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一线舒尼替尼治疗转移性透明细胞肾细胞癌患者中 VEGF、CD31 和 Ang-1 的预后和预测意义。

Prognostic and predictive significance of VEGF, CD31, and Ang-1 in patients with metastatic clear cell renal cell carcinoma treated with first-line sunitinib.

机构信息

Oncology Clinic, University Clinical Hospital Mostar, Mostar, Bosnia and Herzegovina.

Laboratory of Morphology, Department of Histology and Embryology, School of Medicine, University of Mostar, Mostar, Bosnia and Herzegovina.

出版信息

Biomol Biomed. 2023 Feb 1;23(1):161-169. doi: 10.17305/bjbms.2022.7675.

Abstract

The most common type of renal cell carcinoma (RCC) is clear cell renal cell carcinoma (ccRCC), which has a high metastatic potential. Even though the International Metastatic RCC Database Consortium (IMDC) risk model is conventionally utilized for selection and stratification of patients with metastatic RCC (mRCC), there remains an unmet demand for novel prognostic and predictive markers. The goal of this study was to analyze the expression of Vascular endothelial growth factor (VEGF), Cluster of Differentiation 31 (CD31) to determine microvessel density, and Angiopoietin-1 (Ang-1) in primary kidney tumors, as well as their predictive and prognostic value in patients with metastatic ccRCC (mccRCC) who were treated with first-line sunitinib. The study included 35 mccRCC patients who were treated with first-line sunitinib in period between 2009 and 2019. Immunofluorescence was used to examine biomarker expression in tissue specimens of the primary tumor and surrounding normal kidney tissue. Median disease-free survival (DFS) was longer in patients with negative and low tumor VEGF score than in patients with medium tumor VEGF score (p=0.02). Those with low tumor CD31 expression had a longer median DFS than patients with high tumor CD31 expression (p=0.019). There was no correlation between Ang-1 expression and DFS. The expression of biomarkers in normal kidney tissue was significantly lower than in tumor tissue (p<0.001). In conclusion, higher VEGF scores and greater CD31 expression were associated with longer DFS, but neither of these biomarkers correlated with progression-free survival or overall survival.

摘要

最常见的肾细胞癌 (RCC) 类型是透明细胞肾细胞癌 (ccRCC),它具有很高的转移潜能。尽管国际转移性肾细胞癌数据库联盟 (IMDC) 风险模型常用于选择和分层转移性肾细胞癌 (mRCC) 患者,但仍需要新的预后和预测标志物。本研究旨在分析血管内皮生长因子 (VEGF)、分化簇 31 (CD31) 的表达以确定微血管密度,以及血管生成素-1 (Ang-1) 在原发肾肿瘤中的表达,并分析其在接受一线舒尼替尼治疗的转移性 ccRCC (mccRCC) 患者中的预测和预后价值。本研究纳入了 2009 年至 2019 年间接受一线舒尼替尼治疗的 35 例 mccRCC 患者。免疫荧光法用于检测原发肿瘤和周围正常肾组织标本中的生物标志物表达。无复发生存期 (DFS) 的中位数在肿瘤 VEGF 评分阴性和低的患者中长于肿瘤 VEGF 评分中等的患者 (p=0.02)。肿瘤 CD31 低表达的患者的中位 DFS 长于肿瘤 CD31 高表达的患者 (p=0.019)。Ang-1 表达与 DFS 无相关性。正常肾组织中生物标志物的表达明显低于肿瘤组织 (p<0.001)。结论:较高的 VEGF 评分和更高的 CD31 表达与更长的 DFS 相关,但这些生物标志物均与无进展生存期或总生存期无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f18/9901909/b5c24df08b28/bjbms-2022-7675f1.jpg

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