Lessons for pharmacogenomics studies: association study between CYP2D6 genotype and tamoxifen response

被引:38
作者
Kiyotani, Kazuma [2 ]
Mushiroda, Taisei [2 ]
Hosono, Naoya [3 ]
Tsunoda, Tatsuhiko [4 ]
Kubo, Michiaki [3 ]
Aki, Fuminori
Okazaki, Yutaka
Hirata, Koichi
Takatsuka, Yuichi
Okazaki, Minoru [5 ]
Ohsumi, Shozo [6 ]
Yamakawa, Takashi [7 ]
Sasa, Mitsunori [8 ]
Nakamura, Yusuke [1 ,2 ]
Zembutsu, Hitoshi
机构
[1] Univ Tokyo, Mol Med Lab, Ctr Human Genome, Inst Med Sci,Minato Ku, Tokyo 1088639, Japan
[2] RIKEN, Ctr Genom Med, Lab Pharmacogenet, Yokohama, Kanagawa, Japan
[3] RIKEN, Ctr Genom Med, Lab Genotyping Dev, Yokohama, Kanagawa, Japan
[4] RIKEN, Ctr Genom Med, Lab Med Informat, Yokohama, Kanagawa, Japan
[5] Sapporo Breast Surg Clin, Dept Surg, Sapporo, Hokkaido, Japan
[6] Shikoku Canc Ctr, Dept Breast Oncol, Shikoku, Ehime, Japan
[7] Yamakawa Breast Clin, Dept Surg, Kochi, Japan
[8] Tokushima Breast Care Clin, Dept Surg, Tokushima, Japan
关键词
breast cancer; chemotherapy; concomitant treatment; CYP2D6; endoxifen; monotherapy; P450; 2D6; tamoxifen; CLINICAL-OUTCOMES; POLYMORPHISMS; SURVIVAL; CYP2D6-ASTERISK-10; RECURRENCE; THERAPY;
D O I
10.1097/FPC.0b013e32833af231
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We earlier reported a significant association between the cytochrome P450 2D6 (CYP2D6) genotype and the clinical outcome in 282 Japanese breast cancer patients receiving tamoxifen monotherapy. Although many research groups have provided evidence indicating the CYP2D6 genotype as one of the strongest predictors of tamoxifen response, the results still remain controversial. We hypothesized that concomitant treatment was one of the causes of these controversial results. We then studied 167 breast cancer patients who received tamoxifen-combined therapy to evaluate the effects of concomitant treatment on the association analysis and observed no significant association between CYP2D6 genotype and recurrence-free survival (P = 0.44, hazard ratio: 0.64, 95% confidential interval: 0.20-1.99 in patients with two variant alleles vs. patients without a variant allele). When we carried out two subgroup analyses for nodal status and tumor size, we observed a positive association between the CYP2D6 genotype and the clinical outcome only in patients who received tamoxifen monotherapy. This study explained a part of the discrepancies among the reported results. Pharmacogenetics and Genomics 20: 565-568 (C) 2010 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:565 / 568
页数:4
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