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HCC risk post-SVR with DAAs in East Asians: findings from the REAL-C cohort.
Tanaka, Yasuhito; Ogawa, Eiichi; Huang, Chung-Feng; Toyoda, Hidenori; Jun, Dae Won; Tseng, Cheng-Hao; Hsu, Yao-Chun; Enomoto, Masaru; Takahashi, Hirokazu; Furusyo, Norihiro; Yeh, Ming-Lun; Iio, Etsuko; Yasuda, Satoshi; Lam, Carla Pui-Mei; Lee, Dong Hyun; Haga, Hiroaki; Yoon, Eileen L; Ahn, Sang Bong; Wong, Grace; Nakamuta, Makoto; Nomura, Hideyuki; Tsai, Pei-Chien; Jung, Jang Han; Song, Do Seon; Dang, Hansen; Maeda, Mayumi; Henry, Linda; Cheung, Ramsey; Yuen, Man-Fung; Ueno, Yoshiyuki; Eguchi, Yuichiro; Tamori, Akihiro; Yu, Ming-Lung; Hayashi, Jun; Nguyen, Mindie H.
Affiliation
  • Tanaka Y; Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Ogawa E; Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Huang CF; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Toyoda H; Hepatitis Research Center, College of Medicine and Cohort Research Center, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Jun DW; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Tseng CH; Department of Gastroenterology, Hanyang University, Seoul, South Korea.
  • Hsu YC; Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Cancer Hospital, Kaohsiung, Taiwan.
  • Enomoto M; Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Cancer Hospital, Kaohsiung, Taiwan.
  • Takahashi H; Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Furusyo N; Liver Center, Saga University Hospital, Saga, Japan.
  • Yeh ML; Division of Metabolism and Endocrinology, Saga University Faculty of Medicine, Saga, Japan.
  • Iio E; Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Yasuda S; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Lam CP; Hepatitis Research Center, College of Medicine and Cohort Research Center, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Lee DH; Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Haga H; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Yoon EL; Department of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.
  • Ahn SB; Department of Gastroenterology, Good Gang-An Hospital, Busan, Korea.
  • Wong G; Department of Gastroenterology, Yamagata University Faculty of Medicine, Yamagata, Japan.
  • Nakamuta M; Department of Internal Medicine, Inje University Sanggye Paik Hospital, Seoul, South Korea.
  • Nomura H; Department of Internal Medicine, Nowon Eulji Medical Center, Eulji University College of Medicine, Seoul, South Korea.
  • Tsai PC; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
  • Jung JH; State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
  • Song DS; Department of Gastroenterology, Kyushu Medical Center, National Hospital Organization, Fukuoka, Japan.
  • Dang H; Department of Internal Medicine, Haradoi Hospital, Fukuoka, Japan.
  • Maeda M; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
  • Henry L; Hepatitis Research Center, College of Medicine and Cohort Research Center, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Cheung R; Department of Internal Medicine, Hallym University Dongtan Sacred Heart Hospital, Hwaseong, South Korea.
  • Yuen MF; Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
  • Ueno Y; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, 780 Welch Road, Palo Alto, CA, 94304, USA.
  • Eguchi Y; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, 780 Welch Road, Palo Alto, CA, 94304, USA.
  • Tamori A; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, 780 Welch Road, Palo Alto, CA, 94304, USA.
  • Yu ML; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, 780 Welch Road, Palo Alto, CA, 94304, USA.
  • Hayashi J; Division of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, USA.
  • Nguyen MH; Department of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong.
Hepatol Int ; 14(6): 1023-1033, 2020 Dec.
Article in En | MEDLINE | ID: mdl-33277685
ABSTRACT

BACKGROUND:

Despite HCV cure, patients remain at risk for HCC, but risk factor data for HCC following SVR are limited for Asian patients.

METHODS:

To address this gap, we analyzed 5814 patients (5646 SVR, 168 non-SVR) from the Real-World Evidence from the Asia Liver Consortium for HCV (REAL-C) who did not have HCC or a history of HCC at baseline (pre-DAA treatment) and did not develop HCC within 6 months of baseline. To assess the effect of SVR on HCC incidence, we used 14 propensity score matching [(PSM), age, sex, baseline cirrhosis, and baseline AFP] to balance the SVR and non-SVR groups.

RESULTS:

In the PSM cohort (160 non-SVR and 612 SVR), the HCC incidence rate per 100 person years was higher in the non-SVR compared to the SVR group (5.26 vs. 1.94, p < 0.001). Achieving SVR was independently associated with decreased HCC risk (adjusted HR [aHR] 0.41, p = 0.002). Next, we stratified the SVR cohort of 5646 patients to cirrhotic and noncirrhotic subgroups. Among cirrhotic SVR patients, aged ≥ 60, having an albumin bilirubin grade (ALBI) of 2 or 3 (aHR 2.5, p < 0.001), and baseline AFP ≥ 10 ng/mL (aHR 1.6, p = 0.001) were associated with higher HCC risk, while among the non-cirrhotic SVR group, only baseline AFP ≥ 10 ng/mL was significant (aHR 4.26, p = 0.005).

CONCLUSIONS:

Achieving SVR decreases HCC risk; however, among East Asians, patients with elevated pretreatment AFP remained at risk. Pretreatment AFP, an easily obtained serum marker, may provide both prognostic and surveillance value for HCC in East Asian patients who obtained SVR.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Hepatocellular / Liver Neoplasms Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Middle aged Language: En Journal: Hepatol Int Year: 2020 Document type: Article Affiliation country: Japan Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Hepatocellular / Liver Neoplasms Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Middle aged Language: En Journal: Hepatol Int Year: 2020 Document type: Article Affiliation country: Japan Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA