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Tenofovir Versus Entecavir for Hepatocellular Carcinoma Prevention in an International Consortium of Chronic Hepatitis B.
Hsu, Yao-Chun; Wong, Grace Lai-Hung; Chen, Chien-Hung; Peng, Cheng-Yuan; Yeh, Ming-Lun; Cheung, Ka-Shing; Toyoda, Hidenori; Huang, Chung-Feng; Trinh, Huy; Xie, Qing; Enomoto, Masaru; Liu, Li; Yasuda, Satoshi; Tanaka, Yasuhito; Kozuka, Ritsuzo; Tsai, Pei-Chien; Huang, Yen-Tsung; Wong, Christopher; Huang, Rui; Jang, Tyng-Yuan; Hoang, Joseph; Yang, Hwai-I; Li, Jiayi; Lee, Dong-Hyun; Takahashi, Hirokazu; Zhang, Jian Q; Ogawa, Eiichi; Zhao, Changqing; Liu, Chenghai; Furusyo, Norihiro; Eguchi, Yuichiro; Wong, Clifford; Wu, Chao; Kumada, Takashi; Yuen, Man-Fung; Yu, Ming-Lung; Nguyen, Mindie H.
Afiliação
  • Hsu YC; Division of Gastroenterology and Hepatology, E-Da Hospital, Kaohsiung, Taiwan.
  • Wong GL; Division of Gastroenterology, Fu-Jen Catholic University Hospital, New Taipei, Taiwan.
  • Chen CH; School of Medicine, Fu-Jen Catholic University, New Taipei, Taiwan.
  • Peng CY; Graduate Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.
  • Yeh ML; Department of Medicine and Therapeutics, the Chinese University of Hong Kong, Hong Kong SAR, China.
  • Cheung KS; Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Toyoda H; Department of Gastroenterology, China Medical University Hospital, Taichung, Taiwan.
  • Huang CF; Department of Internal Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Trinh H; Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.
  • Xie Q; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Enomoto M; San Jose Gastroenterology, San Jose, California, USA.
  • Liu L; Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
  • Yasuda S; Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Tanaka Y; Department of Infection Disease, the Third Hospital of Kumming City, Kumming, People's Republic of China.
  • Kozuka R; Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Tsai PC; Institute of Statistical Science, Academia Sinica, Taipei, Taiwan.
  • Huang YT; Wong Clinics, San Francisco, California, USA.
  • Wong C; Department of Infectious Diseases, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, Jiangsu, People's Republic of China.
  • Huang R; Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, the United States of America.
  • Jang TY; Genomics Research Center, Academia Sinica, Taipei, Taiwan.
  • Hoang J; Palo Alto Medical Foundation, Mountain View Division, Mountain View, California, USA.
  • Yang HI; Department of Gastroenterology, Good Gang-An Hospital, Busan, Sourth Korea.
  • Li J; Department of Internal Medicine, Saga University Hospital, Saga, Japan.
  • Lee DH; Chinese Hospital, San Francisco, California, USA.
  • Takahashi H; Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Zhang JQ; Department of Cirrhosis, Institute of Liver Disease, Shuguang Hospital affiliated to Shanghai University of T.C.M., Shanghai, People's Republic of China.
  • Ogawa E; Department of Medicine and Therapeutics, the Chinese University of Hong Kong, Hong Kong SAR, China.
  • Zhao C; Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Liu C; Department of Gastroenterology, China Medical University Hospital, Taichung, Taiwan.
  • Furusyo N; Department of Internal Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Eguchi Y; Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.
  • Wong C; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Wu C; Department of Internal Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Kumada T; San Jose Gastroenterology, San Jose, California, USA.
  • Yuen MF; Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
  • Yu ML; Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Nguyen MH; Department of Infection Disease, the Third Hospital of Kumming City, Kumming, People's Republic of China.
Am J Gastroenterol ; 115(2): 271-280, 2020 02.
Article em En | MEDLINE | ID: mdl-31634265
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Carcinoma Hepatocelular / Hepatite B Crônica / Tenofovir / Guanina / Neoplasias Hepáticas Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Carcinoma Hepatocelular / Hepatite B Crônica / Tenofovir / Guanina / Neoplasias Hepáticas Idioma: En Ano de publicação: 2020 Tipo de documento: Article