Although
antiviral prophylaxis is essential in
hepatitis B patients in the context of
cancer chemotherapy, there is little evidence-based consensus regarding the appropriate prevention strategy depending on the underlying type of
cancer and viral status. This retrospective study included a comprehensive cohort of 302
hepatitis B surface antigen-positive patients with various
cancers undergoing
chemotherapy and
antiviral prophylaxis. The rates of hepatitis B virus (HBV) reactivation during
antiviral therapy (>1 log10 IU/mL increase or positive conversion of serum HBV
DNA) and relapse when off
antivirals ([re]appearance of HBV DNA >2,000 IU/ml with related
alanine aminotransferase elevation) were evaluated, together with the associated risk factors, in a competing risks analysis where
cancer death was considered as the competing event. During
antiviral prophylaxis, HBV was reactivated in six patients (1.9%), who had
leukemia (n = 4) or
lymphoma (n = 2) and were treated with
lamivudine (n = 4) or
entecavir (n = 2). The incidence rate of HBV relapse in 127 off-prophylaxis patients was 21.3% during a median post-
antiviral period of 11.7 months.
Lymphoma, pre-prophylactic HBV
DNA ≥2,000 IU/ml, and age ≥50 years were independent predictors of off-treatment HBV relapse (adjusted hazard ratios 5.25, 3.07, and 0.34, respectively; Ps < 0.05).
Antiviral and anticancer drugs, duration of consolidation on
antiviral prophylaxis, and
HBeAg positivity were not independent predictors. In conclusion,
hepatitis B flare-ups are not rare in patients receiving
cancer chemotherapy during and after anti-HBV prophylaxis, even when potent
antivirals are used. Patients with hematopoietic or lymphoid
neoplasms or high viral burdens should receive prolonged and powerful HBV prophylaxis. J. Med. Virol. 88:1576-1586, 2016. © 2016 Wiley Periodicals, Inc.