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KRAS野生型转移性结直肠癌中EGFR蛋白表达是西妥昔单抗治疗的另一个阴性预测因子。

EGFR Protein Expression in KRAS Wild-Type Metastatic Colorectal Cancer Is Another Negative Predictive Factor of the Cetuximab Therapy.

作者信息

Uhlyarik Andrea, Piurko Violetta, Papai Zsuzsanna, Raso Erzsebet, Lahm Erika, Kiss Edina, Sikter Marta, Vachaja Jozsef, Kenessey Istvan, Timar Jozsef

机构信息

Department of Oncology, Medical Center, Hungarian Defence Forces, 1065 Budapest, Hungary.

2nd Department of Pathology, Semmelweis University, 1091 Budapest, Hungary.

出版信息

Cancers (Basel). 2020 Mar 6;12(3):614. doi: 10.3390/cancers12030614.

Abstract

The selection of colorectal cancer patients for anti-epidermal growth factor receptor (EGFR) antibody therapy is based on the determination of their RAS mutation status-a strongly negative predictive factor-since the protein target, EGFR, is not a reliable predictor of therapeutic response. In this study, we revisited the EGFR protein issue using a cohort of 90 patients with KRAS exon2 wild-type colorectal cancer who have been treated with cetuximab therapy. Twenty-nine of these patients had metastatic tissue available for analysis. The level of EGFR protein expression in the patients was determined by immunohistochemistry and evaluated by H-score (HS) methodology. Progression-free survival (PFS) and overall survival (OS) of the patients were determined according to the EGFR-HS ranges of both the primary and metastatic tissues using Kaplan-Meyer statistics. In the case of primary tumors, EGFR scores lower than HS = 200 were associated with significantly longer OS. In the case of metastatic tissues, all levels lower than the EGFR-HS range chosen were associated with significantly longer OS. These results are explained by the fact that metastatic tissues rarely maintained the expression levels of the primary tumors. On the other hand, high EGFR expression levels in either primary tumors or metastatic tissues were associated with multiple metastatic disease. This suggests a negative prognostic role of EGFR expression. However, in a multivariate analysis, one-sidedness remained a strong independent predictive factor of survival. Previous studies demonstrated that the EGFR expression level depends on sidedness. Therefore, a subgroup analysis of the left- and right-sided cases was performed on both primary and metastatic tissues. In the case of metastic tissues, an analysis confirmed a better OS in low EGFR protein-expressing cases than in high EGFR protein-expressing cases. Collectively, these data suggest that EGFR protein expression is another negative predictive factor of the efficacy of cetuximab therapy of KRAS exon2 wild-type colorectal cancer.

摘要

结直肠癌患者抗表皮生长因子受体(EGFR)抗体治疗的选择基于其RAS突变状态的判定——这是一个强有力的阴性预测因子——因为蛋白靶点EGFR并非治疗反应的可靠预测指标。在本研究中,我们使用一组接受西妥昔单抗治疗的90例KRAS外显子2野生型结直肠癌患者重新审视了EGFR蛋白问题。其中29例患者有可用于分析的转移组织。通过免疫组织化学测定患者的EGFR蛋白表达水平,并采用H评分(HS)方法进行评估。使用Kaplan - Meyer统计方法根据原发组织和转移组织的EGFR - HS范围确定患者的无进展生存期(PFS)和总生存期(OS)。对于原发肿瘤,EGFR评分低于HS = 200与显著更长的OS相关。对于转移组织,所有低于所选EGFR - HS范围的水平都与显著更长的OS相关。这些结果可以通过转移组织很少维持原发肿瘤的表达水平这一事实来解释。另一方面,原发肿瘤或转移组织中EGFR高表达水平与多发转移疾病相关。这表明EGFR表达具有负面预后作用。然而,在多变量分析中,肿瘤部位仍然是生存的一个强有力的独立预测因子。先前的研究表明EGFR表达水平取决于肿瘤部位。因此,对原发组织和转移组织的左右侧病例进行了亚组分析。对于转移组织,分析证实低EGFR蛋白表达病例的OS优于高EGFR蛋白表达病例。总体而言,这些数据表明EGFR蛋白表达是KRAS外显子2野生型结直肠癌西妥昔单抗治疗疗效的另一个阴性预测因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5728/7139947/87bf5c2d1a05/cancers-12-00614-g001.jpg

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