Efficacy of hepatitis C virus eradication after curative treatment for hepatocellular carcinoma in patients with advanced hepatocellular carcinoma and decreased hepatic functional reserve: A nationwide, multicentre study by the Japanese Red Cross Liver Study Group.


Journal

Journal of viral hepatitis
ISSN: 1365-2893
Titre abrégé: J Viral Hepat
Pays: England
ID NLM: 9435672

Informations de publication

Date de publication:
07 2022
Historique:
received: 03 03 2022
accepted: 11 04 2022
pubmed: 14 5 2022
medline: 11 6 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

Improvements in the hepatocellular carcinoma (HCC) recurrence rate and survival have been frequently reported following virus eradication after hepatitis C virus (HCV)-related HCC cure. However, the efficacy of direct-acting antiviral (DAA) therapy in patients who included those with advanced HCC and decreased hepatic functional reserve is unknown. A comparative examination was retrospectively conducted of 141 patients with hepatitis C who started DAA therapy within 1 year after undergoing curative HCC treatment and showed a sustained viral response (SVR) and 327 patients who underwent curative treatment for HCV-related HCC and did not subsequently receive antiviral therapy. Whether DAA therapy was given was identified as an independent factor related to both HCC recurrence and survival. Both the recurrence and survival rates improved significantly with DAA therapy in Child-Pugh (CP)-A, whereas no difference in the recurrence rate was seen with DAA therapy in CP-B. However, the survival rate was significantly higher in the DAA group in this class. Similarly, dividing the patients by the Milan criteria showed significant improvements in the recurrence rate and survival with DAA therapy in patients within the Milan criteria. Patients with HCC beyond the Milan criteria showed no difference in recurrence rates, but the DAA group tended to have higher survival rates. Thus, DAA after curative therapy for HCC can be expected to improve survival in patients with advanced HCC or decreased hepatic functional reserve. HCV should be aggressively eradicated in all patients eligible for curative treatment of HCC.

Identifiants

pubmed: 35548866
doi: 10.1111/jvh.13684
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

551-558

Informations de copyright

© 2022 John Wiley & Sons Ltd.

Références

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Auteurs

Toshie Mashiba (T)

Center for Liver-Biliary-Pancreatic Disease, Matsuyama Red Cross Hospital, Ehime, Japan.

Kouji Joko (K)

Center for Liver-Biliary-Pancreatic Disease, Matsuyama Red Cross Hospital, Ehime, Japan.

Masayuki Kurosaki (M)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

Hironori Ochi (H)

Center for Liver-Biliary-Pancreatic Disease, Matsuyama Red Cross Hospital, Ehime, Japan.

Hiroyuki Marusawa (H)

Department of Gastroenterology and Hepatology, Osaka Red Cross Hospital, Osaka, Japan.

Yasushi Uchida (Y)

Department of Gastroenterology, Matsue Red Cross Hospital, Shimane, Japan.

Hideki Fujii (H)

Department of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.

Yuji Kojima (Y)

Department of Hepatology, Japanese Red Cross Ise Hospital, Mie, Japan.

Hideo Yoshida (H)

Department of Gastroenterology, Japanese Red Cross Medical Center, Tokyo, Japan.

Tohru Goto (T)

Department of Gastroenterology, Omori Red Cross Hospital, Tokyo, Japan.

Takehiro Akahane (T)

Department of Gastroenterology, Ishinomaki Red Cross Hospital, Miyagi, Japan.

Masahiko Kondo (M)

Department of Gastroenterology, Otsu Red Cross Hospital, Shiga, Japan.

Keiji Tsuji (K)

Department of Gastroenterology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Hiroshima, Japan.

Akeri Mitsuda (A)

Department of Internal Medicine, Japanese Red Cross Tottori Hospital, Tottori, Japan.

Chitomi Hasebe (C)

Department of Gastroenterology, Japanese Red Cross Asahikawa Hospital, Hokkaido, Japan.

Atsunori Kusakabe (A)

Department of Gastroenterology, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Aichi, Japan.

Tetsuro Sohda (T)

Hepatology Division, Japanese Red Cross Fukuoka Hospital, Fukuoka, Japan.

Koichiro Furuta (K)

Department of Gastroenterology, Masuda Red Cross Hospital, Shimane, Japan.

Haruhiko Kobashi (H)

Department of Gastroenterology, Japanese Red Cross Okayama Hospital, Okayama, Japan.

Chikara Ogawa (C)

Department of Gastroenterology, Takamatsu Red Cross Hospital, Kagawa, Japan.

Yasushi Ide (Y)

Department of Internal Medicine, Karatsu Red Cross Hospital, Saga, Japan.

Hirotaka Arai (H)

Department of Gastroenterology, Maebashi Red Cross Hospital, Gunma, Japan.

Kazuhiko Okada (K)

Department of Gastroenterology, Toyama Red Cross Hospital, Toyama, Japan.

Masaya Shigeno (M)

Department of Gastroenterology, Japanese Red Cross Nagasaki Genbaku Hospital, Nagasaki, Japan.

Riko Nonogi (R)

Department of Gastroenterology, Tokushima Red Cross Hospital, Tokushima, Japan.

Namiki Izumi (N)

Department of Gastroenterology and Hepatology, Musashino Red Cross Hospital, Tokyo, Japan.

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