Duration of Tenofovir 300mg Treatment for Chronic Hepatitis B
For most patients with chronic hepatitis B, tenofovir 300mg treatment should be continued indefinitely (lifelong), as discontinuation typically leads to virologic relapse unless HBsAg loss occurs. 1
Treatment Duration Based on Disease Characteristics
Patients Requiring Lifelong Therapy
- All patients with decompensated cirrhosis at treatment initiation must receive lifelong antiviral therapy regardless of virologic response 1
- Patients with compensated cirrhosis (F4) or significant fibrosis (F3) at baseline should continue indefinite treatment due to persistent HCC risk and potential for severe hepatitis flares 1
- HBeAg-negative patients generally require long-term (indefinite) treatment because discontinuation without HBsAg loss leads to virologic relapse 1, 2
Potential Stopping Points (Rare)
HBsAg loss with or without seroconversion is the only acceptable endpoint for treatment discontinuation in non-cirrhotic patients 1
HBeAg-positive patients with minimal fibrosis (<F3) who achieve HBeAg seroconversion may consider discontinuation after 6-12 months of consolidation therapy, though long-term therapy is increasingly preferred due to risk of recurrent viremia and ALT flares 1
Expected Treatment Outcomes Over Time
Virologic Response Timeline
- Week 12: Monitor for primary treatment failure (HBV DNA decline <1 log₁₀ IU/mL) 1
- Week 24: Confirm continued viral suppression; 93% should have HBV DNA <400 copies/mL 1
- Year 5: 96-99% achieve HBV DNA <400 copies/mL with continued treatment 1
- Years 7-8: 98-99.6% maintain undetectable HBV DNA 3, 4
Resistance Profile
- No genotypic resistance to tenofovir has been detected through 8-10 years of treatment 1, 3, 4
- Virologic breakthrough is rare and typically due to nonadherence rather than resistance 1
Special Circumstances Requiring Extended Treatment
Immunosuppression or Chemotherapy
- Continue tenofovir prophylaxis throughout the entire duration of immunosuppressive therapy 3
- Extend treatment for at least 12 months after cessation of immunosuppression (24 months for rituximab) 3, 2
HIV Coinfection
- Treatment must be indefinite as part of combination antiretroviral therapy active against both viruses 5
Monitoring During Long-Term Treatment
- HBV DNA: Every 3-6 months during first year, then every 6-12 months 1, 3
- Liver enzymes (ALT/AST): Every 3-6 months 3
- Renal function (creatinine, CrCl): Every 3-12 months depending on risk 3
- Quantitative HBsAg: Annually to assess for potential functional cure 3
- HCC surveillance: Every 6 months for high-risk patients (cirrhosis, Asian men >40, Asian women >50, family history) 3
Critical Pitfalls to Avoid
- Do not discontinue therapy based solely on undetectable HBV DNA without HBsAg loss, as this leads to virologic relapse 1, 2
- Do not attribute virologic breakthrough to resistance first—assess adherence and drug interactions before resistance testing 3
- Do not delay or discontinue HCC surveillance even with complete viral suppression, as risk persists indefinitely 3