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Hepatitis B Virus Reactivation After Withdrawal of Preemptive Antiviral Therapy in Hematologic Malignancy

Comparison of the Occurrence of HBV Reactivation According to the Duration of Preemptive Antiviral Therapy in Chronic Hepatitis B Virus Carriers Receiving Cancer Chemotherapy for Hematologic Diseases

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02056548
Enrollment
126
Registered
2014-02-06
Start date
2014-03-31
Completion date
2018-12-31
Last updated
2014-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Hepatitis B, Lymphoma

Keywords

preemptive antiviral treatment, lymphoma, chronic hepatitis B

Brief summary

Previous studies dealt with patients who maintained antiviral drugs for 2 \ 6 months after final chemotherapy and they revealed that many of the patients who stopped preemptive antiviral drug within 6 months experienced viral reactivation. Based on the study results, guidelines recommend that preemptive antiviral therapy should be maintained for at least 6 months. Nevertheless, many clinicians apply the preemptive antiviral drugs for 1\ 2 years or longer after final chemotherapy without definite evidences, and this practice increases the medical expenditure a lot. Therefore, the investigators are going to find out the proper and safe duration of preemptive antiviral therapy which can be a good reference in the future practice.

Detailed description

HBV reactivation in cancer patients is important not only for directly affecting severe hepatic failure but also for delaying of the further cancer treatments which may cause reduction of overall survival. Thus the guidelines according to the previous studies and other follow-up of randomized studies revealed that patients with positive HbsAg should be administered with preemptive antiviral therapy at least 6 month or more. However, ideal duration for preemptive antiviral therapy to suppress viral reactivation and withdrawal hepatitis is not clearly identified at present time. It is because previous data just dealt with the efficiency of preemptive antiviral therapy, but most of them did not analyze the outcomes after withdrawal of antiviral therapy. Frequent late-onset reactivation hepatitis in association with preemptive antiviral therapy is mainly due to drug-resistance or post-withdrawal manifestation. Drug-resistance was mainly associated with lamivudine which is now substituted by entecavir or tenofovir which produce lower incidence of resistance (\< 1.2% at 6 years). Therefore, the only issue at present is withdrawal hepatitis which may be due to early cessation of the antiviral drug.

Interventions

None listed

Sponsors

Seoul St. Mary's Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years old or older * ECOG performance status 0, 1, 2 * Hodgkin's or Non-Hodgkins lymphomas according to the WHO 2008 classification * Patients who received standard cytotoxic chemotherapies * Patients who finished chemotherapy (duration not exceeded 6 months) or who will finish the planned chemotherapy * Patients who achieved at least partial response and do not need further chemotherapy * HBsAg (+) patients who received preemptive antiviral therapies

Exclusion criteria

* Anti-HCV Ab(+), HIV(+), or autoimmune hepatitis * Complications due to uncompensated liver cirrhosis * Child pugh score : 10 points or more * Hepatocellular carcinoma * Patients who finish the lymphoma treatments with only radiotherapy

Design outcomes

Primary

MeasureTime frame
Cumulative incidence rate of hepatitis B viral reactivationwithin one year after cessation of the antiviral drug

Secondary

MeasureTime frameDescription
Severity of reactivation of hepatitis Bwithin one year after cessation of anviral drugsSeverity according to ALT (IU/L) level Mild : up to 5 times from upper normal limit Moderate : 5- 10 times from upper normal limit Severe : ALT \> 300 IU/L or ≥ 10 times

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026