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Non-liver-related mortality in the DAA era: Insights from post-SVR patients with and without previous HCC history.
Miuma, Satoshi; Miyaaki, Hisamitsu; Ichikawa, Tatsuki; Matsuzaki, Toshihisa; Goto, Takashi; Kamo, Yasuhiro; Shigeno, Masaya; Hino, Naoyuki; Ario, Keisuke; Yanagi, Kenji; Tsutsumi, Takuya; Fukushima, Nobuyoshi; Nakashiki, Suguru; Yamasaki, Kazufumi; Hamasaki, Keisuke; Shibata, Hidetaka; Arima, Kazuhiko; Yamamichi, Shinobu; Yamashima, Mio; Takahashi, Kosuke; Nakao, Yasuhiko; Fukushima, Masanori; Haraguchi, Masafumi; Sasaki, Ryu; Ozawa, Eisuke; Taura, Naota; Nakao, Kazuhiko.
Afiliação
  • Miuma S; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Miyaaki H; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Ichikawa T; Department of Gastroenterology, Nagasaki Harbor Medical Center City Hospital, Nagasaki, Japan.
  • Matsuzaki T; Department of Gastroenterology, Sasebo City General Medical Center, Sasebo, Japan.
  • Goto T; Department of Gastroenterology, Nagasaki Rosai Hospital, Sasebo, Japan.
  • Kamo Y; Department of Gastroenterology, Hakujujikai Sasebo Chuo Hospital, Sasebo, Japan.
  • Shigeno M; Department of Gastroenterology, Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki, Japan.
  • Hino N; Department of Gastroenterology, National Hospital Organization Ureshino Medical Center, Ureshino, Japan.
  • Ario K; Department of Gastroenterology, National Hospital Organization Ureshino Medical Center, Ureshino, Japan.
  • Yanagi K; Department of Gastroenterology, Nijigaoka Hospital, Nagasaki, Japan.
  • Tsutsumi T; Department of Gastroenterology, Nijigaoka Hospital, Nagasaki, Japan.
  • Fukushima N; Department of Gastroenterology, Nagasaki Goto Chuo Hospital, Goto, Japan.
  • Nakashiki S; Department of Gastroenterology, Inoue Hospital, Nagasaki, Japan.
  • Yamasaki K; Department of Gastroenterology, Saint Francis Hospital, Nagasaki, Japan.
  • Hamasaki K; Department of Gastroenterology, Caritas Clinic, Nagasaki, Japan.
  • Shibata H; Gastroenterology and Hepatology, Shibata Chokodo Hospital, Shimabara, Japan.
  • Arima K; Department of Public Health, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Yamamichi S; Department of Gastroenterology, Nagasaki Harbor Medical Center City Hospital, Nagasaki, Japan.
  • Yamashima M; Department of Gastroenterology, Nagasaki Harbor Medical Center City Hospital, Nagasaki, Japan.
  • Takahashi K; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Nakao Y; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Fukushima M; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Haraguchi M; Department of Gastroenterology, Koebaru Chuo Hospital, Nagasaki, Japan.
  • Sasaki R; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Ozawa E; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Taura N; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Nakao K; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
J Med Virol ; 96(3): e29432, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38509793
ABSTRACT
BACKGROUND AND

AIMS:

Mortality after sustained virological response (SVR) with interferon-free direct-acting antiviral (IFN-free DAA) therapy is crucial for optimizing post-SVR patient care, but it remains unclear, especially regarding non-liver-related mortality.

METHODS:

Consecutive post-SVR patients from 14 institutions were stratified into three cohorts A (without advanced fibrosis and without prior HCC), B (with advanced fibrosis and without prior HCC), and C (curative HCC treatment). We assessed mortality (per 1000 person-years [/1000PY]) post-SVR. Mortality rates were compared between cohorts A and B and the general population using age- and sex-adjusted standardized mortality ratio (SMR). Comparison of survival between each cohort was performed using propensity-score (PS) matching with sex, age, and comorbidity.

RESULTS:

In cohort A (n = 762; median age, 65 years), 22 patients died (median follow-up, 36 months); all-cause mortality was 10.0/1000PY, with 86.4% non-liver-related deaths. In cohort B (n = 519; median age, 73 years), 27 patients died (median follow-up, 39 months); all-cause mortality was 16.7/1000PY, with 88.9% non-liver-related deaths. In both cohorts, malignant neoplasm was the most common cause of death; all-cause mortality was comparable to that of the general population (SMR 0.96 and 0.92). In cohort C (n = 108; median age, 75 years), 15 patients died (median follow-up, 51 months); all-cause mortality was 36.0/1000PY, with 53.3% liver-related deaths. PS matching showed no significant survival differences between cohorts A and B, both of which had better survival than cohort C.

CONCLUSIONS:

Mortality varies based on HCC history in the DAA era; nevertheless, attention should be paid to non-liver-related deaths in all post-SVR patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Hepatite C Crônica / Neoplasias Hepáticas Limite: Aged / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma Hepatocelular / Hepatite C Crônica / Neoplasias Hepáticas Limite: Aged / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article