Microsatellite instability did not predict individual survival in sporadic stage II and III rectal cancer patients

被引:19
|
作者
Meng, Wen-Jian
Sun, Xiao-Feng
Tian, Chao
Wang, Ling
Yu, Yong-Yang
Zhou, Bing
Gu, Jun
Xia, Qing-Jie
Li, Yuan
Wang, Rong
Zheng, Xue-Lian
Zhou, Zong-Guang
机构
[1] Sichuan Univ, W China Hosp, Dept Surg Gastroenterol, Chengdu 610064, Peoples R China
[2] Sichuan Univ, W China Hosp, Div Digest Dis & Organ Microcirculat, Chengdu, Peoples R China
[3] Sichuan Univ, W China Hosp, Ophthalmol Surg Lab, Chengdu, Peoples R China
[4] Sichuan Univ, W China Hosp, Natl Key Lab Biotheraphy, Chengdu, Peoples R China
[5] Linkoping Univ, Dept Oncol, Linkoping, Sweden
关键词
microsatellite instability; prognosis; sporadic rectal cancer; tumor stage;
D O I
10.1159/000111107
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Tumors with high-frequency microsatellite instability (MSI-H) have unique biological behavior and the predictive role of microsatellite instability (MSI) status on survival of colorectal cancer is still debated. The prognostic significance of MSI status in sporadic stage II and III rectal cancer patients needs to be more precisely defined. So we investigated the relationship between MSI status and clinicopathological features and prognosis in these patients. Methods: DNAs from fresh-frozen paired samples of tumors and corresponding normal tissue from 128 stage II and III rectal cancer patients were analyzed for MSI by PCR amplification using markers recommended by a National Cancer Institute workshop on MSI. To assess prognostic significance, Cox proportional hazards modeling was used. Results: Twelve (9.3%) tumors in our study were MSI-H, 28 (21.9%) were low-frequency MSI (MSI-L) and 88 (68.8%) were microsatellite stable (MSS). Most of the MSI-H tumors compared with MSI-L and MSS tumors were found in female patients (p = 0.031), had mucinous histology (p = 0.023), high grade of differentiation (p = 0.002) and high level of preoperative serum carcinoembryonic antigen (p = 0.005). Rectal cancer patients with MSI-H did not show a better clinical outcome than those with MSI-L/MSS, neither in all cases (p = 0.986) nor in stage II and stage III disease analyzed separately (p = 0.705 and p = 0.664, respectively). Conclusions: Data provided here demonstrated there was high incidence of MSI-H and MSI was not a prognostic factor in sporadic stage II and III rectal cancers from the Chinese Han population included in this study. Tumor stage is more suitable than MSI status for prediction of individual survival in sporadic stage II and III rectal cancer patients. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:82 / 88
页数:7
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