Review 
                      Finds Pegylated Interferon Is More Effective than Lamivudine 
                      for Chronic Hepatitis B, but Study Shows Little Activity 
                      against HBV Genotype D
                    
                      
                       
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                              | SUMMARY: 
                                A systemic review of clinical trials found that 
                                pegylated interferon was more effective than the 
                                oral antiviral drug lamivudine 
                                (Epivir-HBV) at achieving endpoints including 
                                hepatitis B virus (HBV) DNA clearance and hepatitis 
                                B "e" antigen (HBeAg) seroconversion, 
                                investigators reported at the 60th Annual Meeting 
                                of the American Association for the Study of Liver 
                                Diseases (AASLD 2009) 
                                this month in Boston. Another study, however, 
                                showed that pegylated 
                                interferon did not work so well against HBV 
                                genotype D. |  |  |  | 
                       
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                    By 
                    Liz Highleyman
                     
                    Two 
                      types of treatment are approved for chronic 
                      hepatitis B, directly targeted oral antiviral agents 
                      such as lamivudine (Epivir-HBV), and conventional or pegylated 
                      interferon, which stimulates immune response to HBV.
                    K. 
                      Mumtaz from Aga Khan University in Pakistan and colleagues 
                      performed a Cochrane review of pegylated interferon for 
                      chronic hepatitis B in adult patients. The Cochrane Collaboration 
                      is an independent network of experts that produces systematic 
                      reviews of healthcare interventions and promotes evidence-based 
                      medicine.
                    The 
                      investigators searched the Cochrane Hepato-Biliary Group 
                      Controlled Trials Register, the Cochrane Central Register 
                      of Controlled Trials, and the MEDLINE, EMBASE, and LILACS 
                      databases for studies published through January 2009 that 
                      compared pegylated interferon versus other therapies for 
                      adult chronic hepatitis B patients.
                    Results
                    
                       
                        |  | The 
                          researchers identified 7 trials reported in 15 publications, 
                          with a total of 2179 participants. | 
                       
                        |  | These 
                          studies showed evidence that pegylated interferon is 
                          superior to lamivudine in achieving outcomes including: | 
                       
                        |  | 
                             
                              |  | HBV 
                                DNA clearance: rate ratio (RR) 0.94; |   
                              |  | HBV 
                                DNA suppression: RR 0.85; |   
                              |  | HBeAg 
                                seroconversion: RR 0.84; |   
                              |  | Hepatitis 
                                B surface antigen (HBsAg) loss: RR 0.97. |  | 
                       
                        |  | Adding 
                          lamivudine to pegylated interferon did not decrease 
                          the "number needed to treat" in order to produce 
                          a successful outcome. | 
                       
                        |  | However, 
                          adverse events were more common with pegylated interferon 
                          than with lamivudine. | 
                    
                    Based 
                      on these findings, the researchers concluded, "Current 
                      evidence suggests that pegylated interferon is better than 
                      lamivudine when used alone or with lamivudine."
                    HBV 
                      Genotype D
                    According 
                      to a related study reported at the same conference, however, 
                      pegylated interferon is not very effective against chronic 
                      HBV genotype D infection.
                    O. 
                      Kurdas and colleagues from Turkey -- where genotype D is 
                      the most common form of HBV, accounting for 97% of cases 
                      -- evaluated the efficacy of pegylated interferon in eligible 
                      chronic hepatitis B patients treated at Haydarpasa Numune 
                      Education and Research Hospital between 2004 and 2007.
                    Eligible 
                      patients met any 2 of the following criteria: less than 
                      60 years of age, ALT > 2 x upper limit of normal, 
                      HBV DNA < 1 million copies/mL, or fibrosis stage 
                      < 3. Patients with initial HBV DNA levels > 
                      1 million copies/mL were pretreated with lamivudine until 
                      their viral load fell below this level, at which point they 
                      could start pegylated interferon.
                    A 
                      total of 28 patients (15 HBeAg positive and 13 HBeAg negative) 
                      were enrolled in the study and treated with 180 mcg/week 
                      pegylated interferon 
                      alfa-2a (Pegasys) or 1.5 mcg/kg/week pegylated 
                      interferon alfa-2b (PegIntron) for 48 weeks. Participants 
                      were followed for an average of 115 weeks after the end 
                      of therapy. 
                    By 
                      week 12, 40% of HBeAg positive patients and 70% of HBeAg 
                      negative patients experienced at least a 2 log reduction 
                      in HBV viral load. At the end of treatment, 39% and 67%, 
                      respectively, had undetectable HBV DNA. However, only 3 
                      HBeAg negative patients and none of the HBeAg positive participants 
                      achieved sustained virological response after completing 
                      therapy. Because of the small numbers, the differences between 
                      the HBeAg positive and HBeAg negative groups were not statistically 
                      significant. Overall, 10 patients (63%) achieved HBeAg seroconversion, 
                      but none achieved HBsAg seroconversion. 
                    These 
                      findings led the investigators to conclude that, "Pegylated 
                      interferon therapy was found ineffective in patients with 
                      chronic hepatitis B genotype D despite young age, high ALT, 
                      low viral load, and low fibrosis scores."
                    11/17/09
                    References
                    K 
                      Mumtaz, S Hamid, and SM Jafri. Pegylated interferon for 
                      chronic hepatitis B in adults: a Cochrane Review. 60th Annual 
                      Meeting of the American Association for the Study of Liver 
                      Diseases (AASLD 2009). Boston. October 30-November 1, 2009. 
                      Abstract 469.
                    O 
                      Kurdas, F Guzelbulut, Y Gökden, and others. PegIFNs 
                      are not satisfactory in genotype D chronic HBV infection. 
                      60th Annual Meeting of the American Association for the 
                      Study of Liver Diseases (AASLD 2009). Boston. October 30-November 
                      1, 2009. Abstract 462.