Cytochrome P450 2D6 and homeobox 13/interleukin-17B receptor: Combining inherited and tumor gene markers for prediction of tamoxifen resistance

被引:18
作者
Goetz, Matthew P. [1 ,4 ]
Suman, Vera J. [2 ]
Couch, FergusJ. [3 ]
Ames, Matthew M. [4 ]
Rae, James M. [5 ]
Erlander, Mark G. [6 ]
Ma, Xiao-Jun [6 ]
Sgroi, Dennis C. [7 ]
Reynolds, Carol A. [3 ]
Lingle, Wilma L. [3 ]
Weinshilboum, Richard M. [4 ]
Flockhart, David A. [8 ]
Desta, Zeruesenay [8 ]
Perez, Edith A. [9 ]
Ingle, James N. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Oncol, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Biostat, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Dept Pathol, Rochester, MN 55905 USA
[4] Mayo Clin, Coll Med, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[5] Univ Michigan, Sch Med, Dept Med, Div Hematol Oncol, Ann Arbor, MI 48104 USA
[6] AviaraDx, San Diego, CA USA
[7] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Pathol,Mol Pathol Res Unit, Boston, MA 02115 USA
[8] Indiana Univ, Dept Med, Div Clin Pharmacol, Indianapolis, IN USA
[9] Mayo Clin, Dept Med, Div Hematol & Oncol, Jacksonville, FL 32224 USA
关键词
D O I
10.1158/1078-0432.CCR-08-0619
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: Genetic variation in cytochrome P450 2D6 (CYP2D6) and the gene expression ratio of the homeobox 13 (HOXB13) to interleukin-17B receptor (IL17BR) are associated with tamoxifen resistance. We sought to determine the combined effect of inherited (CYP2D6) and somatic (HOXB13/IL17BR) gene variation in tamoxifen-treated breast cancer. Experimental Design: Retrospective analysis of women with node-negative breast cancer randomized to receive 5 years of tamoxifen (North Central Cancer Treatment Group 89-30-52). CYP2D6 metabolism (extensive or decreased) was based on CYP2D6*4 genotype and presence/absence of a CYP2D6 inhibitor. Reverse transcription-PCR profiles for HOXB13 and IL17BR and the cut point separating patients into high- and low-risk categories according to disease-free survival (DFS) were used. A risk factor (CYP2D6:HOXB13/IL17BR) representing the four categories of combining CYP2D6 metabolism (extensive or decreased) and HOXB13/IL17BR (low or high) was created. The association between CYP2D6:HOXB13/IL17BR and DFS and overall survival (OS) was assessed using the log-rank test and proportional hazards modeling. Results: CYP2D6 metabolism and HOXB13/IL17BR gene ratio was available in 110 of 160 (69%) patients. The combined CYP2D6:HOXB13/IL17BR risk factor was significantly associated with DFS (log-rank P = 0.004) and OS (P = 0.009). Relative to women with extensive CYP2D6 metabolism and low HOXB13/IL17BR, those with either decreased metabolism or a high HOXB13/IL17BR ratio had significantly worse CS (adjusted hazard ratio, 2.41; 95% confidence interval, 1.08-5.37; P = 0.031), whereas women with both decreased metabolism and high HOXB13/IL17BR ratio had the shortest survival (adjusted hazard ratio, 3.15; 95% Cl, 1.17-8.52; P = 0.024). Conclusions: An index composed of inherited (CYP2D6) and tumor (HOXB13/IL17BR) gene variation identifies patients with varying degrees of resistance to tamoxifen.
引用
收藏
页码:5864 / 5868
页数:5
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