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Prognosis of Patients with Chronic Hepatitis C Genotype 1b Infection Treated Using Daclatasvir/Asunaprevir after
Jae-Hyun Yoon1, Sung-Eun Kim2, Su-Hyeon Cho1
1Department of Internal Medicine, School of Medicine, Chonnam National University Hospital, Gwangju 61469, Republic of Korea.
Insights
Patients treated with daclatasvir/asunaprevir for chronic hepatitis C achieved sustained virologic response, but a risk of hepatocellular carcinoma remains. Older age and cirrhosis are key risk factors for developing liver cancer post-treatment.
Area of Science:
- Hepatology
- Virology
- Oncology
Background:
- Direct-acting antiviral (DAA) therapy offers a cure for chronic hepatitis C (CHC).
- Daclatasvir (DCV)/asunaprevir (ASV) was the first interferon-free DAA regimen available in Korea.
- Sustained virologic response (SVR) after DAA treatment is associated with favorable patient prognoses.
Purpose of the Study:
- To investigate the long-term prognosis of patients with CHC who achieved SVR after DCV/ASV treatment.
- To identify risk factors for hepatocellular carcinoma (HCC) development in this patient cohort.
Main Methods:
- A multicenter prospective observational study was conducted.
- 302 patients with CHC who achieved SVR following DCV/ASV therapy were included.
- Hepatocellular carcinoma (HCC) occurrence was the primary endpoint, monitored annually over a median follow-up of 38 months.
Main Results:
- Hepatocellular carcinoma (HCC) developed in 5.3% of patients within six years post-SVR.
- Patients who developed HCC were older and had higher rates of cirrhosis, elevated alpha-fetoprotein, and higher FIB-4 scores.
- Cox proportional hazards analysis identified age > 71 years and the presence of cirrhosis as significant risk factors for HCC (p=0.005 and p=0.035, respectively).
Conclusions:
- While DCV/ASV therapy leads to good prognoses for CHC patients achieving SVR, a residual risk of HCC exists.
- Older age and pre-existing cirrhosis are critical factors increasing HCC risk after treatment.
- Recommendations include initiating treatment at younger ages and implementing regular post-SVR surveillance for HCC.
Abstract:
Aim and Objectives: Direct-acting antiviral (DAA) therapy can cure chronic hepatitis C (CHC), and daclatasvir (DCV)/asunaprevir (ASV) was the first interferon-free DAA therapy introduced in Korea. Patients who achieve sustained virologic response (SVR) after DAA treatment are expected to have good prognoses. Therefore, in this study, we aimed to investigate the prognosis of these patients. Materials and Methods: This multicenter prospective observational study included patients with CHC who achieved SVR after DCV/ASV treatment. The primary endpoint was hepatocellular carcinoma (HCC) occurrence, which was reviewed annually. Results: We included 302 patients (median follow-up duration: 38 [16.5-60.0] months; median age: 58 [49-67] years) in the study. Cirrhosis was observed in 103 patients (34.1%), and the median Child-Pugh score was 5.0. HCC occurred in 16 patients (5.3%) within six years post-SVR; these patients were older and had higher cirrhosis prevalence, alpha-fetoprotein levels, and fibrosis-4 index scores than did those without HCC development. Cox proportional hazards analysis revealed that age > 71 years (p = 0.005) and cirrhosis (p = 0.035) were significant risk factors for HCC occurrence. Conclusions: Although the prognoses of patients who achieved SVR with DCV/ASV therapy were generally good, the risk for HCC was present, especially in older patients and in those with cirrhosis. Hence, early treatment at younger ages and regular follow-up surveillance after achieving SVR are warranted.
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