Racial differences in cyp3a4 genotype and survival among men treated on radiation therapy oncology group (rtog) 9202: A phase III randomized trial

被引:13
|
作者
Roach, Mack, III
De Silvio, Michelle
Rebbick, Timothy
Grignon, David
Rotman, Marvin
Wolkov, Harvey
Fisher, Barbara
Hanks, Gerald
Shipley, William U.
Pollack, Alan
Sandler, Howard
Watkins-Bruner, Deborah
机构
[1] Univ Calif San Francisco, Ctr Comprehens Canc, Dept Radiat Oncol, San Francisco, CA 94143 USA
[2] RTOG Statist Headquaters, Philadelphia, PA USA
[3] Univ Penn, Philadelphia, PA 19104 USA
[4] Wayne State Univ, Detroit, MI USA
[5] Suny Downstate Med Ctr, Brooklyn, NY 11203 USA
[6] Radiol Associates Sacramento, Sacramento, CA USA
[7] Univ Western Ontario, London, ON, Canada
[8] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[9] Massachusetts Gen Hosp, Boston, MA 02114 USA
[10] Univ Michigan, Ann Arbor, MI 48109 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 69卷 / 01期
关键词
prostate cancer; radiotherapy; race; genetic polymorphisms;
D O I
10.1016/j.ijrobp.2007.03.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Inherited genotypes may explain the inferior outcomes of African American (AA) men with prostate cancer. To understand how variation in CYP3A4 correlated with outcomes, a retrospective examination of the CYP3A4*1B genotype was performed on men treated with Radiation Therapy Oncology Group (RTOG) 92-02. Methods and Materials: From 1,514 cases, we evaluated 56 (28.4%) of 197 AA and 54 (4.3%) of 1,274 European American (EA) -patients. All patients received goserelin and flutamide for 2 months before and during RT (STAD-RT) +/- 24 months of goserelin (long-term androgen deprivation plus radiation [LTAD-RT]). Events studied included overall survival and biochemical progression using American Society for Therapeutic Radiology and Oncology consensus guidelines. Results: There were no differences in outcome in patients in with or without CYP3A4 data. There was an association between race and CYP3A4 polymorphisms with 75% of EAs having the Wild Type compared to only 25% of AA men (p <0.0001). There was no association between CYP3A4 classification or race and survival or progression. Conclusions: The samples analyzed support previously reported observations about the distribution of CYP3A4*1B genotype by race, but race was not associated with poorer outcome. However, patient numbers were limited, and selection bias cannot be completely ruled out. (c) 2007 Elsevier Inc.
引用
收藏
页码:79 / 87
页数:9
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