Clinical course of hepatitis C virus-positive patients with decompensated liver cirrhosis in the era of direct-acting antiviral treatment.

Child-Pugh class decompensated cirrhosis direct-acting antiviral hepatitis C virus hepatocellular carcinoma

Journal

Hepatology research : the official journal of the Japan Society of Hepatology
ISSN: 1386-6346
Titre abrégé: Hepatol Res
Pays: Netherlands
ID NLM: 9711801

Informations de publication

Date de publication:
May 2021
Historique:
revised: 16 12 2020
received: 27 10 2020
accepted: 05 01 2021
pubmed: 29 1 2021
medline: 29 1 2021
entrez: 28 1 2021
Statut: ppublish

Résumé

The aim of the present study was to investigate the clinical course in hepatitis C virus (HCV)-positive patients with decompensated liver cirrhosis after direct-acting antivirals (DAAs) have been used for HCV infection. This multicenter study prospectively analyzed a registered cohort composed of 73 HCV-positive patients with decompensated cirrhosis who attended our 11 institutions between January 2018 and July 2018. Prognoses, including changes in the liver reserve, hepatocellular carcinoma (HCC), decompensation events, and survival, were analyzed up to July 2020, as was the initiation of DAA treatment. Sixty-four (87.7%) and nine (12.3%) patients had Child-Pugh class (C-P) B and C at baseline, respectively. Within 2 years after enrollment, 17 patients (23.3%) received treatment with DAAs, and 31 patients (42.5%) developed uncontrolled HCC, switched to palliative care, or died. Patients who received DAA treatment were significantly younger and had significantly higher alanine aminotransferase levels and lower platelet counts than the patients who did not receive DAA treatment. The rates of overall survival, cumulative HCC occurrence, and cumulative hospitalization for any hepatic decompensation event at 2 years were 64.8%, 13.1%, and 65.6%, respectively. Overall survival was significantly shorter and the HCC occurrence and hospitalization rates were significantly higher in C-P C patients than in C-P B patients. Among HCV-positive patients with decompensated cirrhosis, approximately one-fourth received DAA treatment, but more than 40% of the patients lost the opportunity for treatment with DAAs.

Identifiants

pubmed: 33507588
doi: 10.1111/hepr.13623
doi:

Types de publication

Journal Article

Langues

eng

Pagination

517-527

Subventions

Organisme : Gilead Sciences
Organisme : Japan Agency for Medical Research and Development
ID : JP20fk0210058

Informations de copyright

© 2021 The Japan Society of Hepatology.

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Auteurs

Kazuki Maesaka (K)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Ryotaro Sakamori (R)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Ryoko Yamada (R)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Yuki Tahata (Y)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Masahide Oshita (M)

Department of Gastroenterology and Hepatology, Osaka Police Hospital, Osaka, Japan.

Hideki Hagiwara (H)

Department of Gastroenterology and Hepatology, Kansai Rosai Hospital, Amagasaki, Hyogo, Japan.

Mitsuru Sakakibara (M)

Department of Gastroenterology and Hepatology, Yao Municipal Hospital, Yao, Osaka, Japan.

Shinji Tamura (S)

Department of Gastroenterology and Hepatology, Minoh City Hospital, Minoh, Osaka, Japan.

Naoki Hiramatsu (N)

Department of Gastroenterology and Hepatology, Osaka Rosai Hospital, Sakai, Osaka, Japan.

Masami Inada (M)

Department of Gastroenterology and Hepatology, Toyonaka Municipal Hospital, Toyonaka, Osaka, Japan.

Sadaharu Iio (S)

Department of Gastroenterology and Hepatology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Hyogo, Japan.

Toshifumi Ito (T)

Department of Gastroenterology and Hepatology, Japan Community Healthcare Organization, Osaka Hospital, Osaka, Japan.

Takayuki Yakushijin (T)

Department of Gastroenterology and Hepatology, Osaka General Medical Center, Osaka, Japan.

Yoshinori Doi (Y)

Department of Gastroenterology and Hepatology, Otemae Hospital, Osaka, Japan.

Takahiro Kodama (T)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Hayato Hikita (H)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Tomohide Tatsumi (T)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Tetsuo Takehara (T)

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.

Classifications MeSH