Laboratory for Pharmacogenetics, RIKEN Center for Genomic Medicine, Yokohama, Japan.
Pharmacogenet Genomics. 2010 Sep;20(9):565-8. doi: 10.1097/FPC.0b013e32833af231.
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.
我们之前报道了 282 例接受他莫昔芬单药治疗的日本乳腺癌患者的细胞色素 P450 2D6(CYP2D6)基因型与临床结局之间的显著相关性。尽管许多研究小组提供了证据表明 CYP2D6 基因型是他莫昔芬反应的最强预测因子之一,但结果仍然存在争议。我们假设伴随治疗是导致这些争议结果的原因之一。然后,我们研究了 167 例接受他莫昔芬联合治疗的乳腺癌患者,以评估伴随治疗对关联分析的影响,结果发现 CYP2D6 基因型与无复发生存期之间没有显著相关性(P=0.44,风险比:0.64,95%置信区间:0.20-1.99,在具有两个变异等位基因的患者与无变异等位基因的患者中)。当我们对淋巴结状态和肿瘤大小进行了两项亚组分析时,我们仅观察到在接受他莫昔芬单药治疗的患者中,CYP2D6 基因型与临床结局之间存在正相关。这项研究解释了报告结果之间差异的一部分。