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EZH2表达在接受新辅助放化疗的直肠癌患者中的预后作用。

The prognostic role of EZH2 expression in rectal cancer patients treated with neoadjuvant chemoradiotherapy.

作者信息

Meng Xiangjiao, Huang Zhaoqin, Wang Renben, Jiao Yuhong, Li Huijuan, Xu Xiaoqing, Feng Rui, Zhu Kunli, Jiang Shumei, Yan Hongjiang, Yu Jinming

机构信息

Department of Radiation Oncology of Shandong Cancer Hospital and Institute, No, 440 Jiyan Road, Jinan, Shandong 250117, China.

出版信息

Radiat Oncol. 2014 Aug 27;9:188. doi: 10.1186/1748-717X-9-188.

Abstract

BACKGROUND

Neoadjuvant chemoradiotherapy (nCRT) combined with surgery has been implemented as a standard treatment strategy in locally advanced rectal cancer (LARC). However, there is a wide spectrum of response to nCRT. The aim of this study was to determine whether enhancer of zeste homologue 2 (EZH2 ) expression could predict response to nCRT and outcomes for patients in LARC.

METHOD

The study examined the EZH2 expression in 112 biopsies by immohistochemistry. The associations between EZH2 and clinical characters were analyzed.

RESULTS

EZH2 expression in biopsy tissue was significantly related to increased tumor cell proliferation, as assessed by Ki-67 expression with a cutoff value of 37% (p <0.001). High EZH2 expression was correlated closely with low differentiation (p = 0.029), high CEA level (p = 0.041), T4 status (p = 0.011) and node metastasis (p =0.045). By univariate and multivariate analysis, we observed low EZH2 expression could reliably and independently predict the good response to nCRT ( p = 0.026 and p = 0.023) and down-staging ( p = 0.021 and p = 0.027). In univariate analysis, high EZH2 expression was significantly associated with poor 5-year disease-free survival (p = 0.025) and 5-year overall survival (p = 0.032). In multivariate analysis, EZH2 was a prognostic factor for 5-year DFS (HR = 2.287; 95% CI 1.137-4.602, p = 0.020) but not for 5-year OS (HR = 2.182; 95% CI 0.940-5.364, p = 0.069).

CONCLUSION

Our study revealed that low EZH2 expression in biopsy tissue might be a useful predictive factor of good tumor response to nCRT and longer 5-year DFS in patients with LARC. However this is a relatively small retrospective study, to further validate the role of EZH2 in rectal cancer, large consistent cohort studies are needed.

摘要

背景

新辅助放化疗(nCRT)联合手术已成为局部晚期直肠癌(LARC)的标准治疗策略。然而,对nCRT的反应存在广泛差异。本研究的目的是确定zeste同源物2增强子(EZH2)的表达是否可以预测LARC患者对nCRT的反应及预后。

方法

本研究通过免疫组织化学检测了112份活检组织中的EZH2表达。分析了EZH2与临床特征之间的关联。

结果

活检组织中EZH2的表达与肿瘤细胞增殖增加显著相关,以Ki-67表达评估,临界值为37%(p<0.001)。EZH2高表达与低分化(p=0.029)、高癌胚抗原(CEA)水平(p=0.041)、T4分期(p=0.011)和淋巴结转移(p=0.045)密切相关。通过单因素和多因素分析,我们观察到EZH2低表达可以可靠且独立地预测对nCRT的良好反应(p=0.026和p=0.023)以及降期(p=0.021和p=0.027)。在单因素分析中,EZH2高表达与5年无病生存率差(p=0.025)和5年总生存率差(p=0.032)显著相关。在多因素分析中,EZH2是5年无病生存的预后因素(风险比[HR]=2.287;95%置信区间[CI]1.137-4.602,p=0.020),但不是5年总生存的预后因素(HR=2.182;95%CI0.940-5.364,p=0.069)。

结论

我们的研究表明,活检组织中EZH2低表达可能是LARC患者肿瘤对nCRT反应良好及5年无病生存期更长的有用预测因素。然而,这是一项相对较小的回顾性研究,为进一步验证EZH2在直肠癌中的作用,需要开展大型一致性队列研究。

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