CYP2D6 genotype predicts tamoxifen discontinuation and drug response: a secondary analysis of the KARISMA trial

被引:17
作者
He, W. [1 ,2 ,3 ,4 ]
Eriksson, M. [4 ]
Eliasson, E. [5 ,6 ]
Grassmann, F. [4 ,7 ]
Backlund, M. [4 ]
Gabrielson, M. [4 ]
Hammarstrom, M. [4 ]
Margolin, S. [8 ,9 ]
Thoren, L. [8 ,9 ]
Wengstrom, Y. [10 ]
Borgquist, S. [11 ,12 ,13 ,14 ]
Hall, P. [4 ,8 ]
Czene, K. [4 ]
机构
[1] Zhejiang Univ, Childrens Hosp, Chron Dis Res Inst, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Publ Hlth, Sch Med, Natl Clin Res Ctr Child Hlth, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Publ Hlth, Dept Nutr & Food Hyg, Hangzhou, Zhejiang, Peoples R China
[4] Karolinska Inst, Dept Med Epidemiol & Biostat, Nobels Vagen 12A, S-17177 Stockholm, Sweden
[5] Karolinska Inst, Dept Lab Med, Clin Pharmacol, Stockholm, Sweden
[6] Karolinska Univ Hosp, Stockholm, Sweden
[7] Univ Aberdeen, Inst Med Sci, Aberdeen, Scotland
[8] South Gen Hosp, Dept Oncol, Stockholm, Sweden
[9] Karolinska Inst, Dept Clin Sci & Educ Sodersjukhuset, Stockholm, Sweden
[10] Karolinska Univ Hosp, Dept Neurobiol Care Sci & Soc, Div Nursing & Theme Canc, Stockholm, Sweden
[11] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
[12] Aarhus Univ, Aarhus, Denmark
[13] Lund Univ, Dept Clin Sci Lund, Oncol, Lund, Sweden
[14] Skane Univ Hosp, Lund, Sweden
基金
瑞典研究理事会;
关键词
tamoxifen; treatment discontinuation; mammographic density; breast cancer; BREAST-CANCER CHEMOPREVENTION; QUALITY-OF-LIFE; CYTOCHROME-P450; 2D6; CLINICAL-OUTCOMES; AMERICAN SOCIETY; RISK REDUCTION; WOMEN; THERAPY; PHARMACOGENETICS; POLYMORPHISMS;
D O I
10.1016/j.annonc.2021.07.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Guidelines regarding whether tamoxifen should be prescribed based on women's cytochrome P450 2D6 (CYP2D6) genotypes are conflicting and have caused confusion. This study aims to investigate if CYP2D6 metabolizer status is associated with tamoxifen-related endocrine symptoms, tamoxifen discontinuation, and mammographic density change. Patients and methods: We used data from 1440 healthy women who participated the KARISMA dose determination trial. Endocrine symptoms were measured using a modified Functional Assessment of Cancer Therapy - Endocrine Symptoms (FACT-ES) questionnaire. Change in mammographic density was measured and used as a proxy for tamoxifen response. Participants were genotyped and categorized as poor, intermediate, normal, or ultrarapid CYP2D6 metabolizers. Results: The median endoxifen level per mg oral tamoxifen among poor, intermediate, normal and ultrarapid CYP2D6 metabolizers were 0.18 ng/ml, 0.38 ng/ml, 0.56 ng/ml and 0.67 ng/ml, respectively. Ultrarapid CYP2D6 metabolizers were more likely than other groups to report a clinically relevant change in cold sweats, hot flash, mood swings, being irritable, as well as the overall modified FACT-ES score, after taking tamoxifen. The 6-month tamoxifen discontinuation rates among poor, intermediate, normal, and ultrarapid CYP2D6 metabolizers were 25.7%, 23.6%, 28.6%, and 44.4%, respectively. Among those who continued and finished the 6-month tamoxifen intervention, the mean change in dense area among poor, intermediate, normal, and ultrarapid CYP2D6 metabolizers were -0.8 cm(2), -4.5 cm(2), -4.1 cm(2), and -8.0 cm(2) respectively. Conclusions: Poor CYP2D6 metabolizers are likely to experience an impaired response to tamoxifen, measured through mammographic density reduction. In contrast, ultrarapid CYP2D6 metabolizers are at risk for exaggerated response with pronounced adverse effects that may lead to treatment discontinuation.
引用
收藏
页码:1286 / 1293
页数:8
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