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Antiviral therapy substantially reduces HCC risk in patients with chronic hepatitis B infection in the indeterminate phase.
Huang, Daniel Q; Tran, Andrew; Yeh, Ming-Lun; Yasuda, Satoshi; Tsai, Pei-Chien; Huang, Chung-Feng; Dai, Chia Yen; Ogawa, Eiichi; Ishigami, Masatoshi; Ito, Takanori; Kozuka, Ritsuzo; Enomoto, Masaru; Suzuki, Takanori; Yoshimaru, Yoko; Preda, Carmen M; Marin, Raluca I; Sandra, Irina; Tran, Sally; Quek, Sabrina X Z; Khine, Htet Htet Toe Wai; Itokawa, Norio; Atsukawa, Masanori; Uojima, Haruki; Watanabe, Tsunamasa; Takahashi, Hirokazu; Inoue, Kaori; Maeda, Mayumi; Hoang, Joseph K; Trinh, Lindsey; Barnett, Scott; Cheung, Ramsey; Lim, Seng Gee; Trinh, Huy N; Chuang, Wan-Long; Tanaka, Yasuhito; Toyoda, Hidenori; Yu, Ming-Lung; Nguyen, Mindie H.
Afiliação
  • Huang DQ; Department of Medicine, Division of Gastroenterology and Hepatology, National University Hospital, Singapore, Singapore.
  • Tran A; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Yeh ML; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Yasuda S; Department of Internal Medicine, Hepatobiliary Division, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Tsai PC; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Huang CF; Department of Internal Medicine, Hepatobiliary Division, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Dai CY; Department of Internal Medicine, Hepatobiliary Division, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Ogawa E; Department of Internal Medicine, Hepatobiliary Division, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Ishigami M; Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Ito T; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Kozuka R; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Enomoto M; Department of Hepatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
  • Suzuki T; Department of Hepatology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
  • Yoshimaru Y; Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Science, Nagoya, Japan.
  • Preda CM; Department of Gastroenterology and Hepatology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
  • Marin RI; Department of Gastroenterology and Hepatology, Clinic Fundeni Institute, Bucharest, Romania.
  • Sandra I; Department of Gastroenterology and Hepatology, Clinic Fundeni Institute, Bucharest, Romania.
  • Tran S; Department of Gastroenterology and Hepatology, Clinic Fundeni Institute, Bucharest, Romania.
  • Quek SXZ; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Khine HHTW; Department of Medicine, Division of Gastroenterology and Hepatology, National University Hospital, Singapore, Singapore.
  • Itokawa N; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Atsukawa M; Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Uojima H; Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Watanabe T; Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
  • Takahashi H; Division of Gastroenterology and Hepatology, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Inoue K; Liver Center, Saga University Hospital, Saga, Japan.
  • Maeda M; Liver Center, Saga University Hospital, Saga, Japan.
  • Hoang JK; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Trinh L; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Barnett S; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Cheung R; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Lim SG; Department of Medicine, Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.
  • Trinh HN; Department of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Healthcare, Palo Alto, California, USA.
  • Chuang WL; Department of Medicine, Division of Gastroenterology and Hepatology, National University Hospital, Singapore, Singapore.
  • Tanaka Y; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Toyoda H; San Jose Gastroenterology, San Jose, California, USA.
  • Yu ML; Department of Internal Medicine, Hepatobiliary Division, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Nguyen MH; Department of Gastroenterology and Hepatology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.
Hepatology ; 78(5): 1558-1568, 2023 11 01.
Article em En | MEDLINE | ID: mdl-37184202
ABSTRACT
BACKGROUND AND

AIMS:

HCC risk in chronic hepatitis B (CHB) is higher in the indeterminate phase compared with the inactive phase. However, it is unclear if antiviral therapy reduces HCC risk in this population. We aimed to evaluate the association between antiviral therapy and HCC risk in the indeterminate phase. APPROACH AND

RESULTS:

We analyzed 855 adult (59% male), treatment-naïve patients with CHB infection without advanced fibrosis in the indeterminate phase at 14 centers (USA, Europe, and Asia). Inverse probability of treatment weighting (IPTW) was used to balance the treated (n = 405) and untreated (n = 450) groups. The primary outcome was HCC development. The mean age was 46±13 years, the median alanine transaminase was 38 (interquartile range, 24-52) U/L, the mean HBV DNA was 4.5±2.1 log 10 IU/mL, and 20% were HBeAg positive. The 2 groups were similar after IPTW. After IPTW (n = 819), the 5-, 10-, and 15-year cumulative HCC incidence was 3%, 4%, and 9% among treated patients (n = 394) versus 3%, 15%, and 19%, among untreated patients (n = 425), respectively ( p = 0.02), with consistent findings in subgroup analyses for age >35 years, males, HBeAg positive, HBV DNA>1000 IU/mL, and alanine transaminasehazards analysis adjusted for age, sex, HBeAg, HBV DNA, alanine transaminase, diabetes, and platelets, antiviral therapy remained an independent predictor of reduced HCC risk (adjusted HR = 0.3, 95% CI 0.1-0.6, p = 0.001).

CONCLUSIONS:

Antiviral therapy reduces HCC risk by 70% among patients with indeterminate-phase CHB. These data have important implications for the potential expansion of CHB treatment criteria.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Hepatite B Crônica / Hepatite B / Neoplasias Hepáticas Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatology Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Hepatite B Crônica / Hepatite B / Neoplasias Hepáticas Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatology Ano de publicação: 2023 Tipo de documento: Article