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Published on: September 30, 2021
Recent advances in the treatment of hepatitis C virus infection for special populations and remaining problems
1Department of Gastroenterology and Hepatology, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Insights
Direct-acting antivirals (DAAs) offer a safer and more effective treatment for Hepatitis C virus (HCV) infection in special populations, including those with HIV/HCV coinfection, post-liver transplant, and on dialysis. Ongoing research addresses challenges like drug resistance and HCC occurrence.
Area of Science:
- Hepatology and Viral Gastroenterology
- Infectious Diseases and Public Health
- Pharmacology and Therapeutics
Background:
- Hepatitis C virus (HCV) infection is a leading cause of liver cirrhosis, hepatocellular carcinoma (HCC), and liver transplantation (LT).
- High HCV prevalence exists in hemodialysis patients and those with human immunodeficiency virus (HIV) coinfection.
- Recurrent HCV infection post-LT and rapid fibrosis in HCV/HIV coinfection necessitate urgent treatment strategies.
Purpose of the Study:
- To review recent advances in Hepatitis C virus (HCV) treatment for special populations.
- To evaluate the efficacy and safety of direct-acting antivirals (DAAs) in HIV/HCV coinfection, post-liver transplant, and dialysis patients.
- To identify and discuss unresolved issues concerning DAA therapy in these groups.
Main Methods:
- Review of recent clinical trials and studies on direct-acting antiviral (DAA) therapies for Hepatitis C virus (HCV).
- Analysis of treatment outcomes, safety profiles, and adverse events in special patient populations.
- Examination of emerging challenges, including resistance-associated variants and HCC occurrence post-DAA therapy.
Main Results:
- Interferon (IFN)-based therapies demonstrated limited efficacy and significant adverse events in special populations.
- IFN-free DAA-based therapies show superior safety and therapeutic profiles compared to IFN-based treatments.
- Recent studies confirm high efficacy and safety of DAAs in HIV/HCV coinfection, post-LT, and dialysis patients, despite initial trial exclusions.
Conclusions:
- IFN-free DAA therapy represents a significant advancement in managing Hepatitis C virus (HCV) infection across diverse patient groups.
- Despite high efficacy, challenges such as drug resistance and post-treatment HCC require continued investigation and management strategies.
- Further research is essential to optimize DAA treatment protocols and address long-term outcomes in special populations.
Abstract:
Hepatitis C virus (HCV) infection is one of the primary causes of liver cirrhosis, hepatocellular carcinoma (HCC), and liver transplantation (LT). The rate of HCV infection is high in patients on hemodialysis and in patients infected with human immunodeficiency virus (HIV). In liver transplant patients with HCV infection, recurrent HCV infection of the transplanted liver is universal and results in rapid liver fibrosis progression. In patients with HCV/HIV coinfection as well, liver fibrosis advances rapidly. Thus, there is an urgent need for prompt HCV infection treatment in these special populations (i.e. HIV/HCV coinfection, HCV infection after LT, and dialysis patients). Interferon (IFN)-based therapy for HCV infection could not achieve a high rate of sustained viral response and could cause severe adverse events in the aforementioned special populations. Direct-acting antivirals (DAAs) have recently been developed, and clinical trials have shown that IFN-free DAA-based therapies are associated with a significantly better safety and therapeutic profile than IFN-based therapies. However, the majority of the initial DAA trials excluded special populations; thus, the efficacy and safety of IFN-free DAA-based therapy in special populations remained to be clearly established. Although recent clinical trials and clinical studies have shown the high efficacy and safety of this therapy even in special populations, several unresolved problems, including emergence of resistance-associated variants after failure to respond to DAAs and HCC occurrence after DAA therapy, still exist. Hence, in this review, we discuss the recent advances in anti-HCV therapy for special populations and the remaining problems regarding this therapy.
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