Background
Data on incidence of adverse liver outcomes is limited for cancer
patients with chronic (HBsAg+/anti-HBc+) or past
(HBsAg−/anti-HBc+) hepatitis B virus (HBV) after
chemotherapy. We aimed to determine the impact of test timing and anti-HBV
therapy on adverse liver outcomes in these patients.
Methods
We retrospectively studied patients with solid or hematologic
malignancies who received chemotherapy during 2004–2011. We defined
HBV testing and anti-HBV therapy to be early at initiation
of cancer therapy and late after initiation. Outcomes
included hepatitis flares, hepatic impairment, liver failure, and death.
Time-to-event analysis was used to determine incidence, and multivariable
hazard models to determine predictors of outcomes.
Results
There were 18,688 study patients (80.4% solid tumors).
Prevalence of chronic HBV was 1.1% (52/4905) and past HBV was
7.1% (350/4905). Among solid tumor patients, late identification of
chronic HBV was associated with higher risk of hepatitis flare, hepatic
impairment, liver failure, and death compared with early identification
[HR (95% CI), 4.02 (1.26–12.86), 8.48
(1.86–38.66), 9.38 (1.50–58.86), and 3.90
(1.19–12.83), respectively]. Among patients with hematologic
malignancies and chronic HBV, risk of death was 7.8 (1.73–35.27)
times higher in persons with late compared to early anti-HBV therapy
initiation. Patients with late identification of chronic HBV had late/no
anti-HBV therapy. Chronic HBV predicted liver failure in patients with solid
or hematologic malignancies while male sex and late identification were
predictors for solid tumor patients.
Conclusion
Early identification correlates with early anti-HBV therapy and
reduces the risk of liver failure and death in chronic HBV patients
receiving chemotherapy.