摘要【目的】研究丙型肝炎病毒(HCV)直接抗病毒药物(DAA)抗病毒干预获得持续病毒学应答(SVR)后发生肝细胞肝癌(HCC)患者的临床特征。【方法】纳入本院130例HCV感染患者作为研究对象,所有患者均接受HCV抗病毒治疗,记录SVR情况。出院后随访记录HCC发生率。根据是否发生HCC,将获得SVR的患者分为观察组(发生HCC)和对照组(未发生HCC)。比较两组患者基本资料和临床病理特点,采用Cox多因素风险模型探讨经HCV抗病毒干预后获得SVR患者发生HCC的高危因素。【结果】130例患者中98例达到SVR效果,SVR率为75.38%,在98例患者中,随访期间共发生HCC 6例,发生率6.12%。不同预后患者DAA治疗情况、肝脏状态、谷草转氨酶(AST)、谷丙转氨酶(ALT)及甲胎蛋白(AFP)水平比较差异均有显著性( P <0.05)。Cox多因素风险分析显示ADD治疗情况、肝脏状态及AFP水平是HCV抗病毒治疗获得SVR的患者后发生HCC的危险因素(均 P <0.05)。【结论】对于HCV抗病毒干预治疗后达到SVR的患者,患者DAA治疗情况、肝脏状态及AFP水平是影响患者发生HCC的独立因素。
Abstract:【Objective】To investigate the clinical characteristics of hepatitis C virus (HCV) treated with direct-acting antivirals(DAA) patients with hepatocellular carcinoma (HCC) during the sustained virological response (SVR) after antiviral intervention. 【Methods】 A total of 130 patients with HCV infection in our hospital were recruited in the study. All patients were received HCV antiviral therapy and the SVR rate was recorded. The incidence of HCC were followed up after discharge. According to the occurrence of HCC, patients with SVR were further divided into the observation group (occurrence of HCC) and the control group (no occurrence of HCC).The basic data and clinicopathological characteristics were compared between the two groups. The Cox multivariate risk model was used to explore the high risk factors of HCC in patients with SVR after HCV antiviral intervention. 【Results】Among 130 patients with HCV,98 required SVR after HCV antiviral intervention. The SVR rate was 75.38%.There were 6 cases of HCC occurred during the follow-up period, which was 6.12% (6/98).There were significant differences in direct antiviral drugs (DAA) treatment, liver status, AST, ALT and AFP levels among patients with different prognosis, the difference were statistically significant ( P <0.05).The Cox multivariate risk analysis showed that the DAA treatment, liver status and AFP level were the risk factors for HCC after SVR ( P <0.05). 【Conclusion】 The DAA treatment, liver status and AFP level are the independent factors, which affect the occurrence of HCC for the patients with SVR after antiviral therapy.
刘冬宇, 白劼, 张文华, 郝艳霞. 丙型肝炎病毒患者抗病毒干预持续应答后发生肝细胞肝癌的临床特征*[J]. 医学临床研究, 2021, 38(3): 356-358.
LIU Dong-yu, BAI Jie, ZHANG Wen-hua, et al. Clinical Analysis of Hepatitis C Virus Patients with Hepatocellular Carcinoma during Sustained Virological Response after Antiviral Intervention. JOURNAL OF CLINICAL RESEARCH, 2021, 38(3): 356-358.
[1] 甘志超,刘莹,赵冰红,等.丙型肝炎患者自身抗体检出率、丙肝病毒载量及肝功能间的相关性[J].现代检验医学杂志,2016,31(3):108-110. [2] 穆彩琴. 丙型肝炎肝硬化抗病毒治疗SVR率相关因素研究[J].中华实验和临床病毒学杂志,2016,30(5):477-480. [3] 王其亮,郜玉峰.直接作用抗病毒药物在人类免疫缺陷病毒合并丙型肝炎病毒感染者中的应用[J].中华传染病杂志,2015,33(9):569-571. [4] 李砚,刘蕾,罗书兰,等.丙型肝炎直接抗病毒治疗与肝癌发生及复发的关系[J].临床肝胆病杂志,2018,34(2):410-413. [5] 路遥,郝红晓,申戈,等.慢性丙型肝炎干扰素强化治疗失败患者的PR联合DAA再治疗研究[J].中华实验和临床病毒学杂志,2018,32(1):66-69. [6] 中华医学会肝病学分会.丙型肝炎防治指南[J].中华内科杂志,2004,43(7):551-555. [7] 慢性丙型肝炎抗病毒治疗专家委员会.慢性丙型肝炎抗病毒治疗专家共识[J].中华实验和临床感染病杂志,2009,3(3):343-353. [8] Adhoute X, Penaranda G, Raoul JL, et al . Hepatocellular carcinoma recurrence in hepatitis C virus-related cirrhosis treated with direct-acting antivirals:a case-control study[J]. Eur J Gastroenterol Hepatol, 2018,30(4):368-375. [9] 安子英. 我国慢性丙型肝炎患者真实世界中直接抗病毒药物治疗方案的选择与评价[J].临床肝胆病杂志,2018,34(2):233-237.[10] 杨颖,党双锁.丙型肝炎直接抗病毒药物安全性应用进展[J].世界华人消化杂志,2017,25(8):12-22. [11] 喻一奇,张文宏.HCV感染者接受直接抗病毒药物治疗期间发生肝细胞癌风险[J].肝脏,2017,22(12):1083-1084. [12] Cardoso H, Vale AM,Rodrigues S, et al . High incidence of hepatocellular carcinoma following successful interferon-free antiviral therapy for hepatitis C associated cirrhosis[J]. J Hepatol, 2016,65(5):1070-1071. [13] 曾庆磊,吕君,付艳玲,等.慢性丙型肝炎经抗病毒治疗后获得持续病毒学应答患者发生肝细胞癌危险因素预测分析[J].中华传染病杂志,2016,34(3):160-164. [14] Zhu M, Li W, Lu Y, et al . HBx drives alpha fetoprotein expression to promote initiation of liver cancer stem cells through activating PI3K/AKT signal pathway[J]. Int J Cancer, 2017,140(6):1346-1355.