红细胞生成素的组织表达预测透明细胞肾细胞癌的存活率。

Daniel Beltrame Ferreira, Walter Henriques da Costa, Diego Abreu Clavijo, Ricardo Decia, Isabela Werneck Cunha, Luciana Schultz, Rafael Malagoli Rocha, Gustavo Cardoso Guimarães, Stênio de Cássio Zequi
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引用次数: 4

摘要

目的:探讨免疫组织化学促红细胞生成素(EPO)在透明细胞肾细胞癌(ccRCC)中的表达、与主要临床病理指标的关系及其对预后的影响。方法:对1989年至2009年间接受手术治疗的220例肾细胞癌(RCC)患者进行多机构研究。所有病例均由一名病理学家复查,并使用组织芯片分析EPO的免疫组织化学反应性。结果:共纳入176例ccRCC患者,平均随访48个月。在评估的肿瘤中,47例(26.7%)为EPO阴性表达,129例(73.3%)为阳性表达。EPO表达与偶发肿瘤(p = 0.016)、肿瘤大小(p = 0.015)、Karnofsky性能评分(KPS) (p = 0.016)、输血(p = 0.009)和肾上腺受损伤(p = 0.038)相关。EPO阳性和阴性患者的中位年龄分别为56.2岁和66.6岁。免疫组织化学EPO表达影响总生存(OS)和疾病特异性生存(DSS)率。EPO表达阳性和阴性患者的DSS分别为85.3%和76.1% (p = 0.044)。在一项多因素分析中,EPO表达缺失被证明是一个不良的预后因素,并对生存率产生负面影响(p结论:肿瘤EPO表达缺失是一个独立的预测因素,对生存率有负面影响。在ccRCC患者的治疗中,EPO作为可能的标志物的使用需要进一步的研究和更好地理解EPO在肿瘤生物学中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tissue Expression of Erythropoietin Predicts Survival Rates in Clear Cell Renal Cell Carcinoma.

Tissue Expression of Erythropoietin Predicts Survival Rates in Clear Cell Renal Cell Carcinoma.

Tissue Expression of Erythropoietin Predicts Survival Rates in Clear Cell Renal Cell Carcinoma.

Objective: To evaluate immunohistochemical erythropoietin (EPO) expression in clear cell renal cell carcinoma (ccRCC), its association with major clinicopathological variables and its prognostic impact.

Methods: A total of 220 patients with renal cell carcinoma (RCC) surgically treated between 1989 and 2009 were evaluated in this multi-institutional study. All the cases were reviewed by a single pathologist and the immunohistochemical reactivity to EPO was analysed using tissue microarray.

Results: A total of 176 patients with ccRCC were considered, with an average of 48 months of follow-up. Of the tumours evaluated, 47 (26.7%) were negative for EPO expression, and 129 (73.3%) were positive. EPO expression was associated with incidental tumour (p = 0.016), tumour size (p = 0.015), Karnofsky Performance Score (KPS) (p = 0.016), blood transfusion (p = 0.009) and adrenal involvement (p = 0.038). The median ages of the patients with positive and negative EPO expression were 56.2 years and 66.6 years. Immunohistochemical EPO expression affected overall survival (OS) and disease-specific survival (DSS) rates. The DSS rates of the patients whose tissue was positive and negative for EPO expression were 85.3% and 76.1%, respectively (p = 0.044). In a multivariate analysis, the absence of EPO expression proved to be a bad prognostic factor and negatively affected the OS (p < 0.001) and DSS (p < 0.001) rates.

Conclusion: The absence of tumour EPO expression is an independent predictive factor with a negative effect on survival rates. The use of EPO as possible marker in the management of ccRCC patients requires further studies and a better understanding of the role of EPO in tumour biology.

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