Ding Yun, Fu Yuanyuan, Wei Wei, Huang Weibin, Zheng Zhuojun, Zhang Dachuan, He Jiajia, Zheng Xiao, Wang Qi, Liu Yingting, Gu Wendong, Jiang Jingting
Department of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Jiangsu Engineering Research Center for Tumor Immunotherapy, Changzhou, China.
Transl Cancer Res. 2021 Jan;10(1):499-508. doi: 10.21037/tcr-20-3106.
The aim of the present study was to analyze the association of programmed cell death-ligand 1 (PD-L1) and vascular endothelial growth factor receptor 2 (VEGFR2) expression levels with clinicopathological characteristics and survival to provide a treatment strategy for rectal cancer.
Immunohistochemical staining of VEGFR2 and PD-L1 was carried out, and the association of PD-L1 and VEGFR2 expression levels with clinicopathological characteristics and survival were investigated in 77 pair-matched rectal cancer patients.
PD-L1 and VEGFR2 expression levels in surgical tumor tissues were higher than those in paired adjacent normal tissues, respectively (both P<0.05). The results of the 5-year overall survival (OS) analysis showed that patients with low VEGFR2 expression (66.7% 43.5%, P=0.042) and high tumor PD-L1 expression (63.9% 26.1%, P=0.001) in tumor tissues demonstrated significantly better OS. Patients with high TNM stage had poorer OS [hazard ratio (HR): 2.093, 95% confidence interval (CI): 1.027-4.087, P=0.030]. Similar results of poorer OS could be seen in patients with low tumor PD-L1 expression (HR: 3.365, 95% CI:1.747-6.481, P=0.005), as well as patients with high tumor VEGFR2 expression (HR: 0.418, 95% CI: 0.232-0.993, P=0.048).
The results indicated that tumor PD-L1 and VEGFR2 expression levels were associated with OS, and the combination of tumor PD-L1 and VEGFR2 levels might be an independent prognostic factor in rectal cancer.
本研究旨在分析程序性细胞死亡配体1(PD-L1)和血管内皮生长因子受体2(VEGFR2)表达水平与临床病理特征及生存率的相关性,从而为直肠癌提供治疗策略。
对VEGFR2和PD-L1进行免疫组织化学染色,并在77例配对的直肠癌患者中研究PD-L1和VEGFR2表达水平与临床病理特征及生存率的相关性。
手术切除的肿瘤组织中PD-L1和VEGFR2表达水平分别高于配对的相邻正常组织(均P<0.05)。5年总生存(OS)分析结果显示,肿瘤组织中VEGFR2低表达(66.7%对43.5%,P=0.042)和肿瘤PD-L1高表达(63.9%对26.1%,P=0.001)的患者OS明显更好。TNM分期高的患者OS较差[风险比(HR):2.093,95%置信区间(CI):1.027 - 4.087,P=0.030]。肿瘤PD-L1低表达患者(HR:3.365,95%CI:1.747 - 6.481,P=0.005)以及肿瘤VEGFR2高表达患者(HR:0.418,95%CI:0.232 - 0.993,P=0.048)也可见类似的OS较差结果。
结果表明肿瘤PD-L1和VEGFR2表达水平与OS相关,肿瘤PD-L1和VEGFR2水平的联合可能是直肠癌的一个独立预后因素。