Table 3.
Association guidelines | HBV screening | Screening tests | HBsAg positive patients | HBsAg negative, anti-HBc positive patients | Antiviral drug recommended | Duration of antiviral therapy |
EASL 2012[91] | All candidates for chemo- and immunosuppressive therapy | HBsAg, anti-HBc, HBV DNA if serology positive | Prophylactic antiviral therapy, test for HBV-DNA level | Test for HBV DNA; provide prophylactic antiviral therapy if detectable HBV DNA; monitor ALT and HBV DNA levels closely if no detectable HBV DNA | Lamivudine if HBV DNA < 2000 IU/mL and the treatment duration is finite and short, Entecavir or tenofovir if HBV DNA is high, and/or lengthy and repeated cycles of immunosuppression | 12 mo after cessation of therapy |
APASLD 2012[92] | All patients prior to receiving immunosuppression or chemotherapy | HBsAg, anti-HBc | Prophylactic antiviral therapy | Monitor HBV-DNA | Lamivudine or entecavir or tenofovir | Continue until 6 mo after end of chemotherapy |
AGA 2015[49] | High risk of HBV reactivation (> 10%) and moderate risk of HBV reactivation (1%-10%) | HBsAg, anti-HBc , HBV DNA if serology positive | Prophylactic antiviral therapy | Antiviral prophylaxis over monitoring for patients if the chemotherapy is associated with high or moderate risk of HBV reactivation | Drug with high barrier to resistance is favored over lamivudine | 6 mo after discontinuation of therapy and at least 12 mo for B-cell depleting agents |
Routine screening not recommended for low risk of HBV reactivation (< 1%) | ||||||
AASLD 2009[93], no update in the version in 2016[126] | Anyone at high risk of HBV infection | HBsAg and anti-HBc | Prophylactic antiviral therapy | No recommendation | Lamivudine or telbivudine if the anticipated treatment duration is < 12 mo and baseline HBV DNA is not detectable | Maintain for 6 mo after completion of chemotherapy |
Tenofovir or entecavir if anticipated treatment duration > 12 mo | ||||||
ASCO 2015[94] | Risk-adapted HBV screening strategy | HBsAg, anti-HBc , HBV DNA if serology positive | Prophylactic antiviral therapy | Consider | Entecavir, tenofovir | Minimum of 6 mo after stopping therapy, longer than 12 mo for patients receiving anti-CD20 monoclonal antibodies |
Antiviral prophylaxis if the systemic cancer therapy is associated with high risk of HBV reactivation |
HBV: Hepatitis B virus; EASL: European Association for the Study of the Liver; APASLD: Asian Pacific Association for the Study of the Liver; AGA: American Gastroenterology Association; AASLD: American Association for the Study of Liver Diseases; ASCO: American Society of Clinical Oncology.