By 
                  Liz Highleyman
                  
                   Studies 
                  of combination interferon-based therapy for chronic 
                  hepatitis C usually focus on adults, who typically demonstrate 
                  sustained virological response 
                  (SVR) rates of just under 50% for HCV 
                  genotype 1 and 70%-80% for genotypes 
                  2 or 3 using a standard regimen of pegylated 
                  interferon plus ribavirin for 48 or 24 weeks, respectively. 
                  Treatment of children with hepatitis C has not been as extensively 
                  studied.
Studies 
                  of combination interferon-based therapy for chronic 
                  hepatitis C usually focus on adults, who typically demonstrate 
                  sustained virological response 
                  (SVR) rates of just under 50% for HCV 
                  genotype 1 and 70%-80% for genotypes 
                  2 or 3 using a standard regimen of pegylated 
                  interferon plus ribavirin for 48 or 24 weeks, respectively. 
                  Treatment of children with hepatitis C has not been as extensively 
                  studied.
                  
                  In the present study, Etienne Sokal from Catholic University 
                  Louvain in Belgium and an international team of colleagues evaluated 
                  the safety and efficacy of pegylated 
                  interferon alfa-2a (Pegasys) plus ribavirin in previously 
                  untreated HCV antibody positive children with detectable HCV 
                  RNA viral load.
                  
                  This prospective analysis included 18 children with HCV genotypes 
                  2 or 3, who were treated for 24 weeks, and 47 children with 
                  harder-to-treat genotypes 1, 4, 5, or 6, who were treated for 
                  48 weeks. 
                  
                  Results
                
                   
                    |  | 83% 
                      of the genotype 2/3 children and 57% of the genotype 1/4/5/6 
                      children achieved early virological response at week 12. | 
                   
                    |  | End-of-treatment 
                      response rates were 94% (at week 24) and 57% (at week 48), 
                      respectively. | 
                   
                    |  | Relapse 
                      rates were low, with 89% of easier-to-treat participants 
                      and 57% of hard-to-treat children achieving sustained response 
                      at 24 weeks after completion of therapy. | 
                   
                    |  | 10 
                      participants overall (15%) stopped treatment prematurely 
                      -- 2 due to serious adverse events and 8 due to lack of 
                      virological response at week 24. | 
                   
                    |  | 15 
                      children overall (23%) had their pegylated interferon or 
                      ribavirin doses adjusted -- 11 (17%) due to neutropenia 
                      and 3 (5%) due to anemia. | 
                   
                    |  | The 
                      most common treatment-related adverse events included: | 
                   
                    |  | 
                         
                          |  | Fever 
                            and flu-like symptoms (54%); |   
                          |  | Abdominal 
                            pain (38%); |   
                          |  | Irritability, 
                            depression, or mood changes (34%); |   
                          |  | Dermatitis 
                            (29%); |   
                          |  | Vomiting 
                            (23%); |   
                          |  | Loss 
                            of appetite (22%). |  | 
                   
                    |  | Interferon-based 
                      treatment had no observed effect on the children's growth 
                      in height. | 
                
                These 
                  results, the researchers concluded, show that children have 
                  an improved rate of sustained virological response compared 
                  with reference studies of adult chronic C patients treated with 
                  similar regimens.
                  
                  Investigator affiliations: Université Catholique de 
                  Louvain, Cliniques universitaires St Luc, Bruxelles, Belgium; 
                  Paediatric Gastroenterology, Hospital de clinicas de Porto Alegre, 
                  Porto Alegre, Brazil; Unidade de Hepatologica Pediatrica, Hospital 
                  das clinicas da faculdade de medicina da universidade de Sao 
                  Paulo, Sao Paulo, Brazil; Department of Pediatrics, Stradin 
                  University, Riga, Latvia; Department of Paediatrics, CLINTEC, 
                  Karolinska University Hospital, Huddinge, Stockholm, Sweden; 
                  Liver Unit, Birmingham Children's Hospital, Birmingham, UK.
                  
                  8/31/10
                Reference
                  EM 
                  Sokal, A Bourgois, X Stéphenne, and others. Peginterferon 
                  alfa-2a plus ribavirin for chronic hepatitis C virus infection 
                  in children and adolescents. Journal of Hepatology 52(6): 
                  827-831 (Abstract). 
                  June 2010.