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Inverse Propensity Score-Weighted Analysis of Entecavir and Tenofovir Disoproxil Fumarate in Patients with Chronic Hepatitis B: A Large-Scale Multicenter Studyopen access

Authors
Kim, JihyeHur, Moon HaengKim, Seung UpKim, Jin-WookSinn, Dong HyunLee, Hyun WoongKim, Moon YoungCheong, Jae YounJung, Yong JinLee, Han AhJin, Young-JooYoon, Jun SikPark, Sung-JaeLee, Chang HunKim, In HeeLee, June SungCho, Young YounKim, Hyung JoonPark, Soo YoungSeo, Yeon SeokOh, HyunwooJun, Dae WonKim, Mi NaChang, YoungJang, Jae YoungHwang, Sang YounKim, Yoon Jun
Issue Date
May-2023
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
entecavir; tenofovir; liver cancer; extrahepatic malignancy; virologic response
Citation
Cancers, v.15, no.11
Indexed
SCIE
SCOPUS
Journal Title
Cancers
Volume
15
Number
11
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/63478
DOI
10.3390/cancers15112936
ISSN
2072-6694
Abstract
Tenofovir disoproxil fumarate (TDF) is reportedly superior or at least comparable to entecavir (ETV) in preventing hepatocellular carcinoma (HCC) among chronic hepatitis B (CHB) patients; however, it remains controversial. This study aimed to conduct comprehensive comparisons between the two antivirals. CHB patients initially treated with ETV or TDF between 2012 and 2015 at 20 referral centers in Korea were included. The primary outcome was the cumulative incidence of HCC. The secondary outcomes included death or liver transplantation, liver-related outcome, extrahepatic malignancy, development of cirrhosis, decompensation events, complete virologic response (CVR), seroconversion rate, and safety. Baseline characteristics were balanced using the inverse probability of treatment weighting (IPTW). Overall, 4210 patients were enrolled: 1019 received ETV and 3191 received TDF. During the median follow-ups of 5.6 and 5.5 years, 86 and 232 cases of HCC were confirmed in the ETV and TDF groups, respectively. There was no difference in HCC incidence between the groups both before (p = 0.36) and after IPTW was applied (p = 0.81). Although the incidence of extrahepatic malignancy was significantly higher in the ETV group than in the TDF group before weighting (p = 0.02), no difference was confirmed after IPTW (p = 0.29). The cumulative incidence rates of death or liver transplantation, liver-related outcome, new cirrhosis development, and decompensation events were also comparable in the crude population (p = 0.24–0.91) and in the IPTW-adjusted population (p = 0.39–0.80). Both groups exhibited similar rates of CVR (ETV vs. TDF: 95.1% vs. 95.8%, p = 0.38), and negative conversion of hepatitis B e antigen (41.6% vs. 37.2%, p = 0.09) or surface antigen (2.8% vs. 1.9%, p = 0.10). Compared to the ETV group, more patients in the TDF group changed initial antivirals due to side effects, including decreased kidney function (n = 17), hypophosphatemia (n = 20), and osteoporosis (n = 18). In this large-scale multicenter study, ETV and TDF demonstrated comparable effectiveness across a broad range of outcomes in patients with treatment-naïve CHB during similar follow-up periods.
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Seo, Yeon Seok
Anam Hospital (Department of Gastroenterology and Hepatology, Anam Hospital)
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