Outcome of untreated low-level viremia versus antiviral therapy-induced or spontaneous undetectable HBV-DNA in compensated cirrhosis

Author:

Huang Daniel Q.12ORCID,Tamaki Nobuharu3ORCID,Lee Hyung Woong4ORCID,Park Soo Young5ORCID,Lee Yu Rim5ORCID,Lee Hye Won4ORCID,Lim Seng Gee12ORCID,Lim Tae Seop4ORCID,Kurosaki Masayuki3ORCID,Marusawa Hiroyuki6ORCID,Mashiba Toshie7ORCID,Kondo Masahiko8ORCID,Uchida Yasushi9ORCID,Kobashi Haruhiko10ORCID,Furuta Koichiro11,Izumi Namiki3ORCID,Kim Beom Kyung4ORCID,Sinn Dong Hyun12ORCID

Affiliation:

1. Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore

2. Division of Gastroenterology and Hepatology, National University Hospital, Singapore

3. Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan

4. Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea

5. Department of Internal Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea

6. Department of Gastroenterology and Hepatology, Osaka Red Cross Hospital, Osaka, Japan

7. Center for Liver-Biliary-Pancreatic Disease, Matsuyama Red Cross Hospital, Matsuyama, Ehime, Japan

8. Department of Gastroenterology, Japanese Red Cross Otsu Hospital, Otsu, Shiga, Japan

9. Department of Gastroenterology, Matsue Red Cross Hospital, Matsue, Shimane, Japan

10. Department of Gastroenterology, Japanese Red Cross Okayama Hospital, Okayama, Okayama, Japan

11. Department of Gastroenterology, Masuda Red Cross Hospital, Masuda, Shimane, Japan

12. Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea

Abstract

Background: Comparative outcomes of HBV-infected compensated cirrhosis with low-level viremia (LLV) versus maintained virological response (MVR) are unclear. We conducted a large, multiethnic, multicenter study to examine the natural history of LLV versus MVR in compensated cirrhosis. Patients and Methods: We enrolled patients with HBV-infected compensated cirrhosis (n=2316) from 19 hospitals in South Korea, Singapore, and Japan. We defined the LLV group as untreated patients with ≥1 detectable serum HBV-DNA (20–2000 IU/mL), Spontaneous-MVR group as untreated patients with spontaneously achieved MVR, and antiviral therapy (AVT)-MVR group as patients achieving AVT-induced MVR. Study end points were HCC or hepatic decompensation. Results: The annual HCC incidence was 2.7/100 person-years (PYs), 2.6/100 PYs, and 3.3/100 PYs for LLV (n=742), Spontaneous-MVR (n=333), and AVT-MVR (n=1241) groups, respectively (p = 0.81 between LLV vs. Spontaneous-MVR groups and p = 0.37 between LLV vs. AVT-MVR groups). Similarly, the annual decompensation incidence was 1.6/100 PYs, 1.9/100 PYs, and 1.6/100 PYs for LLV, Spontaneous-MVR, and AVT-MVR groups, respectively (p = 0.40 between LLV vs. Spontaneous-MVR groups and p = 0.83 between LLV vs. AVT-MVR groups). Multivariable analyses determined that HCC and decompensation risks in the LLV group were comparable to those with Spontaneous-MVR and AVT-MVR groups (all p >0.05). Propensity score matching also reproduced similar results for HCC and decompensation risks (all p>0.05 between LLV vs. Spontaneous-MVR groups and between LLV vs. AVT-MVR groups). Conclusions: Untreated LLV in HBV-infected compensated cirrhosis is not associated with increased risk of disease progression compared with Spontaneous-MVR and AVT-MVR. These data have important implications for practice and further research.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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