Nuclear Maspin expression is associated with response to adjuvant 5-fluorouracil based chemotherapy in patients with stage III colon cancer

被引:48
作者
Dietmaier, W
Bettstetter, M
Wild, PJ
Woenckhaus, M
Rümmele, P
Hartmann, A
Dechant, S
Blaszyk, H
Pauer, A
Klinkhammer-Schalke, M
Hofstädter, F
机构
[1] Univ Regensburg, Inst Pathol, Dept Pathol & Mol Diagnost, D-93053 Regensburg, Germany
[2] Univ Regensburg, Dept Surg, D-93053 Regensburg, Germany
[3] Univ Vermont, Coll Med, Dept Pathol, Burlington, VT 05405 USA
[4] Univ Regensburg, Tumor Registry, D-8400 Regensburg, Germany
关键词
colon cancer; Maspin; prediction; 5-flourouracil; chemotherapy;
D O I
10.1002/ijc.21620
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Maspin, a member of the Serpin protease inhibitor family, is over-expressed in poorly differentiated colorectal tumors and more frequently found in tumors with microsatellite instability. Immunohistochemical nuclear Maspin staining is predominantly seen in tumor cells at the invasion front of such cancers, suggesting that this molecule is associated with local tumor cell infiltration and aggressiveness. In a retrospective study, we studied nuclear Maspin expression as a potential prognostic tool in a total of 172 primary stage III colon cancers by immunohistochemistry. Of those 172 patients, 76 were treated by surgery only, and 96 patients received additional adjuvant 5-fluorouracil (5-FU) based chemotherapy. Nuclear Maspin expression was an independent adverse prognostic factor for overall survival in our patient cohort (hazard ratio 2.08; 95% CI, 1.13-3.81; p = 0.018). However, patients with primary tumors expressing Maspin in the nucleus showed a significant treatment benefit from 5-FU chemotherapy (hazard ratio 0.384; 95% CI, 0.188-0.784; p = 0.009) compared to adjuvantly treated patients whose tumors did not express this molecule. Nuclear Maspin expression is highly predictive of 5-FU chemotherapy response in patients with advanced stage colon cancer. Patients with negative immunhistochemical Maspin expression do not benefit from 5-FU treatment anti may be candidates for an alternative (non-5-FU based) adjuvant therapy regime. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:2247 / 2254
页数:8
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