抄録
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.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 565-568 |
| ページ数 | 4 |
| ジャーナル | Pharmacogenetics and Genomics |
| 巻 | 20 |
| 号 | 9 |
| DOI | |
| 出版ステータス | 出版済み - 09-2010 |
| 外部発表 | はい |
UN SDG
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All Science Journal Classification (ASJC) codes
- 遺伝学(臨床)
- 薬理学、毒性学および薬学一般
- 遺伝学
- 分子医療
- 分子生物学
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