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切除修复交叉互补基因 1 和胸苷酸合成酶在接受 FOLFOX 化疗的结直肠癌患者中的预后和预测作用:一项免疫组织化学研究。

Prognostic and Predictive Role of Excision Repair Cross-complementation Group 1 and Thymidylate Synthase in Colorectal Carcinoma Patients Received FOLFOX Chemotherapy: An Immunohistochemical Study.

机构信息

Pathology Department.

Faculty of Medicine, Assiut University.

出版信息

Appl Immunohistochem Mol Morphol. 2020 Nov/Dec;28(10):741-747. doi: 10.1097/PAI.0000000000000841.

Abstract

BACKGROUND AND STUDY AIMS

We aim to determine the frequency of thymidylate synthase (TS) and excision repair cross-complementation group 1 (ERCC-1) immunohistochemical (IHC) expression and its relationship with clinicopathologic variables in colorectal carcinoma (CRC) patients. In addition, we aim to assess the correlation between TS and ERCC-1 expression and the response of these cases to oxaliplatin and 5-fluorouracil chemotherapy (FOLFOX).

PATIENTS AND METHODS

Fifty-one CRC patients were prepared for IHC analysis of ERCC-1 and TS protein expression. All patients received oxaliplatin and 5-fluorouracil combined chemotherapy (FOLFOX) and were followed up for 24 months.

RESULTS

The data analysis showed that high ERCC-1 and TS expression was significantly associated with early treatment failure (P=0.020 and 0.000). In contrast, TS immunoexpression affects the disease-free survival rate (P=0.010). The presence of deep tumor invasion, distant metastasis, lymph node metastasis, and high Dukes' classification were significantly statistically associated with early treatment failure (P=0.001, 0.000, 0.041, and 0.015, respectively).

CONCLUSIONS

Our results showed that both ERCC-1 and TS are predictive factors for early treatment failure in CRC patients. TS protein is a prognostic factor for disease-free survival rates. This supports the theory that both ERCC-1 and TS can be used to improve chemotherapeutic outcomes in CRC patients. High expression of TS and ERCC-1 helps in the identification of cases that will get fewer benefits from FOLFOX chemotherapy. As an innovative strategy, in these cases, we can use alternative chemotherapeutic regimens or add an extra agent. In addition, Dukes' classification and lymph node metastasis are predictive factors for early treatment failure. Thus, all those values can be used to predict CRC patients with bad prognosis and those who will get fewer benefits from FOLFOX.

摘要

背景和研究目的

我们旨在确定胸苷酸合成酶(TS)和切除修复交叉互补组 1(ERCC-1)免疫组织化学(IHC)表达的频率及其与结直肠癌(CRC)患者临床病理变量的关系。此外,我们旨在评估 TS 和 ERCC-1 表达之间的相关性以及这些病例对奥沙利铂和 5-氟尿嘧啶化疗(FOLFOX)的反应。

患者和方法

对 51 例 CRC 患者进行 ERCC-1 和 TS 蛋白表达的 IHC 分析。所有患者均接受奥沙利铂和 5-氟尿嘧啶联合化疗(FOLFOX),并随访 24 个月。

结果

数据分析表明,高 ERCC-1 和 TS 表达与早期治疗失败显著相关(P=0.020 和 0.000)。相反,TS 免疫表达影响无病生存率(P=0.010)。肿瘤浸润深度、远处转移、淋巴结转移和 Dukes 分类较高均与早期治疗失败显著相关(P=0.001、0.000、0.041 和 0.015)。

结论

我们的结果表明,ERCC-1 和 TS 均为 CRC 患者早期治疗失败的预测因素。TS 蛋白是无病生存率的预后因素。这支持了 ERCC-1 和 TS 都可用于改善 CRC 患者化疗效果的理论。TS 和 ERCC-1 高表达有助于识别从 FOLFOX 化疗中获益较少的病例。作为一种创新策略,在这些情况下,我们可以使用替代化疗方案或添加额外的药物。此外,Dukes 分类和淋巴结转移是早期治疗失败的预测因素。因此,所有这些值都可用于预测预后不良的 CRC 患者和从 FOLFOX 中获益较少的患者。

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