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卡瑞利珠单抗联合TACE对伴微血管侵犯肝细胞癌患者肿瘤标志物、血管生成因子和血清PD-1、PD-L1的影响
引用本文:汪景洲,王宇鹏,刘航成,梁 峰,赵清涛.卡瑞利珠单抗联合TACE对伴微血管侵犯肝细胞癌患者肿瘤标志物、血管生成因子和血清PD-1、PD-L1的影响[J].现代生物医学进展,2024(9):1678-1681.
作者姓名:汪景洲  王宇鹏  刘航成  梁 峰  赵清涛
作者单位:中国人民解放军联勤保障部队第九八〇医院肝胆胰脾科 河北 石家庄 050000;中国人民解放军联勤保障部队第九八〇医院肿瘤科 河北 石家庄 050000
基金项目:河北省卫生健康委员会医学科学研究计划项目(20220248)
摘    要:摘要 目的:观察卡瑞利珠单抗联合肝动脉化疗栓塞术(TACE)对伴微血管侵犯肝细胞癌(HCC)患者肿瘤标志物、血管生成因子和血清程序性细胞死亡蛋白-1(PD-1)、程序性死亡配体-1(PD-L1)的影响。方法:根据随机数字表法将2021年6月~2023年7月期间我院收治的121例伴微血管侵犯HCC患者分为对照组(n=60,接受肝癌根治术和TACE治疗)和研究组(n=61,对照组的基础上接受卡瑞利珠单抗治疗)。对比两组疗效、血清肿瘤标志物水平甲胎蛋白(AFP)、癌胚抗原(CEA)、异常凝血酶原(PIVKA-Ⅱ)、糖类抗原199(CA199)]、血管生成因子水平血管内皮生长因子受体2(VEGF-R2)、血管生成素-2(Ang-2)、血管内皮生长因子(VEGF)]、血清PD-1、PD-L1水平、不良反应。结果:与对照组相比,研究组的临床总有效率更高(P<0.05)。与对照组治疗后相比,研究组CEA、AFP、CA199、PIVKA-Ⅱ、VEGF、VEGF-R2、Ang-2、PD-1、PD-L1更低(P<0.05)。两组不良反应发生率比较未见差异(P>0.05)。结论:卡瑞利珠单抗联合TACE治疗伴微血管侵犯HCC患者,可改善血清肿瘤标志物,可抑制血管生成和降低血清PD-1、PD-L1水平,有效控制疾病进展。

关 键 词:卡瑞利珠单抗    TACE  微血管侵犯  肝细胞癌  肿瘤标志物  血管生成因子  PD-1  PD-L1
收稿时间:2023/12/26 0:00:00
修稿时间:2024/1/22 0:00:00

Effect of Carrelizumab Combined with TACE on Tumor Markers, Angiogenesis Factors and Serum PD-1 and PD-L1 in Patients with Hepatocellular Carcinoma with Microvascular Invasion
Abstract:ABSTRACT Objective: To observe the effects of carrelizumab combined with transcatheter arterial chemoembolization (TACE) on tumor markers, angiogenic factors, serum programmed cell death protein-1 (PD-1) and programmed death ligand-1 (PD-L1) in patients with hepatocellular carcinoma (HCC) with microvascular invasion. Methods: 121 HCC patients with microvascular invasion who were admitted to our hospital from June 2021 to July 2023 were divided into control group (n=60, receiving radical resection of liver cancer and TACE treatment) and study group (n=61, receiving carrelizumab treatment on the basis of control group) according to the random number table method. The efficacy, serum tumor marker levels alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), abnormal prothrombin (PIVKA-II), carbohydrate antigen 199 (CA199)], angiogenesis factor levels vascular endothelial growth factor receptor 2 (VEGF-R2), angiopoietin-2 (Ang-2), vascular endothelial growth factor (VEGF)], serum PD-1 and PD-L1 levels, adverse reactions were compared between two groups (P>0.05). Results: Compared with control group, the total clinical effective rate in study group was higher (P<0.05). Compared with control group after treatment, CEA, AFP, CA199, PIVKA-II, VEGF, VEGF-R2, Ang-2, PD-1 and PD-L1 in study group were lower(P<0.05). There was no difference in the incidence of adverse reactions between two groups(P>0.05). Conclusion: Carrelizumab combined with TACE in the treatment of HCC patients with microvascular invasion, which can improve the serum tumor markers, inhibit angiogenesis and reduce serum PD-1 and PD-L1 levels, and effectively control disease progression.
Keywords:Carrelizumab  TACE  Microvascular invasion  Hepatocellular carcinoma  Tumor markers  Angiogenic factors  PD-1  PD-L1
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