中文版 | English
Title

Early clinical efficacy of pegylated interferon treatment in patients with different phases of chronic HBV infection: A real-world analysis

Author
Corresponding AuthorSong, Jianxin; Li, Guojun
Publication Years
2023-05-01
DOI
Source Title
ISSN
1352-0504
EISSN
1365-2893
Volume30Issue:5
Abstract
Although there are therapeutic advantages for hepatitis B virus (HBV) withpegylated interferon alpha (peg-IFN alpha) treatment compared with nucleos(t)ide analog (NAs) therapy, the effect difference in infected population at different phases has not been well established. We studied the clinical efficacy of peg-IFN alpha in two populations with HBV infection, including inactive HBsAg carrier (IHC) and chronic hepatitis B (CHB). A total of 328 HBV-infected patients were included in this real-world analysis. Patients were divided into two groups according to the infected stages. Peg-IFN alpha monotherapy or combination therapy with NAs were used in IHCs, and peg-IFN alpha added-on NAs therapy was applied to patients with CHB. The primary efficacy endpoint was HBsAg loss at Week 24. Results: The Kaplan-Meier cumulative rates of HBsAg loss were 39.50% (n = 47/119) in IHC group and 28.71% (n = 60/209) in CHB group at Week 24 (p < .05). After Propensity Score Matching (PSM), the HBsAg loss rates were 36.84% (n = 35/95) and 32.63% (n = 31/95), respectively (p > .05). Patients with baseline HBsAg level < 100 IU/ml achieved higher rates of HBsAg clearance in IHC and CHB group (before PSM: 47.44% vs. 42.86%, after PSM: 49.12% vs. 45.83%, all p values > .05). Baseline HBsAg level and its level decline from baseline to Week 12 can be as the predictors for HBsAg loss at Week 24 in both groups. Hence, the efficacy of HBsAg clearance was broadly similar between IHCs and NA-treated CHB patients during the early peg-IFN alpha therapy. A significant downward trend of HBsAg level was observed in both groups during peg-IFN alpha therapy.
Keywords
URL[Source Record]
Indexed By
Language
English
SUSTech Authorship
Corresponding
Funding Project
null[JCYJ20190812151601664] ; null[2016KYA162] ; null[2020076]
WOS Research Area
Gastroenterology & Hepatology ; Infectious Diseases ; Virology
WOS Subject
Gastroenterology & Hepatology ; Infectious Diseases ; Virology
WOS Accession No
WOS:000907909700001
Publisher
ESI Research Field
IMMUNOLOGY
Data Source
Web of Science
Citation statistics
Cited Times [WOS]:1
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/583157
DepartmentThe Third People's Hospital of Shenzhen
南方科技大学第一附属医院
Affiliation
1.Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Infect Dis, Wuhan, Peoples R China
2.Ezhou Cent Hosp, Dept Infect Dis, Ezhou, Peoples R China
3.Southern Univ Sci & Technol, Shenzhen Peoples Hosp 3, Affiliated Hosp 2, Natl Clin Res Ctr Infect Dis,Dept Liver Dis,State, Shenzhen, Peoples R China
4.Peoples Hosp Longhua, Dept Infect Dis, Shenzhen, Peoples R China
5.Shenzhen Third Peoples Hosp, Dept Liver Dis, 29 Bulan Rd, Shenzhen 518112, Peoples R China
6.Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Infect Dis, 1095 Jiefang Ave, Wuhan 430030, Peoples R China
Corresponding Author AffilicationThe Third People's Hospital of Shenzhen;  Shenzhen People's Hospital
First Author's First AffilicationThe Third People's Hospital of Shenzhen;  Shenzhen People's Hospital
Recommended Citation
GB/T 7714
Zhang, Wencong,Xing, Mingyou,Sun, Wenjin,et al. Early clinical efficacy of pegylated interferon treatment in patients with different phases of chronic HBV infection: A real-world analysis[J]. JOURNAL OF VIRAL HEPATITIS,2023,30(5).
APA
Zhang, Wencong.,Xing, Mingyou.,Sun, Wenjin.,Chen, Jia.,Xie, Nana.,...&Li, Guojun.(2023).Early clinical efficacy of pegylated interferon treatment in patients with different phases of chronic HBV infection: A real-world analysis.JOURNAL OF VIRAL HEPATITIS,30(5).
MLA
Zhang, Wencong,et al."Early clinical efficacy of pegylated interferon treatment in patients with different phases of chronic HBV infection: A real-world analysis".JOURNAL OF VIRAL HEPATITIS 30.5(2023).
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