Hepatitis B Research Network Pediatric Cohort Study (HBRN)

Completed

• Conditions: Hepatitis B

• Registration Number: NCT01263600
• Lead Sponsor: University of Pittsburgh

Brief Summary

The purpose of this study is to describe participants 6 months to \<18 years of age with hepatitis B virus (HBV) infection in a prospective cohort in the United States (US) and Canada and identify predictors of disease activation and progression.

Detailed Description

•Primary Aim:

o To describe participants 6 months to \<18 years of age with hepatitis B virus (HBV) infection in a prospective cohort in the United States (US) and Canada and identify predictors of disease activation and progression

Secondary Aims:

* To describe clinical, virological, and immunological characteristics of participants with HBV in the US and Canada.

* To evaluate changes in HBV infection status and hepatitis B surface antigen (HBsAg) levels and factors associated with those changes.

* To verify whether a baseline HBsAg below 1,000 IU/mL and HBV DNA below 1,000 IU/mL is an accurate predictor of people who are, or who will become, inactive carriers, defined as people who are HBsAg positive, hepatitis B "e" antigen (HBeAg) negative, have normal alanine aminotransferase (ALT) and HBV DNA under 1,000 IU/mL on at least two occasions over a period of at least 6 months with HBV DNA under 1,000 IU/mL.

* To assess the health related quality of life (HRQOL) of treatment naïve hepatitis B surface antigen (HBsAg) positive children and adolescents

* To develop a bank of biospecimens (e.g., serum, plasma, DNA, liver tissue) obtained from participants with HBV infection.

* To identify pediatric participants from 2 years to \<18 years of age with chronic HBV infection for potential participation in treatment study to be conducted by the Hepatitis B Research Network (HBRN).

Study Timeline

• Study Start: 2010-12
• Study First Submitted: 2010-12-14
• Study First Submitted QC: 2010-12-17
• Study First Posted: 2010-12-20
• Primary Completion: 2021-06-09
• Study Completion: 2021-06-09
• Status Verified: 2022-05
• Last Update Submitted: 2022-05-26
• Last Update Posted: 2022-05-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 462

Inclusion Criteria

• Written informed consent/assent as appropriate
• At least 6 months to <18 years of age
• Hepatitis B surface antigen (HBsAg) positive

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Exclusion Criteria

• Hepatic decompensation
• Hepatocellular carcinoma (HCC)
• Liver transplantation
• Current Hepatitis B antiviral treatment (except pregnant females)
• Known coinfection with HIV (patients with hepatitis D or hepatitis C coinfection are not excluded)
• Medical or social condition which in the opinion of the principal investigator would interfere with or prevent regular follow up.
• Unable or unwilling to return for regular follow-up

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Antigen loss: e and s	up to 288 weeks	Loss of these viral markers may be associated with appearance of corresponding antibodies in serum (anti-HBe or anti-HBs). HBsAg loss appears to represent a "cure" of HBV infection and is associated with reduction, but not necessarily elimination, of the risk of future complications, such as Hepatocellular carcinoma (HCC) which may occur, particularly in those who lose HBsAg at an older age (after 50 years) or after the development of cirrhosis. When HBeAg or HBsAg loss occurs, participants will be followed more closely initially and then return to the regular follow-up schedule.

Secondary Outcome Measures

Name	Time	Method
Cirrhosis	up to 288 weeks	The diagnosis of cirrhosis will be made by (1) liver histology, when available or In the absence of histological diagnosis, cirrhosis is defined as any one of the following; * Presence of ascites or hepatic hydrothorax; * Variceal or portal hypertensive bleeding; * Hepatic encephalopathy; * Child-Turcotte-Pugh (CTP) score of 7 or above; or in the absence of hepatic decompensation (any two of the following): * Splenomegaly; * Nodular liver; * Platelet count below 120,000/mm3; Once cirrhosis is diagnosed, patient follow-up should include Hepatocellular carcinoma(HCC)surveillance
Reaching 18 years of Age	up to 288 weeks	Patients who reach 18 years of age and are within an adult HBRN clinical center will be offered participation in the adult cohort study and re-consented for the adult protocol.
Hepatitis exacerbation marked by alanine aminotransferase (ALT) Flare	up to 288 weeks	A flare is defined as serum alanine aminotransferase (ALT) greater than or equal to 10 times the upper limit of normal which corresponds to (1 550 IU/L in females and 600 IU/L in males for 6 months - 18 months of age and 2) 350 IU/L in females and 400 IU/L in males for \>18 months - \< 18 years of age (12). Once a flare is detected, participants will be followed more closely until its resolution.
Hepatocellular carcinoma (HCC)	up to 288 weeks	HCC may be detected by routine surveillance or may become clinically apparent. The diagnosis of HCC will be made using the American Association for the Study of Liver Disease criteria.
Liver transplantation	up to 288 weeks	Liver transplantation will be recorded upon notification. Date of transplantation, indication for transplantation, and occurrence of incidental HCC will be recorded. Follow-up ends with liver transplantation.
Hepatic Decompensation	up to 288 weeks	It is likely that the development of cirrhosis and subsequent hepatic decompensation will be preceded and foreseen by the progression of fibrosis. Development of hepatic decompensation will be defined by any of the following events: * Ascites or hepatic hydrothorax; * Variceal bleeding or portal hypertensive bleeding; * Hepatic encephalopathy; * Child-Turcotte-Pugh (CTP) score of 7 or above; It is anticipated that there will be a small number of patients that will develop decompensation during the follow-up.
Death	up to 288 weeks	Death may occur related to liver disease (typically hepatic decompensation or HCC) or may occur unrelated to hepatitis B or liver disease. Date and cause of death will be recorded.

Trial Locations

Locations (7)

Johns Hopkins University; 🇺🇸 Baltimore, Maryland, United States

Seattle Children's Hospital; 🇺🇸 Seattle, Washington, United States

Cardinal Glennon Children's Medical Center; 🇺🇸 Saint Louis, Missouri, United States

University of California San Francisco Medical Center; 🇺🇸 San Francisco, California, United States

University of Texas Southwestern; 🇺🇸 Dallas, Texas, United States

University of Minnesota; 🇺🇸 Minneapolis, Minnesota, United States

Hospital for Sick Children; 🇨🇦 Toronto, Ontario, Canada