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Hepatitis C Virus Cure Rates Are Reduced in Patients With Active but Not Inactive Hepatocellular Carcinoma: A Practice Implication.
Ogawa, Eiichi; Toyoda, Hidenori; Iio, Etsuko; Jun, Dae Won; Huang, Chung-Feng; Enomoto, Masaru; Hsu, Yao-Chun; Haga, Hiroaki; Iwane, Shinji; Wong, Grace; Lee, Dong Hyun; Tada, Toshifumi; Liu, Chen-Hua; Chuang, Wan-Long; Hayashi, Jun; Cheung, Ramsey; Yasuda, Satoshi; Tseng, Cheng-Hao; Takahashi, Hirokazu; Tran, Sally; Yeo, Yee Hui; Henry, Linda; Barnett, Scott D; Nomura, Hideyuki; Nakamuta, Makoto; Dai, Chia-Yen; Huang, Jee-Fu; Yang, Hwai-I; Lee, Mei-Hsuan; Jun, Mi Jung; Kao, Jia-Horng; Eguchi, Yuichiro; Ueno, Yoshiyuki; Tamori, Akihiro; Furusyo, Norihiro; Yu, Ming-Lung; Tanaka, Yasuhito; Nguyen, Mindie H.
Affiliation
  • Ogawa E; Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Toyoda H; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Iio E; Department of Virology and Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Jun DW; Department of Gastroenterology, Hanyang University, Seoul, South Korea.
  • Huang CF; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Enomoto M; Department of Hepatology, Osaka City University Graduate School of Medicine, Osaka, Japan.
  • Hsu YC; Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Hospital, Kaohsiung, Taiwan.
  • Haga H; Department of Gastroenterology, Yamagata University Faculty of Medicine, Yamagata, Japan.
  • Iwane S; Liver Center, Saga University Hospital, Saga, Japan.
  • Wong G; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong.
  • Lee DH; State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong.
  • Tada T; Department of Gastroenterology, Good Gang-An Hospital, Busan, Korea.
  • Liu CH; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Chuang WL; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Hayashi J; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
  • Cheung R; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Yasuda S; Kyushu General Internal Medicine Center, Haradoi Hospital, Fukuoka, Japan.
  • Tseng CH; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
  • Takahashi H; Division of Gastroenterology and Hepatology, Veterans Affairs Palo Alto Health Care System, Palo Alto, California, USA.
  • Tran S; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Yeo YH; Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Hospital, Kaohsiung, Taiwan.
  • Henry L; Liver Center, Saga University Hospital, Saga, Japan.
  • Barnett SD; Division of Metabolism and Endocrinology, Saga University Faculty of Medicine, Saga, Japan.
  • Nomura H; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
  • Nakamuta M; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
  • Dai CY; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
  • Huang JF; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, California, USA.
  • Yang HI; The Center for Liver Disease, Shin-Kokura Hospital, Kitakyushu, Japan.
  • Lee MH; Department of Gastroenterology, Kyushu Medical Center, National Hospital Organization, Fukuoka, Japan.
  • Jun MJ; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Kao JH; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
  • Eguchi Y; Genomics Research Center, Academia Sinica, Taipei, Taiwan.
  • Ueno Y; Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan.
  • Tamori A; Department of Gastroenterology, Good Gang-An Hospital, Busan, Korea.
  • Furusyo N; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Yu ML; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan.
  • Tanaka Y; Liver Center, Saga University Hospital, Saga, Japan.
  • Nguyen MH; Department of Gastroenterology, Yamagata University Faculty of Medicine, Yamagata, Japan.
Clin Infect Dis ; 71(11): 2840-2848, 2020 12 31.
Article in En | MEDLINE | ID: mdl-31777940
BACKGROUND: Cure rates of hepatitis C virus (HCV) treatment with direct-acting antivirals (DAAs) for patients with active and inactive hepatocellular carcinoma (HCC) may differ, but well-controlled studies are limited. We aimed to evaluate DAA outcomes in a large East Asian HCV/HCC population compared with HCV/non-HCC patients. METHODS: Using data from the Real-World Evidence from the Asia Liver Consortium (REAL-C) registry (Hong Kong, Japan, South Korea, and Taiwan), we used propensity score matching (PSM) to match HCC and non-HCC (1:1) groups for age, sex, cirrhosis, prior treatment, HCV genotype, treatment regimen, baseline platelet count, HCV RNA, total bilirubin, alanine aminotransferase, and albumin levels to evaluate DAA treatment outcomes in a large population of HCV/HCC compared with HCV/non-HCC patients. RESULTS: We included 6081 patients (HCC, n = 465; non-HCC, n = 5 616) treated with interferon-free DAAs. PSM of the entire study population yielded 436 matched pairs with similar baseline characteristics. There was no statistically significant difference in the overall SVR rate of HCC (92.7%) and non-HCC (95.0%) groups. Rates of treatment discontinuation, adverse effects, and death were also similar between HCC and non-HCC groups. Among patients with HCC, those with active HCC had a lower SVR than inactive HCC cases (85.5% vs 93.7%; P = .03). On multivariable analysis, active HCC, but not inactive HCC, was significantly associated with lower SVR (OR, 0.28; P = .01) when compared with non-HCC. CONCLUSIONS: Active HCC but not inactive HCC was independently associated with lower SVR compared with non-HCC patients undergoing DAA therapy, although cure rate was still relatively high (85%) in active HCC patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Carcinoma, Hepatocellular / Hepatitis C, Chronic / Liver Neoplasms Limits: Humans Country/Region as subject: Asia Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2020 Document type: Article Affiliation country: Japan Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatitis C / Carcinoma, Hepatocellular / Hepatitis C, Chronic / Liver Neoplasms Limits: Humans Country/Region as subject: Asia Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2020 Document type: Article Affiliation country: Japan Country of publication: United States