The beneficial impact of metabolic dysfunction-associated fatty liver disease on lenvatinib treatment in patients with non-viral hepatocellular carcinoma.

hepatocellular carcinoma lenvatinib metabolic dysfunction-associated fatty liver disease non-viral hepatoma survival

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:
Feb 2023
Historique:
revised: 14 09 2022
received: 17 07 2022
accepted: 15 09 2022
pubmed: 24 9 2022
medline: 24 9 2022
entrez: 23 9 2022
Statut: ppublish

Résumé

Lenvatinib is used to treat advanced hepatocellular carcinoma (HCC). Metabolic dysfunction-associated fatty liver disease (MAFLD) is becoming a major etiology of HCC. We aimed to evaluate the impact of MAFLD on the efficacy of lenvatinib. We enrolled 320 patients with HCC who were treated with lenvatinib. All patients were classified into the MAFLD (n = 155) and non-MAFLD (n = 165) groups. Independent factors for overall survival (OS) were analyzed. In the stratification analysis, HCC was categorized as non-viral (n = 115) or viral HCC (n = 205). The OS rate was significantly higher in the MAFLD group than in the non-MAFLD group (median 21.1 vs. 15.1 months, p = 0.002). Multivariate analysis demonstrated that, in addition to albumin-bilirubin grade and Barcelona Clinic Liver Cancer stage, MAFLD was identified as an independent factor for OS (HR 0.722, 95% CI 0.539-0.966, p = 0.028). In the stratification analysis, the OS rate was significantly higher in the MAFLD group than in the non-MAFLD group among patients with non-viral HCC (median 21.1 vs. 15.1 months, p = 0.002), but not in patients with viral HCC. Furthermore, MAFLD was an independent negative risk factor for OS in patients with non-viral HCC (HR 0.506, 95% CI 0.297-0.864, P < 0.01). However, MAFLD was not an independent factor for OS in patients with viral HCC. MAFLD was a beneficial factor for survival in patients with HCC treated with lenvatinib. Moreover, the better OS of the MAFLD group was more pronounced in patients with non-viral HCC. Lenvatinib may be a suitable agent for patients with non-viral HCC and MAFLD.

Identifiants

pubmed: 36149726
doi: 10.1111/hepr.13843
doi:

Types de publication

Journal Article

Langues

eng

Pagination

104-115

Subventions

Organisme : Japan Agency for Medical Research and Development
ID : JP22fk0210090

Informations de copyright

© 2022 Japan Society of Hepatology.

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Auteurs

Shigeo Shimose (S)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Atsushi Hiraoka (A)

Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan.

Andrea Casadei-Gardini (A)

Department of Medical Oncology, IRCCS San Raffaele Hospital, Milan, Italy.

Tsubasa Tsutsumi (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Dan Nakano (D)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Hideki Iwamoto (H)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Iwamoto Internal Medical Clinic, Kitakyusyu, Japan.

Fujimasa Tada (F)

Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan.

Margherita Rimini (M)

Division of Oncology, Department of Oncology and Hematology, University of Modena and Reggio Emilia, Modena, Italy.

Masatoshi Tanaka (M)

Clinical Research Center, Yokokura Hospital, Miyama, Fukuoka, Japan.

Takuji Torimura (T)

Department of Gastroenterology, Omuta City Hospital, Omuta, Japan.

Hideya Suga (H)

Department of Gastroenterology and Hepatology, Yanagawa Hospital, Yanagawa, Japan.

Hideko Ohama (H)

Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan.

Valentina Burgio (V)

Department of Medical Oncology, IRCCS San Raffaele Hospital, Milan, Italy.

Takashi Niizeki (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Etsuko Moriyama (E)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Hiroyuki Suzuki (H)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Tomotake Shirono (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Yu Noda (Y)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Naoki Kamachi (N)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Masahito Nakano (M)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Ryoko Kuromatsu (R)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Hironori Koga (H)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Takumi Kawaguchi (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Fukuoka, Japan.

Classifications MeSH