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Pharmaceuticals (Basel). 2010 Apr 15;3(4):1122-1138. doi: 10.3390/ph3041122.

The Impact of CYP2D6 Genotyping on Tamoxifen Treatment.

Pharmaceuticals (Basel, Switzerland)

Roberta Ferraldeschi, William G Newman

Affiliations

  1. Department of Medical Oncology, Christie Hospital NHS Trust, Wilmslow Road, Manchester M20 4BX, UK. [email protected].
  2. Genetic Medicine, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Oxford Road, Manchester, M13 9WL, UK. [email protected].
  3. Genetic Medicine, St Mary's Hospital, Manchester Academic Health Sciences Centre (MAHSC), University of Manchester, Oxford Road, Manchester, M13 9WL, UK. [email protected].

PMID: 27713292 PMCID: PMC4034025 DOI: 10.3390/ph3041122

Abstract

Tamoxifen remains a cornerstone of treatment for patients with oestrogen-receptor-positive breast cancer. Tamoxifen efficacy depends on the biotransformation, predominantly via the cytochrome P450 2D6 (CYP2D6) isoform, to the active metabolite endoxifen. Both genetic and environmental (drug-induced) factors may alter CYP2D6 enzyme activity directly affecting the concentrations of active tamoxifen metabolites. Several studies suggest that germline genetic variants in

Keywords: CYP2D6 genotyping; breast cancer; tamoxifen

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