Literature DB >> 31559573

Cost-effectiveness Analysis of CYP2D6*10 Pharmacogenetic Testing to Guide the Adjuvant Endocrine Therapy for Postmenopausal Women with Estrogen Receptor Positive Early Breast Cancer in China.

Xiaoxia Wei1, Hong Sun1, Jie Zhuang1, Xiuhua Weng2, Bin Zheng3, Qiwang Lin4, Guifeng Zhang5, Jiaqin Cai6.   

Abstract

BACKGROUND: A CYP2D6 gene polymorphism is related to the effect of tamoxifen treatment in patient with estrogen-receptor positive (ER) positive breast cancer and CYP2D6*10 T/T can lead to a poor prognosis in Asian patients. Although one-off pharmacogenetic testing may optimize adjuvant endocrine therapy, testing prior to tamoxifen initiation incurs additional costs. AIM: We conducted a study to assess the cost-effectiveness of CYP2D6*10 pharmacogenetic testing to guide the adjuvant endocrine therapy compared with tamoxifen without CYP2D6*10 testing in China.
METHODS: A semi-Markov model was developed to evaluate costs and health outcomes represented as quality adjusted life year (QALY) gained. Input data were obtained from the public literature. The results were expressed as incremental cost per QALY gained. A one-way deterministic sensitivity analysis explored the impact of uncertainty in the model parameters on results, and probabilistic uncertainty was assessed through a Monte Carlo probabilistic sensitivity analysis.
RESULTS: In the base-case analysis, in the CYP2D6*10 testing and alternative adjuvant endocrine therapy group, the incremental total cost was US$17,966.95 and the incremental QALY was 3.582. Thus, the incremental cost-effectiveness ratio was US$5015.693 per QALY gained. Compared with a willingness-to-pay threshold of US$26,508/QALY in China, the CYP2D6*10 testing is the dominant strategy in postmenopausal women with ER-positive breast cancer in China, and the increased cost of genetic testing was completely worthwhile. The sensitivity analyses showed that the model we built was quite stable.
CONCLUSION: From the perspective of the Chinese healthcare system, CYP2D6*10 pharmacogenetic testing was cost effective for postmenopausal women with ER-positive early breast cancer.

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Year:  2020        PMID: 31559573     DOI: 10.1007/s40261-019-00842-0

Source DB:  PubMed          Journal:  Clin Drug Investig        ISSN: 1173-2563            Impact factor:   2.859


  24 in total

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2.  One step at a time: CYP2D6 guided tamoxifen treatment awaits convincing evidence of clinical validity.

Authors:  Daniel L Hertz; James M Rae
Journal:  Pharmacogenomics       Date:  2016-06-01       Impact factor: 2.533

3.  A Simulation Study to Compare the Treatment Effect of Tamoxifen by CYP2D6 Genotypes and Third-Generation Aromatase Inhibitors.

Authors:  Gwan Cheol Park; Jin-A Jung; Kyun-Seop Bae; Hyeong-Seok Lim
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5.  Adjuvant tamoxifen and exemestane in early breast cancer (TEAM): a randomised phase 3 trial.

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6.  Aromatase inhibitors versus tamoxifen in early breast cancer: patient-level meta-analysis of the randomised trials.

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7.  National Prociency Testing Result of CYP2D6*10 Genotyping for Adjuvant Tamoxifen Therapy in China.

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9.  The effect of CYP2D6 *10 polymorphism on adjuvant tamoxifen in Asian breast cancer patients: a meta-analysis.

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2.  The Role of CYP2D6 Polymorphisms in Determining Response to Tamoxifen in Metastatic Breast Cancer Patients: Review and Egyptian Experience.

Authors:  Ibrahim Malash; Osman Mansour; Sabry Shaarawy; Mona S Abdellateif; Anan Omar; Rabab Gaafer; Abdel-Rhaman N Zekri; Ola S Ahmed; Abeer Bahnassy
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Review 3.  A Review of the Important Role of CYP2D6 in Pharmacogenomics.

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  3 in total

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