Overview

Efficacy and Safety of Peginterferon a-2a in Patients of Chronic Hepatitis B With Spontaneous Decline of HBV DNA

Status:
Completed
Trial end date:
2013-02-01
Target enrollment:
0
Participant gender:
All
Summary
Patients with spontaneous decline of HBV DNA were non-randomly assigned to accept peginterferon alfa-2a or entecavir therapy, or didn't accept any antiviral regiment.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Third Affiliated Hospital, Sun Yat-Sen University
Treatments:
Entecavir
Interferon-alpha
Peginterferon alfa-2a
Criteria
This study focused on the subsequential antiviral therapeutic strategies for chronic
hepatitis B patients with spontaneous decline of HBV DNA after acute exacerbation. Patients
fullfilled the following criterias were chosen for screening: They were antiviral treatment
naı¨ve and had been positive for hepatitis B surface antigen (HBsAg) for at least 6 months,
were positive for HBeAg and had an HBV DNA Level of more than 500,000IU/ml. Their serum
alanine aminotransferase level was greater than 2 but less than or equal to 30 times the
upper limit of the normal range, their peak value of total bililubin ranged from 2mg/ml to
20mg/ml and the prothrombin time activity was greater than 60%.

ALL of these patients were hospitalized and pretreated with anti-inflammation and liver
protection agents such as Stronger Neo-Minophagen C, Polyunsaturated phosphatidylcholine
(Essentiale), Ursodeoxycholic Acid and L-Glutathione reduced, without any nuclutide of
nucleoside. Their ALT、TBIL and PTA were monitor weekly and HBVDNA level were measured every
two weeks. Patients were eligible if their HBVDNA declined spontaneously by 2 log(10) IU/mL
while their ALT falled below 10 ULN and TBIL falled below 2mg/ml within 8 weeks of
pretreatment.

Patients with advanced fibrosis, cirrhosis and hepatoma were excluded. Other cause of
chronic liver disease should be systematically checked to exclude co-infection with HDV,
HCV and HIV, comorbidities with alcoholism, autoimmune and metabolic liver disease. Serious
medical or psychiatric illnesses that had usage of corticosteroid or immunosup-pressive
agents at the time of study were excluded. All patients in this study lived in Guangdong, a
province of 100,000,000 populations, with same demographics. Owing to patients fear or
refusal of liver biopsy, no patients had the liver biopsy and the rest relied on other
clinical methods to obtain equivalent information of patient conditions. In our cases,
ultrasonorgraphy helped to filter out patients with advanced fibrosis.The liver sonar
examination was performed by two experi-enced hepatologists at least three times on each
patient.