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GS02
FIVE-YEAR ON-TREATMENT SYSTEMATICALLY MONITORING OF
DYNAMIC CHANGES OF LIVER STIFFNESS MEASUREMENT WITH
TRANSIENT ELASTOGRAPHY COMPARED WITH PAIRED LIVER
BIOPSIES IN A RANDOMIZED CONTROLLED TRIAL IN CHRONIC
HEPATITIS B PATIENTS
J. Sun1, Q. Xie2, D. Tan3, Q. Ning4, J. Niu5, X. Bai6, R. Fan1, X. Liang1,
S. Chen7, J. Cheng8, Y. Yu9, H. Wang10, M. Xu11, G. Shi12, M.Wan13,
X. Chen14, H. Tang15, J. Sheng16, X. Dou17, J. Shi18, H. Ren19, M.Wang20,
H. Zhang21, Z. Gao22, C. Chen23, H. Ma24, Y. Chen1, J. Jia24, J. Hou1.
1Hepatology Unit, Nanfang Hospital, Southern Medical University,
Guangzhou; 2Department of Infectious Diseases, Ruijin Hospital,
Shanghai; 3Department of Infectious Diseases, Xiangya Hospital,
Changsha; 4Department of Infectious Diseases, Tongji Hospital, Wuhan;
5Hepatology Unit, No.1 Hospital affiliated to Jilin University, Changchun;
6Department of Infectious Diseases, Tangdu Hospital, Xi’an; 7Ji’nan
Infectious Diseases Hospital, Ji’nan; 8Beijing Ditan Hospital;
9Department of Infectious Diseases, First Hospital of Peking University;
10Hepatology Unit, Peking University People’s Hospital, Beijing;
118th People’s Hospital, Guangzhou; 12Department of Infectious Diseases,
Huashan Hospital; 13Department of Infectious Diseases, Changhai
Hospital, Shanghai; 14Beijing Youan Hospital, Beijing; 15Department of
Infectious Diseases, Huaxi Hospital, Chengdu; 16Department of
Infectious Diseases, Zhejiang University 1st Affiliated Hospital,
Hangzhou; 17Department of Infectious Diseases, Shengjing Hospital,
Shenyang; 186th People’s Hospital, Hangzhou; 19Department of
Infectious Diseases, Chongqing Medical University 2nd Affiliated
Hospital, Chongqing; 20Department of Infectious Diseases, 81st PLA
Hospital, Nanjing; 21302nd PLA Hospital, Beijing; 22Department of
Infectious Diseases, Sun Yat-Sen University 3rd Affiliated Hospital,
Guangzhou; 23Department of Infectious Diseases, 85th PLA Hospital,
Shanghai; 24Hepatology Unit, Beijing Friendship Hospital, Beijing, China
E-mail: [email protected]
Background and Aims: Transient elastography is a rapid, noninvasive
and reproducible method to measure liver stiffness. Liver
stiffness measurement (LSM) has been shown to be a reliable tool
to diagnose advanced fibrosis or liver cirrhosis in chronic hepatitis B
(CHB). However, the use of LSM to monitor liver fibrosis dynamics
has not been thoroughly evaluated during antiviral therapy.
Methods: Six hundred and six patients with HBV DNA ≥5 Log10
copies/mL, ALT 2–10 × ULN and compensated adult naive HBeAgpositive
CHB were enrolled in a multicenter, randomized controlled
trial (EFFORT Study; Sun J, et al. Hepatology. 2014; Fan R, et al. Gut.
2015), receiving telbivudine (LDT) alone or combined with adefovir
(ADV) for up to 260 weeks (5 years). LSM was performed using
transient elastography (FibroScan®, Echosens, France) at the interval
of 24weeks during the 5-year antiviral treatment. Percutaneous liver
biopsy was performed at baseline and week 104.
Results: Five hundred and ninety-nine of intent-to-treat population
were enrolled in the analysis, among which 347 patients with
qualified paired biopsies. During 5-year antiviral treatment, LSM
decreased rapidly from 8.5 (2.6–49.5) kPa at baseline to 6.1 (2.2–37.4)
kPa at week 24, and then decreased slowly from 6.1 (2.2–37.4) kPa at
week 24–4.9 (2.3–19.6) kPa at week 260. From baseline toweek 104,
liver biopsy evaluation showed that the proportion of patients with
no or mild necroinflammation (Knodell range 0–3) increased from
29.7% (103/347) to 77.2% (268/347), and the proportion of patients
with no or mild fibrosis (Ishak range 0–2) increased from 29.1%
(101/347) to 66.0% (229/347). At baseline, the AUROC of LSM for
patients with advanced fibrosis (Ishak >2) was 0.816. Multivariate
logistic regression analysis showed that values of 24-week and 52-
week LSM were independently associated with 104-week liver
necroinflammation (Knodell ≤2; OR, 1.889; p = 0.014) and fibrosis
(Ishak ≤2; OR, 3.002; p = 0.023), respectively.
Conclusions: The kinetics of LSM decreased during long-term
antiviral therapy with bi-phase pattern, which may mainly reflect
the resolution of inflammation during the first phase, and the
regression of fibrosis during the second phase. Transient elastography
is a useful tool for the evaluation of the change of liver inflammation
and fibrosis during antiviral therapy.
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