St James's Hospital, Dublin, Ireland.
Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Gastroenterology. 2018 Jun;154(8):2111-2121.e8. doi: 10.1053/j.gastro.2018.03.022. Epub 2018 Mar 11.
BACKGROUND & AIMS: Treatment with direct-acting antiviral (DAA) agents can reduce Model for End-Stage Liver Disease and Child-Pugh-Turcotte (CPT) scores in patients with decompensated cirrhosis caused by hepatitis C virus. However, many of these patients still die or require liver transplantation. We collected data on baseline features of patients and aimed to develop a scoring system to predict response to DAA therapy.
We performed a retrospective analysis of data from 4 trials on the effects of sofosbuvir-based therapy in patients with hepatitis C virus-associated decompensated cirrhosis (502 of CPT class B and 120 of CPT class C). In these trials, patients were given 12 or 24 weeks of treatment with ledipasvir, sofosbuvir, and ribavirin or velpatasvir, sofosbuvir, and/or ribavirin, or 48 weeks of treatment with sofosbuvir and ribavirin. We collected demographic, clinical, treatment response, and laboratory data from patients and tested their associations with patient outcomes at 36 weeks. The primary outcome was factors associated with reduction of CPT score to class A.
The presence of ascites or encephalopathy, serum level of albumin <3.5 g/dL or alanine aminotransferase <60 U/L, and body mass index >25 kg/m were associated with an increased risk of not achieving a reduction in CPT to class A, independent of sustained viral response to therapy. Serum level of albumin <2.8 g/dL and abnormal level of bilirubin were associated with an increased risk of liver transplantation or death. We developed a scoring system based on 5 baseline factors (body mass index, encephalopathy, ascites, and serum levels of alanine aminotransferase and albumin) associated significantly with patient outcomes, which we called the "BE3A score." For patients with scores of 4-5, the hazard ratio for reduction of CPT score to class A was 52.3 (95% confidence interval, 15.2-179.7).
We identified 5 baseline factors (body mass index, encephalopathy, ascites, and serum levels of alanine aminotransferase and albumin) associated with a reduction of CPT score to class A in patients with hepatitis C virus-associated decompensated cirrhosis receiving DAA therapy. We developed a predictive score using these factors, called the BE3A score, which can be used as a shared decision-making tool, quantifying the potential benefits of DAA therapy for patients with decompensated cirrhosis.
直接作用抗病毒(DAA)药物治疗可降低丙型肝炎病毒引起的失代偿性肝硬化患者的终末期肝病模型和 Child-Pugh-Turcotte(CPT)评分。然而,这些患者中仍有许多死亡或需要进行肝移植。我们收集了患者基线特征的数据,旨在开发一种评分系统来预测 DAA 治疗的反应。
我们对 4 项索非布韦治疗丙型肝炎病毒相关失代偿性肝硬化患者的试验数据进行了回顾性分析(CPT 分级 B 组 502 例,CPT 分级 C 组 120 例)。在这些试验中,患者接受 ledipasvir、索非布韦和利巴韦林或 velpatasvir、索非布韦和/或利巴韦林治疗 12 或 24 周,或索非布韦和利巴韦林治疗 48 周。我们收集了患者的人口统计学、临床、治疗反应和实验室数据,并在 36 周时检测了这些数据与患者结局的关系。主要结局是与 CPT 评分降至 A 级相关的因素。
腹水或脑病的存在、血清白蛋白水平<3.5 g/dL 或丙氨酸氨基转移酶<60 U/L、体重指数>25 kg/m2与未能降低 CPT 评分至 A 级的风险增加相关,与持续病毒应答治疗无关。血清白蛋白水平<2.8 g/dL 和胆红素水平异常与肝移植或死亡风险增加相关。我们基于与患者结局显著相关的 5 个基线因素(体重指数、脑病、腹水和血清丙氨酸氨基转移酶和白蛋白水平)建立了一个评分系统,称为“BE3A 评分”。对于评分 4-5 分的患者,CPT 评分降低至 A 级的风险比为 52.3(95%置信区间,15.2-179.7)。
我们确定了 5 个基线因素(体重指数、脑病、腹水、血清丙氨酸氨基转移酶和白蛋白水平)与丙型肝炎病毒相关失代偿性肝硬化患者接受 DAA 治疗后 CPT 评分降低至 A 级相关。我们使用这些因素开发了一个预测评分,称为 BE3A 评分,可作为一个共同决策工具,量化 DAA 治疗对失代偿性肝硬化患者的潜在益处。