Recommendations for Hepatitis B Virus (HBV) Screening and Management
All patients with cancer anticipating systemic anticancer therapy should be screened for HBV with three tests—hepatitis B surface antigen (HBsAg), hepatitis B core antibody (anti-HBc), and antibody to hepatitis B surface antigen (anti-HBs)—prior to starting treatment. 1
Screening Recommendations
Who Should Be Screened for HBV
Universal screening for specific populations:
Risk-based screening:
- Persons at moderate or high risk who will undergo immunosuppressive drug therapy 1
- Persons with HIV infection 1
- Persons who inject drugs 1, 3
- Men who have sex with men 3
- Household contacts of HBV-infected persons 3
- Persons from countries with high HBV prevalence 3
- Persons with a history of sexually transmitted infections or multiple sex partners 4
- Persons with history of hepatitis C virus infection 4
- Persons with incarceration history 4
Additional considerations:
Recommended Screening Tests
Complete screening panel includes:
- Hepatitis B surface antigen (HBsAg)
- Hepatitis B core antibody (anti-HBc) total or IgG
- Antibody to hepatitis B surface antigen (anti-HBs) 1
Follow-up testing:
- If either HBsAg or anti-HBc is positive, perform a sensitive HBV DNA test 1
Interpretation of HBV Test Results
| HBV Status | HBsAg | Anti-HBc | Anti-HBs |
|---|---|---|---|
| Chronic HBV infection | Positive | Positive | Negative |
| Past HBV infection (resolved) | Negative | Positive | Positive |
| Isolated core antibody | Negative | Positive | Negative |
Management of HBV-Infected Patients
Chronic HBV Infection (HBsAg-positive)
For patients receiving any systemic anticancer therapy:
- Initiate antiviral prophylaxis before starting immunosuppressive therapy 1
- Continue antiviral therapy for the duration of anticancer therapy plus at least 12 months after completion 1
- Monitor ALT and HBV DNA at baseline and every 6 months during antiviral therapy 1
- After stopping antivirals, monitor ALT monthly for 3 months, then every 3 months thereafter 1
For patients receiving immunosuppressive therapy:
Past HBV Infection (HBsAg-negative, anti-HBc-positive)
For patients receiving high-risk therapies (e.g., anti-CD20 monoclonal antibodies, stem-cell transplantation):
- Initiate antiviral prophylaxis at the beginning of anticancer therapy 1
- Continue for at least 12 months after completion of therapy 1
- Monitor HBV DNA every 6 months during antiviral therapy 1
- Alternative approach: Monitor HBsAg and HBV DNA every 3 months and start antivirals at earliest sign of reactivation 1
For patients receiving lower-risk anticancer therapies:
Antiviral Medication Selection
Preferred agents (high genetic barrier to resistance):
Not recommended:
- Lamivudine (due to high resistance rates of 20-30%) 1
Special Considerations
- Hormonal therapy alone is unlikely to increase risk of HBV reactivation 1
- Renal function monitoring is essential with tenofovir use due to potential nephrotoxicity 6
- Cost-effectiveness: HBV screening is cost-effective even when prevalence is as low as 0.3% 1
Common Pitfalls to Avoid
Delaying anticancer therapy for HBV screening results - Anticancer therapy should not be delayed while awaiting screening test results 1
Using lamivudine for prophylaxis - High resistance rates make this a suboptimal choice; use entecavir or tenofovir instead 1
Discontinuing monitoring too early - Delayed HBV reactivation can occur years after cessation of anticancer therapy 1
Missing high-risk patients - Universal screening for cancer patients is more effective than risk-based screening, which may miss cases 1
Inadequate duration of prophylaxis - Continue antivirals for at least 12 months after completing anticancer therapy 1