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CDX2表达与T分期相结合可改善结直肠癌的预后预测。

Combination of CDX2 expression and T stage improves prognostic prediction of colorectal cancer.

作者信息

Xu Weimin, Zhu Yilian, Shen Wei, Ding Wenjun, Wu Tingyu, Guo Yuegui, Chen Xiaobing, Zhou Mingxia, Chen Yingwei, Cui Long, Du Peng

机构信息

1 Department of Colorectal Surgery, Xin-Hua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

2 Department of Oncology, Henan Cancer Hospital, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

J Int Med Res. 2019 May;47(5):1829-1842. doi: 10.1177/0300060518819620. Epub 2019 Jan 7.

Abstract

OBJECTIVE

Prognostic prediction of colorectal cancer (CRC) remains challenging because of its heterogeneity. Aberrant expression of caudal-type homeobox transcription factor 2 (CDX2) is strongly correlated with the prognosis of CRC.

METHODS

Tissue samples of patients with CRC who underwent surgery in Xinhua Hospital (Shanghai, China) from January 2010 to January 2013 were collected. CDX2 expression was semiquantitatively evaluated via immunohistochemistry.

RESULTS

In total, 138 patients were enrolled in this study from a prospectively maintained institutional cancer database. The median follow-up duration was 57.5 months (interquartile range, 17.0-71.0 months). In the Cox proportional hazards model, low CDX2 expression combined with stage T4 CRC was significantly the worst prognostic factor for disease-free survival (hazard ratio = 7.020, 95% confidence interval = 3.922-12.564) and overall survival (hazard ratio = 5.176, 95% CI = 3.237-10.091). In the Kaplan-Meier survival analysis, patients with low CDX2 expression and stage T4 CRC showed significantly worse disease-free survival and overall survival than those with low CDX2 expression alone.

CONCLUSION

CDX2 expression combined with the T stage was more accurate for predicting the prognosis of CRC. Determining the prognosis of CRC using more than one variable is valuable in developing appropriate treatment and follow-up strategies.

摘要

目的

由于结直肠癌(CRC)具有异质性,其预后预测仍然具有挑战性。尾型同源框转录因子2(CDX2)的异常表达与CRC的预后密切相关。

方法

收集2010年1月至2013年1月在上海新华医院接受手术的CRC患者的组织样本。通过免疫组织化学对CDX2表达进行半定量评估。

结果

本研究共纳入138例患者,数据来自前瞻性维护的机构癌症数据库。中位随访时间为57.5个月(四分位间距,17.0 - 71.0个月)。在Cox比例风险模型中,低CDX2表达联合T4期CRC是无病生存(风险比 = 7.020,95%置信区间 = 3.922 - 12.564)和总生存(风险比 = 5.176,95%CI = 3.237 - 10.091)的显著最差预后因素。在Kaplan-Meier生存分析中,低CDX2表达且处于T4期CRC的患者无病生存和总生存均显著差于仅低CDX2表达的患者。

结论

CDX2表达联合T分期对预测CRC预后更准确。使用多个变量确定CRC的预后对于制定合适的治疗和随访策略具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/989a/6567745/cc8f7ef439a4/10.1177_0300060518819620-fig1.jpg

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