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Road to elimination of HCV: Clinical challenges in HCV management

机译:消除丙型肝炎病毒之路:丙型肝炎管理的临床挑战

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Abstract Since its discovery in 1989, the road to a cure for hepatitis C virus (HCV) has been slow, but most patients can now expect to achieve a sustained virological response (SVR). With direct‐acting antiviral (DAA) combination therapies such as glecaprevir/pibrentasvir and velpatasvir/sofosbuvir, 98 of patients successfully eradicate the virus, even if previous treatments failed or if resistance‐associated substitutions (RASs) are present. Adverse events are rare or mild, and patients with compensated cirrhosis and other co‐morbidities are often eligible for treatment. However, a small number of patients fail to eradicate the virus even after retreatment. The cause of failure is mainly due to emergence of NS5A P32 deletion mutants after initial DAA therapy in genotype 1b patients, although the reason is unknown for some patients. Alternative therapies that do not rely on NS5A inhibitors, such as sofosbuvir plus ribavirin, can be attempted in these patients. While scaled‐up treatment efforts present a challenge, another problem is that many carriers are unaware of their infection. Long‐term damage to the liver becomes irreversible, and patients who are not diagnosed in time can develop liver cancer or liver failure even after eliminating the virus. The long‐term costs of treatment of advanced liver disease in undiagnosed patients relative to the immediate costs of DAA therapy should be considered. As no vaccine is yet available, eventual elimination of the virus requires identifying and treating undiagnosed cases and screening of high‐risk populations such as injection drug users and men who have sex with men and female sex workers.
机译:摘要 自1989年发现以来,丙型肝炎病毒(HCV)的治愈之路一直很缓慢,但大多数患者现在可以期望获得持续的病毒学反应(SVR)。使用直接作用抗病毒 (DAA) 联合疗法,例如 glecaprevir/pibrentasvir 和 velpatasvir/sofosbuvir,98% 的患者成功根除病毒,即使先前的治疗失败或存在耐药相关替代 (RAS)。不良事件很少见或轻微,代偿期肝硬化和其他合并症患者通常有资格接受治疗。然而,少数患者即使在再次治疗后也无法根除病毒。失败的原因主要是由于基因型 1b 患者初始 DAA 治疗后出现 NS5A P32 缺失突变体,但部分患者原因尚不清楚。对于这些患者,可以尝试不依赖 NS5A 抑制剂的替代疗法,例如索非布韦加利巴韦林。虽然扩大治疗工作是一项挑战,但另一个问题是许多携带者没有意识到他们的感染。对肝脏的长期损害变得不可逆转,即使消灭了病毒,未及时诊断的患者也可能发展为肝癌或肝功能衰竭。应考虑未确诊患者晚期肝病治疗的长期成本相对于 DAA 治疗的直接成本。由于尚无疫苗可用,最终消除该病毒需要识别和治疗未确诊病例,并筛查高危人群,如注射吸毒者、男男性行为者和女性性工作者。

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