Pharmacogenetic testing affects choice of therapy among women considering tamoxifen treatment
- PMID: 21970596
- PMCID: PMC3239226
- DOI: 10.1186/gm280
Pharmacogenetic testing affects choice of therapy among women considering tamoxifen treatment
Abstract
Background: Pharmacogenetic testing holds major promise in allowing physicians to tailor therapy to patients based on genotype. However, there is little data on the impact of pharmacogenetic test results on patient and clinician choice of therapy. CYP2D6 testing among tamoxifen users offers a potential test case of the use of pharmacogenetic testing in the clinic. We evaluated the effect of CYP2D6 testing in clinical practice to determine whether genotype results affected choice of hormone therapy in a prospective cohort study.
Methods: Women planning to take or currently taking tamoxifen were considered eligible. Participants were enrolled in an informational session that reviewed the results of studies of CYP2D6 genotype on breast cancer recurrence. CYP2D6 genotyping was offered to participants using the AmpliChip CYP450 Test. Women were classified as either poor, intermediate, extensive or ultra-rapid metabolizers. Results were provided to clinicians without specific treatment recommendations. Follow-up was performed with a structured phone interview 3 to 6 months after testing to evaluate changes in medication.
Results: A total of 245 women were tested and 235 completed the follow-up survey. Six of 13 (46%) women classified as poor metabolizers reported changing treatment compared with 11 of 218 (5%) classified as intermediate, extensive or ultra-rapid metabolizers (P < 0.001). There was no difference in treatment choices between women classified as intermediate and extensive metabolizers. In multi-variate models that adjusted for age, race/ethnicity, educational status, method of referral into the study, prior knowledge of CYP2D6 testing, the patients' CYP2D6 genotype was the only significant factor that predicted a change in therapy (odds ratio 22.8; 95% confidence interval 5.2 to 98.8). Genetic testing did not affect use of co-medications that interact with CYP2D6.
Conclusions: CYP2D6 genotype testing led to changes in therapy among poor metabolizers, even in the absence of definitive data that an alternative medicine improved outcomes. Pharmacogenetic testing can affect choice of therapy, even in the absence of definitive data on clinical impact.
Similar articles
-
Tamoxifen Therapy and CYP2D6 Genotype.2014 Oct 7 [updated 2019 May 1]. In: Pratt VM, Scott SA, Pirmohamed M, Esquivel B, Kattman BL, Malheiro AJ, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012–. 2014 Oct 7 [updated 2019 May 1]. In: Pratt VM, Scott SA, Pirmohamed M, Esquivel B, Kattman BL, Malheiro AJ, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012–. PMID: 28520357 Free Books & Documents. Review.
-
Association between CYP2D6 polymorphisms and outcomes among women with early stage breast cancer treated with tamoxifen.JAMA. 2009 Oct 7;302(13):1429-36. doi: 10.1001/jama.2009.1420. JAMA. 2009. PMID: 19809024 Free PMC article.
-
The AmpliChip CYP450 genotyping test: Integrating a new clinical tool.Mol Diagn Ther. 2006;10(3):135-51. doi: 10.1007/BF03256453. Mol Diagn Ther. 2006. PMID: 16771600 Review.
-
Association between CYP2D6 genotype and tamoxifen-induced hot flashes in a prospective cohort.Breast Cancer Res Treat. 2009 Oct;117(3):571-5. doi: 10.1007/s10549-009-0309-1. Epub 2009 Jan 20. Breast Cancer Res Treat. 2009. PMID: 19153830 Free PMC article. Clinical Trial.
-
CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the breast international group 1-98 trial.J Natl Cancer Inst. 2012 Mar 21;104(6):441-51. doi: 10.1093/jnci/djs125. Epub 2012 Mar 6. J Natl Cancer Inst. 2012. PMID: 22395644 Free PMC article. Clinical Trial.
Cited by
-
CYP2D6 genotyping and use of antidepressants in breast cancer patients: test development for clinical application.Metab Brain Dis. 2012 Sep;27(3):319-26. doi: 10.1007/s11011-012-9312-z. Epub 2012 May 26. Metab Brain Dis. 2012. PMID: 22638694 Free PMC article.
-
Estimation of tamoxifen metabolite concentrations in the blood of breast cancer patients through CYP2D6 genotype activity score.Breast Cancer Res Treat. 2012 Jun;133(2):677-83. doi: 10.1007/s10549-012-1963-2. Breast Cancer Res Treat. 2012. PMID: 22294487 Free PMC article.
-
Targeted variant prevalence of FBXW7 gene mutation in colorectal carcinoma propagation. The first systematic review and meta-analysis.Heliyon. 2024 May 22;10(11):e31471. doi: 10.1016/j.heliyon.2024.e31471. eCollection 2024 Jun 15. Heliyon. 2024. PMID: 38845996 Free PMC article.
-
CYP2D6 genotype and tamoxifen activity: understanding interstudy variability in methodological quality.Clin Pharmacol Ther. 2013 Aug;94(2):185-7. doi: 10.1038/clpt.2013.66. Clin Pharmacol Ther. 2013. PMID: 23872831 Free PMC article. No abstract available.
-
Personalized participatory medicine: sharing knowledge and uncertainty.Genome Med. 2011 Oct 27;3(10):69. doi: 10.1186/gm285. Genome Med. 2011. PMID: 22035871 Free PMC article.
References
-
- Group EBCTC. Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet. 2005;365:1687–1717. - PubMed