Zanaga L P, Santos A G, Ataíde E C, Boin I F S F, Stucchi R S B
Disciplina de Infectologia, Departamento de Clínica Médica, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brasil.
Grupo de Fígado, Hipertensão Portal e Transplante Hepático, Disciplina de Moléstias do Aparelho Digestivo, Departamento de Cirurgia, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brasil.
Braz J Med Biol Res. 2019;52(8):e8519. doi: 10.1590/1414-431X20198519. Epub 2019 Aug 5.
Recurrent hepatitis C (HCV) after liver transplantation (LT) is an important cause of morbidity and mortality. Antiviral treatment is recommended to avoid unfavorable outcomes. Direct-acting antivirals (DAA) have transformed HCV treatment, with higher efficacy and fewer side-effects than interferon-based therapies traditionally used. To evaluate DAA treatment outcomes at a Brazilian transplant unit, data of patients who finished HCV treatment at the Liver Transplant Unit of the University of Campinas were analyzed. Treatment consisted of sofosbuvir, daclatasvir, and ribavirin, for 12 or 24 weeks, according to the national guidelines. Fifty-five patients completed antiviral treatment and 54 had HCV-viral load results available. The majority of patients were male (78%), 58 years old on average, 65% had hepatocellular carcinoma (HCC) before LT, and 67% were interferon treatment-experienced. Most patients had HCV genotype 1 (65%), 35% had genotype 3, and started treatment on an average of 38 months after LT (range: 2-228). Fifty-eight percent were treated for 12 weeks and 42% for 24 weeks, using a mean dose of ribavirin of 10.1 mg/kg (4.2-16.1). There were no treatment interruptions due to serious side effects. The sustained virological response rate was 98%. Only one patient relapsed, a genotype 3 cirrhotic treated for 12 weeks. The average follow-up after starting antivirals was 20 months. There were no recurrences of HCC, but there was one rejection episode and one cirrhosis decompensation episode, both 12 weeks after treatment. DAA treatment is safe and effective in the post-LT setting and was not associated to HCC recurrence in the cohort studied.
肝移植(LT)后丙型肝炎病毒(HCV)复发是发病和死亡的重要原因。建议进行抗病毒治疗以避免不良后果。直接抗病毒药物(DAA)改变了HCV的治疗方式,与传统使用的基于干扰素的疗法相比,疗效更高且副作用更少。为了评估巴西一家移植单位的DAA治疗效果,分析了坎皮纳斯大学肝移植科完成HCV治疗的患者数据。根据国家指南,治疗方案为索磷布韦、达卡他韦和利巴韦林,疗程为12周或24周。55例患者完成了抗病毒治疗,54例有HCV病毒载量结果。大多数患者为男性(78%),平均年龄58岁,65%在肝移植前患有肝细胞癌(HCC),67%有干扰素治疗史。大多数患者为HCV基因1型(65%),35%为基因3型,平均在肝移植后38个月开始治疗(范围:2 - 228个月)。58%的患者接受了12周治疗,42%接受了24周治疗,利巴韦林平均剂量为10.1 mg/kg(4.2 - 16.1)。没有因严重副作用而中断治疗的情况。持续病毒学应答率为98%。只有1例患者复发,该患者为基因3型肝硬化,接受了12周治疗。开始抗病毒治疗后的平均随访时间为20个月。没有HCC复发,但有1例排斥反应和1例肝硬化失代偿事件,均发生在治疗后12周。在肝移植后的情况下,DAA治疗安全有效,在所研究的队列中与HCC复发无关。