Comparison of postoperative outcomes in cases achieving sustained virological response with direct-acting antiviral and interferon therapy.

direct-acting antiviral hepatitis C hepatitis C virus treatment hepatocellular carcinoma sustained virological response

Journal

Journal of hepato-biliary-pancreatic sciences
ISSN: 1868-6982
Titre abrégé: J Hepatobiliary Pancreat Sci
Pays: Japan
ID NLM: 101528587

Informations de publication

Date de publication:
22 Dec 2023
Historique:
revised: 23 10 2023
received: 25 07 2023
accepted: 15 11 2023
medline: 23 12 2023
pubmed: 23 12 2023
entrez: 23 12 2023
Statut: aheadofprint

Résumé

The effect of direct-acting antiviral agents (DAAs) on hepatocellular carcinoma (HCC) recurrence after curative hepatectomy remains uncertain. This retrospective study aimed to evaluate the effect of sustained virological response (SVR) with DAAs or interferon (IFN) therapy on recurrence and overall survival (OS) after hepatectomy. We enrolled 593 patients who underwent curative resections between January 2010 and December 2017. Among them, 186 achieved SVR before hepatectomy: a total of 51 (27.4%) in the DAA-SVR group and 132 (72.6%) in the IFN-based SVR group. SVR before hepatectomy was an independent predictor of OS, and the 5-year OS rate was significantly higher in the SVR group than that in the non-SVR group (82.2% vs. 63.9%). There were no significant differences in the recurrence rates or OS between DAA and IFN treatments in achieving SVR before hepatectomy, regardless of poor hepatic function in the DAA therapy group. There was no significant difference in OS and recurrence-free survival (RFS) between the preoperative SVR achieved with DAA and IFN groups in this study, although liver function was significantly worse at the time of surgery in the DAA group compared to the IFN group.

Sections du résumé

BACKGROUND/PURPOSE OBJECTIVE
The effect of direct-acting antiviral agents (DAAs) on hepatocellular carcinoma (HCC) recurrence after curative hepatectomy remains uncertain. This retrospective study aimed to evaluate the effect of sustained virological response (SVR) with DAAs or interferon (IFN) therapy on recurrence and overall survival (OS) after hepatectomy.
METHODS METHODS
We enrolled 593 patients who underwent curative resections between January 2010 and December 2017. Among them, 186 achieved SVR before hepatectomy: a total of 51 (27.4%) in the DAA-SVR group and 132 (72.6%) in the IFN-based SVR group.
RESULTS RESULTS
SVR before hepatectomy was an independent predictor of OS, and the 5-year OS rate was significantly higher in the SVR group than that in the non-SVR group (82.2% vs. 63.9%). There were no significant differences in the recurrence rates or OS between DAA and IFN treatments in achieving SVR before hepatectomy, regardless of poor hepatic function in the DAA therapy group.
CONCLUSIONS CONCLUSIONS
There was no significant difference in OS and recurrence-free survival (RFS) between the preoperative SVR achieved with DAA and IFN groups in this study, although liver function was significantly worse at the time of surgery in the DAA group compared to the IFN group.

Identifiants

pubmed: 38135908
doi: 10.1002/jhbp.1406
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Agency for Medical Research and Development
ID : JP22fk0210065
Organisme : Japan Agency for Medical Research and Development
ID : JP23fk0210122
Organisme : Japan Society for the Promotion of Science
ID : JP22K15541

Informations de copyright

© 2023 Japanese Society of Hepato-Biliary-Pancreatic Surgery.

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Auteurs

Masakazu Hashimoto (M)

Department of Gastroenterological Surgery, Hiroshima Prefectural Hospital, Hiroshima, Japan.
Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Tsuyoshi Kobayashi (T)

Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Masahiro Ohira (M)

Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Sho Okimoto (S)

Department of Surgery, Chugoku Rosai Hospital, Kure, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Tomoyuki Abe (T)

Department of Surgery, JA Onomichi General Hospital, Onomichi, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Masashi Inoue (M)

Department of Surgery, National Hospital Organization Higashihiroshima Medical Center, Higashihiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Takashi Onoe (T)

Department of Surgery, National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Kure, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Naruhiko Honmyo (N)

Department of Surgery, Hiroshima City North Medical Center, Asa Citizens Hospital, Hiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Shintaro Kuroda (S)

Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Hideki Ohdan (H)

Department of Gastroenterological and Transplant Surgery, Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima University, Hiroshima, Japan.
HiSCO: Hiroshima Surgical study group of Clinical Oncology, Hiroshima, Japan.

Classifications MeSH