Vo Thong Duy, Bui Van Thi Thu, Lam Huong Tu, Bui Quynh Thi Huong
Department of Internal Medicine, Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Department of Gastroenterology, University Medical Center Ho Chi Minh City, Ho Chi Minh City, Vietnam.
Pharmacol Res Perspect. 2024 Oct;12(5):e70007. doi: 10.1002/prp2.70007.
Direct-acting antivirals (DAAs) have revolutionized hepatitis C virus (HCV) treatment through their high cure rates and improved safety profiles. We aimed to evaluate the efficacy and safety, and identify the optimal combination, of DAAs for the treatment of chronic HCV. A retrospective study was conducted of 613 patients with chronic HCV who were treated with DAAs. Demographic, HCV genotype, treatment regimen, virological response, and adverse drug event (ADE) data were collected at the initial visit and 4, 8, 12, and 24 weeks later. The rapid virologic response (RVR) and sustained virologic response (SVR) rates were 90.4% and 97.8% for HCV genotype 1, 89.2% and 98.7% for genotype 6, 92.8% and 99% for genotype 2, and 90.9% and 100% for mixed genotype 2/6 or unspecified genotypes, respectively. There were no significant differences in the RVR and SVR rates for the various DAA regimens. The mean ALT, AST, and GGT activities decreased, and the PLT count increased during the treatments. ADEs occurred in 8% of the patients. The commonest ADEs were itching (3.1%), fatigue (1.8%), and dizziness (1.1%). None of the patients discontinued treatment because of an ADE. Posttreatment disease progression occurred in 7.7% of the patients, including liver fibrosis (3.6%), cirrhosis (1.1%), hepatocellular carcinoma (1.1%), and high alpha-fetoprotein (AFP) (1%). The factors associated with the achievement of RVR were low viral load, the use of sofosbuvir/ledipasvir or sofosbuvir/daclatasvir regimens, and a treatment duration of 12 weeks. No specific factors were found to be associated with the achievement of SVR. Posttreatment disease progression was associated with a high AFP and the use of sofosbuvir/ledipasvir. Thus, DAAs are highly effective and well-tolerated means of treating chronic HCV, and significantly improve patient outcomes. Their high efficacy and favorable safety profiles highlight the importance of early diagnosis and the use of personalized treatment strategies.
直接作用抗病毒药物(DAAs)通过其高治愈率和改善的安全性,彻底改变了丙型肝炎病毒(HCV)的治疗方式。我们旨在评估DAAs治疗慢性HCV的疗效和安全性,并确定最佳组合。对613例接受DAAs治疗的慢性HCV患者进行了一项回顾性研究。在初次就诊时以及4、8、12和24周后收集人口统计学、HCV基因型、治疗方案、病毒学反应和药物不良事件(ADE)数据。HCV 1型的快速病毒学反应(RVR)和持续病毒学反应(SVR)率分别为90.4%和97.8%,6型分别为89.2%和98.7%,2型分别为92.8%和99%,2/6混合型或未明确基因型分别为90.9%和100%。各种DAA方案的RVR和SVR率无显著差异。治疗期间,平均谷丙转氨酶(ALT)、谷草转氨酶(AST)和γ-谷氨酰转肽酶(GGT)活性降低,血小板计数增加。8%的患者发生了ADE。最常见的ADE是瘙痒(3.1%)、疲劳(1.8%)和头晕(1.1%)。没有患者因ADE而停药。7.7%的患者出现治疗后疾病进展,包括肝纤维化(3.6%)、肝硬化(1.1%)、肝细胞癌(1.1%)和高甲胎蛋白(AFP)(1%)。与实现RVR相关的因素是低病毒载量、使用索磷布韦/维帕他韦或索磷布韦/达卡他韦方案以及12周的治疗疗程。未发现与实现SVR相关的特定因素。治疗后疾病进展与高AFP和使用索磷布韦/维帕他韦有关。因此,DAAs是治疗慢性HCV的高效且耐受性良好的方法,并显著改善患者预后。它们的高疗效和良好的安全性凸显了早期诊断和使用个性化治疗策略的重要性。