Association between CYP2D6*10 genotype and survival of breast cancer patients receiving tamoxifen treatment

被引:136
作者
Xu, Y. [2 ]
Sun, Y. [1 ]
Yao, L. [2 ]
Shi, L. [2 ]
Wu, Y. [2 ]
Ouyang, T. [2 ]
Li, J. [2 ]
Wang, T. [2 ]
Fan, Z. [2 ]
Fan, T. [2 ]
Lin, B. [2 ]
He, L. [3 ]
Li, P. [1 ]
Xie, Y. [2 ]
机构
[1] Peking Univ, Sch Oncol, Beijing Canc Hosp & Inst, Dept Tradit Chinese Med, Beijing 100036, Peoples R China
[2] Peking Univ, Sch Oncol, Beijing Canc Hosp & Inst, Breast Ctr, Beijing 100036, Peoples R China
[3] Peking Univ, Sch Oncol, Beijing Canc Hosp & Inst, Dept Biochem & Mol Biol, Beijing 100036, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; CYP2D6*10 genotype; survival; tamoxifen;
D O I
10.1093/annonc/mdn155
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Human cytochrome P450 2D6 (CYP2D6) genotype may affect the efficacy of tamoxifen treatment in Caucasian women with breast cancer. The most common polymorphism of CYP2D6 in Chinese women is variant 10 (188 C to T). Patients and methods: Tamoxifen and 4-hydroxytamoxifen (4OHtam) were measured in the serum of 37 women with breast cancer who were receiving tamoxifen treatment. The association between CYP2D6 *10 genotype and survival was determined in a cohort of 293 women with breast cancer who received tamoxifen (n = 152) or who did not (n = 141). Results: The serum 4OHtam concentrations were significantly lower in women with the CYP2D6 *10 homozygous variant T/T genotype than in those with the homozygous wild-type C/C genotype (P = 0.04). Among tamoxifen-treated women, women with the T/T genotype had a significantly worse disease-free survival (DFS) than those with the C/C or C/T genotype, and the T/T genotype remained an independent prognostic factor of DFS in multivariate analysis (hazard ratio = 4.7; 95% confidence interval = 1.1-20.0; P = 0.04). Among women who did not receive tamoxifen, there was no significant association between CYP2D6 *10 genotype and survival. Conclusion: In tamoxifen-treated patients, women with the CYP2D6 *10 T/T genotype have a lower 4OHtam level in the serum and a worse clinical outcome.
引用
收藏
页码:1423 / 1429
页数:7
相关论文
共 24 条
[1]   Anastrozole as an adjuvant endocrine treatment for postmenopausal patients with breast cancer: Emerging data [J].
Buzdar, AU ;
Cuzick, J .
CLINICAL CANCER RESEARCH, 2006, 12 (03) :1037S-1048S
[2]  
Dehal SS, 1997, CANCER RES, V57, P3402
[3]   Comprehensive evaluation of tamoxifen sequential biotransformation by the human cytochrome P450 system in vitro: Prominent roles for CYP3A and CYP2D6 [J].
Desta, Z ;
Ward, BA ;
Soukhova, NV ;
Flockhart, DA .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 310 (03) :1062-1075
[4]  
Garcia-Barceló M, 2000, CLIN CHEM, V46, P18
[5]   Pharmacogenetics of tamoxifen biotransformation is associated with clinical outcomes of efficacy and hot flashes [J].
Goetz, MP ;
Rae, JM ;
Suman, VJ ;
Safgren, SL ;
Ames, MM ;
Visscher, DW ;
Reynolds, C ;
Couch, FJ ;
Lingle, WL ;
Flockhart, DA ;
Desta, Z ;
Perez, EA ;
Ingle, JN .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (36) :9312-9318
[6]  
Hersberger M, 2000, CLIN CHEM, V46, P1072
[7]  
Ji L, 2002, CLIN CHEM, V48, P983
[8]   CYP2D6 genotype, antidepressant use, and tamoxifen metabolism during adjuvant breast cancer treatment [J].
Jin, Y ;
Desta, Z ;
Stearns, V ;
Ward, B ;
Ho, H ;
Lee, KH ;
Skaar, T ;
Storniolo, AM ;
Li, L ;
Araba, A ;
Blanchard, R ;
Nguyen, A ;
Ullmer, L ;
Hayden, J ;
Lemler, S ;
Weinshilboum, RM ;
Rae, JM ;
Hayes, DF ;
Flockhart, DA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (01) :30-39
[9]  
JOHANSSON I, 1994, MOL PHARMACOL, V46, P452
[10]   On-line high-performance liquid chromatographic electrospray ionization mass spectrometric method for the study of tamoxifen metabolism [J].
Jones, RM ;
Yuan, ZX ;
Lamb, JH ;
Lim, CK .
JOURNAL OF CHROMATOGRAPHY A, 1996, 722 (1-2) :249-255