Cyclooxygenase-2 expression correlates with diminished survival in invasive breast cancer treated with mastectomy and radiotherapy

被引:34
|
作者
O'Connor, JK
Avent, J
Lee, RJ
Fischbach, J
Gaffney, DK
机构
[1] Univ Utah, Dept Radiat Oncol, Salt Lake City, UT 84132 USA
[2] Latter Day St Hosp, Dept Pathol, Salt Lake City, UT 84143 USA
[3] Latter Day St Hosp, Dept Radiat Med, Salt Lake City, UT 84143 USA
关键词
COX-2; breast cancer; radiotherapy;
D O I
10.1016/j.ijrobp.2003.08.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the relationship between cyclooxygenase-2 (COX-2) expression and pathologic features and outcome in invasive breast cancer. Methods and Materials: Formalin-fixed, paraffin-embedded tumor specimens from 23 women with invasive breast cancer were stained for COX-2 expression. All women underwent mastectomy and locoregional radiotherapy. The distribution (percentage of positive staining cells) and intensity of COX-2 expression within the tumor cells were compared with clinical factors, including stage, grade, lymph node involvement, and outcome. Results: For invasive breast cancer, the distribution and intensity of COX-2 tumor expression correlated significantly with diminished overall survival. The 5-year overall survival rate was 100% for patients with <75% of breast cancer cells expressing COX-2 compared with 49% for patients with >= 75% (p = 0.044). The 5-year overall survival rate was 100% for patients with COX-2 intensity <80 compared with 60% for patients with COX-2 intensity greater than or equal to80 (p = 0.018). The percentage and intensity of COX-2 expression also correlated significantly with disease-free survival. The percentage of cells expressing COX-2 was significantly greater in women <40 years old than in women >= 40 years old (81% vs. 59%, respectively, p = 0.04). Conclusion: Both the distribution and the intensity of COX-2 expression correlated significantly with disease-free and overall survival in patients with invasive breast cancer. Younger patients with invasive breast cancer may have a greater percentage of COX-2 expression in their tumors. (C) 2004 Elsevier Inc.
引用
收藏
页码:1034 / 1040
页数:7
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