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Published on: June 26, 2020
Follow-up of chronic paediatric hepatitis C virus in a low-/middle-income country
Mortada El-Shabrawi1, Sherif Baroudy1, Fetouh Hassanin2
1Cairo University, Cairo, Egypt.
Insights
Direct-acting antiviral (DAA) therapies like Sofosbuvir/Ledipasvir and Sofosbuvir/Daclatasvir demonstrate superior efficacy and safety for treating chronic hepatitis C virus (HCV) infection in children compared to Interferon/Ribavirin.
Area of Science:
- Hepatology
- Virology
- Pediatric Infectious Diseases
Background:
- Chronic hepatitis C virus (HCV) infection poses long-term health risks.
- Effective treatment options are crucial for pediatric patients to achieve sustained virologic response (SVR).
- Evaluating treatment outcomes and safety profiles in children is essential for guiding clinical practice.
Purpose of the Study:
- To compare the efficacy and safety of Interferon (IFN) plus Ribavirin (RBV) versus direct-acting antiviral (DAA) therapies in pediatric outpatients with chronic HCV.
- To assess sustained virologic response (SVR) rates and adverse events in children treated with different HCV regimens.
Main Methods:
- A cohort of 60 pediatric patients (6-18 years) with chronic HCV infection was studied.
- Group 1 (21 patients) received IFN/RBV therapy.
- Group 2 (39 patients) received dual DAA therapy (Sofosbuvir/Ledipasvir or Sofosbuvir/Daclatasvir).
Main Results:
- IFN/RBV therapy achieved a 57.1% SVR rate, with all patients experiencing short-term side effects. Six patients required subsequent DAA treatment.
- DAA therapies (Sofosbuvir/Ledipasvir and Sofosbuvir/Daclatasvir) resulted in 100% SVR.
- DAA treatment showed negligible short-term side effects in most patients, with fibrosis regression observed in some cases.
Conclusions:
- Dual DAA therapy (Sofosbuvir/Ledipasvir and Sofosbuvir/Daclatasvir) is highly effective and safe for treating chronic HCV in children.
- IFN/RBV therapy is less effective and associated with more side effects in pediatric HCV patients.
- Successful HCV treatment may halt or even reverse liver fibrosis in children.
Aim:
Follow-up of chronic hepatitis C virus (HCV) infection following Interferon (IFN) plus Ribavirin (RBV) or direct-acting antiviral (DAA) drug therapy in a cohort of paediatric outpatients as confirmed by a sustained virologic response (SVR).
Methods:
This study included a cohort of 60 patients (6-18 years), divided into 2 groups: Group 1:21 patients who completed treatment with IFN/RBV. Group 2:39 treated with dual DAA therapy: 19 with Sofosbuvir/Ledipasvir (SOF/LED) and 20 with Sofosbuvir/Daclatasvir (SOF/DCV).
Results:
Group 1:12 (57.1%) were cured, six were IFN/RBV treatment failure then subsequently treated with DAAs successfully, and three had liver transplants. IFN/RBV side effects were reported in all patients; however, fibrosis regressed in two cured patients. Group 2: all were cured. HCV RNA became negative in all DAAs-treated patients at weeks 2, 4 and 12 of treatment (100%) as well as SVR after 12 weeks (100%). Thirty patients reported no adverse side effects whereas only nine suffered minor side effects.
Conclusions:
In our cohort, SOF/LED therapy and SOF/DCV therapy were extremely safe and effective with 100% SVR and negligible short-term side effects. IFN/RBV therapy was much less effective (SVR 57.1%) and accompanied with short-term side effects. Fibrosis might stop and even regress with successful treatment.
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