TY - JOUR
T1 - APASL HCV guidelines of virus-eradicated patients by DAA on how to monitor HCC occurrence and HBV reactivation
AU - Kanda, Tatsuo
AU - Lau, George K.K.
AU - Wei, Lai
AU - Moriyama, Mitsuhiko
AU - Yu, Ming Lung
AU - Chuang, Wang Long
AU - Ibrahim, Alaaeldin
AU - Lesmana, Cosmas Rinaldi Adithya
AU - Sollano, Jose
AU - Kumar, Manoj
AU - Jindal, Ankur
AU - Sharma, Barjesh Chander
AU - Hamid, Saeed S.
AU - Kadir Dokmeci, A.
AU - Mamun-Al-Mahtab,
AU - McCaughan, Geoffrey W.
AU - Wasim, Jafri
AU - Crawford, Darrell H.G.
AU - Kao, Jia Horng
AU - Ooka, Yoshihiko
AU - Yokosuka, Osamu
AU - Sarin, Shiv Kumar
AU - Omata, Masao
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2019/11/1
Y1 - 2019/11/1
N2 - In the direct-acting antiviral (DAA) era for hepatitis C virus (HCV) infection, sustained virological response (SVR) is very high, but close attention must be paid to the possible occurrence of hepatocellular carcinoma (HCC) and reactivation of hepatitis B virus (HBV) in patients with co-infection who achieved SVR in short term. HCC occurrence was more often observed in patients with previous HCC history. We found occurrence of HCC in 178 (29.6%) of 602 patients with previous HCC history (15.4 months mean follow-up post-DAA initiation) but, in contrast, in only 604 (1.3%) of 45,870 patients without previous HCC history (18.2 months mean follow-up). Thus, in these guidelines, we recommend the following: in patients with previous HCC history, surveillance at 4-month intervals for HCC by ultrasonography (US) and tumor markers should be performed. In patients without previous HCC history, surveillance at 6- to 12-month intervals for HCC including US is recommended until the long-term DAA treatment effects, especially for the resolution of liver fibrosis, are confirmed. This guideline also includes recommendations on how to follow-up patients who have been infected with both HCV and HBV. When HCV was eradicated in these HBsAg-positive patients or patients with previous HBV infection (anti-HBc and/or anti-HBs-positive), it was shown that HBV reactivation or HBV DNA reappearance was observed in 67 (41.4%) of 162 or 12 (0.9%) of 1317, respectively. For these co-infected patients, careful attention should be paid to HBV reactivation for 24 weeks post-treatment.
AB - In the direct-acting antiviral (DAA) era for hepatitis C virus (HCV) infection, sustained virological response (SVR) is very high, but close attention must be paid to the possible occurrence of hepatocellular carcinoma (HCC) and reactivation of hepatitis B virus (HBV) in patients with co-infection who achieved SVR in short term. HCC occurrence was more often observed in patients with previous HCC history. We found occurrence of HCC in 178 (29.6%) of 602 patients with previous HCC history (15.4 months mean follow-up post-DAA initiation) but, in contrast, in only 604 (1.3%) of 45,870 patients without previous HCC history (18.2 months mean follow-up). Thus, in these guidelines, we recommend the following: in patients with previous HCC history, surveillance at 4-month intervals for HCC by ultrasonography (US) and tumor markers should be performed. In patients without previous HCC history, surveillance at 6- to 12-month intervals for HCC including US is recommended until the long-term DAA treatment effects, especially for the resolution of liver fibrosis, are confirmed. This guideline also includes recommendations on how to follow-up patients who have been infected with both HCV and HBV. When HCV was eradicated in these HBsAg-positive patients or patients with previous HBV infection (anti-HBc and/or anti-HBs-positive), it was shown that HBV reactivation or HBV DNA reappearance was observed in 67 (41.4%) of 162 or 12 (0.9%) of 1317, respectively. For these co-infected patients, careful attention should be paid to HBV reactivation for 24 weeks post-treatment.
KW - DAA
KW - Follow-up
KW - Guideline
KW - HBV
KW - HCC
KW - HCV
KW - SVR
UR - http://www.scopus.com/inward/record.url?scp=85074431342&partnerID=8YFLogxK
U2 - 10.1007/s12072-019-09988-7
DO - 10.1007/s12072-019-09988-7
M3 - Article
C2 - 31541423
AN - SCOPUS:85074431342
SN - 1936-0533
VL - 13
SP - 649
EP - 661
JO - Hepatology International
JF - Hepatology International
IS - 6
ER -