Development of hepatocellular carcinoma in patients with chronic hepatitis C who had sustained viral response following direct-acting antiviral therapy.
Berat Ebik, Mustafa Aygan, Elif Tugba Tuncel, Huseyin Kacmaz, Nazim Ekin, Medeni Arpa, Kendal Yalcin
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引用次数: 0
Abstract
Background and aim: Several studies have suggested that treatment with direct-acting antivirals (DAAs) in patients with chronic hepatitis C virus (HCV) may be associated with an increased risk of developing hepatocellular carcinoma (HCC). We investigated the incidence and risk factors of HCC in HCV patients who achieved a sustained virologic response (SVR) following DAA therapies.
Materials and methods: The medical data of patients who were diagnosed with HCV and received DAA therapy in two tertiary centers in Turkey were retrospectively collected.
Results: Among them, 75 patients (52.4%) were noncirrhotic and 68 patients (47.6%) were cirrhotic. The overall SVR rate was 97.2% (139/143). It was 100% in noncirrhotic and 94.1% in cirrhotic patients. HCC was developed in 5 (7.4%) patients, all of whom had baseline cirrhosis. The annual rate of HCC occurrence was 2.94%, and the 5-year cumulative incidence of HCC was 7.3%. The mean Child-Pugh score (CPS) and Model for End-Stage Liver Disease (MELD) score significantly decreased after DAA treatment (CPS 7.0 vs 5.9, p=0.001; MELD 10.8 vs 9.5, p=0.003).
Conclusion: There was no significant increase in the rate of HCC in cirrhotic HCV patients treated with DAAs. This treatment led to a remarkably high SVR rate and lowered CPS and MELD scores in cirrhotic HCV patients.
背景和目的:几项研究表明,直接作用抗病毒药物(DAAs)治疗慢性丙型肝炎病毒(HCV)患者可能与发生肝细胞癌(HCC)的风险增加有关。我们调查了在接受DAA治疗后获得持续病毒学应答(SVR)的HCV患者中HCC的发生率和危险因素。材料与方法:回顾性收集土耳其两所三级中心诊断为HCV并接受DAA治疗的患者的医疗资料。结果:其中无肝硬化75例(52.4%),肝硬化68例(47.6%)。总SVR率为97.2%(139/143)。非肝硬化患者为100%,肝硬化患者为94.1%。5例(7.4%)患者发生HCC,均为基线肝硬化。HCC年发生率为2.94%,5年累计发病率为7.3%。DAA治疗后平均Child-Pugh评分(CPS)和终末期肝病模型(MELD)评分显著降低(CPS 7.0 vs 5.9, p=0.001;MELD 10.8 vs 9.5, p=0.003)。结论:接受DAAs治疗的肝硬化HCV患者HCC发生率无显著升高。这种治疗可显著提高肝硬化HCV患者的SVR率,降低CPS和MELD评分。