 on neutropenia or diarrhoea toxicity were included. Both UGT1A1*6 and *28 were reliably demonstrated to be risk factors for irinotecan-induced neutropenia, with tests for both polymorphisms potentially being particularly useful in Asian cancer patients. UGT1A1*6 and *28 were also related to diarrhoea toxicity; however, at low doses of irinotecan there was evidence that UGT1A1*28 was not. In synthesising the best available evidence, this umbrella systematic review provides a novel reference for clinicians applying personalised medicine and identifies important research gaps.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacogenética / Camptotecina / Metanálise como Assunto / Glucuronosiltransferase / Polimorfismo de Nucleotídeo Único / Diarreia / Variantes Farmacogenômicos / Revisões Sistemáticas como Assunto / Neutropenia / Antineoplásicos Fitogênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Pharmacogenomics J Assunto da revista: BIOLOGIA MOLECULAR / FARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Farmacogenética / Camptotecina / Metanálise como Assunto / Glucuronosiltransferase / Polimorfismo de Nucleotídeo Único / Diarreia / Variantes Farmacogenômicos / Revisões Sistemáticas como Assunto / Neutropenia / Antineoplásicos Fitogênicos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Pharmacogenomics J Assunto da revista: BIOLOGIA MOLECULAR / FARMACOLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos