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- Publisher Website: 10.14309/ajg.0000000000000428
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- PMID: 31634265
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Article: Tenofovir Versus Entecavir for Hepatocellular Carcinoma Prevention in an International Consortium of Chronic Hepatitis B
Title | Tenofovir Versus Entecavir for Hepatocellular Carcinoma Prevention in an International Consortium of Chronic Hepatitis B |
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Authors | |
Issue Date | 2020 |
Publisher | Lippincott, Williams & Wilkins. The Journal's web site is located at https://journals.lww.com/ajg/pages/default.aspx |
Citation | The American Journal of Gastroenterology, 2020, v. 115 n. 2, p. 271-280 How to Cite? |
Abstract | INTRODUCTION:
It is unclear whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) differ in their effectiveness for preventing hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB).
METHODS:
This retrospective cohort study analyzed an international consortium that encompassed 19 centers from 6 countries or regions composed of previously untreated CHB patients then treated with either ETV or TDF monotherapy. Those who developed HCC before antiviral treatment or within 1 year of therapy were excluded. The association between antiviral regimen and HCC risk was evaluated using competing-risk survival regression. We also applied propensity score matching (PSM) to 1:1 balance the 2 treatment cohorts. A total of 5,537 patients were eligible (n = 4,837 received ETV and n = 700 received TDF) and observed for HCC occurrence until December 23, 2018. Before PSM, the TDF cohort was significantly younger and had generally less advanced diseases.
RESULTS:
In the unadjusted analysis, TDF was associated with a lower risk of HCC (subdistribution hazard ratio [SHR], 0.45; 95% confidence interval [CI], 0.26–0.79; P = 0.005). The multivariable analysis, however, found that the association between TDF and HCC no longer existed (SHR, 0.81; 95% CI, 0.42–1.56; P = 0.52) after adjustment for age, sex, country, albumin, platelet, α-fetoprotein, cirrhosis, and diabetes mellitus. Furthermore, the PSM analysis (n = 1,040) found no between-cohort differences in HCC incidences (P = 0.51) and no association between regimens (TDF or ETV) and HCC risk in the multivariable-adjusted analysis (adjusted SHR, 0.89; 95% CI, 0.41–1.92; P = 0.77).
DISCUSSION:
TDF and ETV did not significantly differ in the prevention of HCC in patients with CHB. |
Persistent Identifier | http://hdl.handle.net/10722/284489 |
ISSN | 2023 Impact Factor: 8.0 2023 SCImago Journal Rankings: 2.391 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Hsu, YC | - |
dc.contributor.author | Wong, GLH | - |
dc.contributor.author | Chen, CH | - |
dc.contributor.author | Peng, CY | - |
dc.contributor.author | Yeh, ML | - |
dc.contributor.author | Cheung, KS | - |
dc.contributor.author | Toyoda, H | - |
dc.contributor.author | Huang, CF | - |
dc.contributor.author | Trinh, H | - |
dc.contributor.author | Xie, Q | - |
dc.contributor.author | Enomoto, M | - |
dc.contributor.author | Liu, L | - |
dc.contributor.author | Yasuda, S | - |
dc.contributor.author | Tanaka, Y | - |
dc.contributor.author | Kozuka, R | - |
dc.contributor.author | Tsai, PC | - |
dc.contributor.author | Huang, YT | - |
dc.contributor.author | Wong, C | - |
dc.contributor.author | Huang, R | - |
dc.contributor.author | Jang, TY | - |
dc.contributor.author | Hoang, J | - |
dc.contributor.author | Yan, HI | - |
dc.contributor.author | Li, J | - |
dc.contributor.author | Lee, DH | - |
dc.contributor.author | Takahashi, H | - |
dc.contributor.author | Zhang, JQ | - |
dc.contributor.author | Ogawa, E | - |
dc.contributor.author | Zhao, C | - |
dc.contributor.author | Liu, C | - |
dc.contributor.author | Furusyo, N | - |
dc.contributor.author | Eguchi, Y | - |
dc.contributor.author | Wong, C | - |
dc.contributor.author | Wu, C | - |
dc.contributor.author | Kumada, T | - |
dc.contributor.author | Yuen, MF | - |
dc.contributor.author | Yu, ML | - |
dc.contributor.author | Nguyen, M | - |
dc.date.accessioned | 2020-08-07T08:58:23Z | - |
dc.date.available | 2020-08-07T08:58:23Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | The American Journal of Gastroenterology, 2020, v. 115 n. 2, p. 271-280 | - |
dc.identifier.issn | 0002-9270 | - |
dc.identifier.uri | http://hdl.handle.net/10722/284489 | - |
dc.description.abstract | INTRODUCTION: It is unclear whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) differ in their effectiveness for preventing hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). METHODS: This retrospective cohort study analyzed an international consortium that encompassed 19 centers from 6 countries or regions composed of previously untreated CHB patients then treated with either ETV or TDF monotherapy. Those who developed HCC before antiviral treatment or within 1 year of therapy were excluded. The association between antiviral regimen and HCC risk was evaluated using competing-risk survival regression. We also applied propensity score matching (PSM) to 1:1 balance the 2 treatment cohorts. A total of 5,537 patients were eligible (n = 4,837 received ETV and n = 700 received TDF) and observed for HCC occurrence until December 23, 2018. Before PSM, the TDF cohort was significantly younger and had generally less advanced diseases. RESULTS: In the unadjusted analysis, TDF was associated with a lower risk of HCC (subdistribution hazard ratio [SHR], 0.45; 95% confidence interval [CI], 0.26–0.79; P = 0.005). The multivariable analysis, however, found that the association between TDF and HCC no longer existed (SHR, 0.81; 95% CI, 0.42–1.56; P = 0.52) after adjustment for age, sex, country, albumin, platelet, α-fetoprotein, cirrhosis, and diabetes mellitus. Furthermore, the PSM analysis (n = 1,040) found no between-cohort differences in HCC incidences (P = 0.51) and no association between regimens (TDF or ETV) and HCC risk in the multivariable-adjusted analysis (adjusted SHR, 0.89; 95% CI, 0.41–1.92; P = 0.77). DISCUSSION: TDF and ETV did not significantly differ in the prevention of HCC in patients with CHB. | - |
dc.language | eng | - |
dc.publisher | Lippincott, Williams & Wilkins. The Journal's web site is located at https://journals.lww.com/ajg/pages/default.aspx | - |
dc.relation.ispartof | The American Journal of Gastroenterology | - |
dc.rights | This is a non-final version of an article published in final form in (provide complete journal citation) | - |
dc.title | Tenofovir Versus Entecavir for Hepatocellular Carcinoma Prevention in an International Consortium of Chronic Hepatitis B | - |
dc.type | Article | - |
dc.identifier.email | Cheung, KS: cks634@hku.hk | - |
dc.identifier.email | Yuen, MF: mfyuen@hku.hk | - |
dc.identifier.authority | Cheung, KS=rp02532 | - |
dc.identifier.authority | Yuen, MF=rp00479 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.14309/ajg.0000000000000428 | - |
dc.identifier.pmid | 31634265 | - |
dc.identifier.scopus | eid_2-s2.0-85079018521 | - |
dc.identifier.hkuros | 312205 | - |
dc.identifier.volume | 115 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 271 | - |
dc.identifier.epage | 280 | - |
dc.identifier.isi | WOS:000540835600021 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0002-9270 | - |