Liver Function in Older Patients With Unresectable Hepatocellular Carcinoma After Administration of Lenvatinib.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 07 02 2021
revised: 23 02 2021
accepted: 24 02 2021
entrez: 4 4 2021
pubmed: 5 4 2021
medline: 28 4 2021
Statut: ppublish

Résumé

The age of patients with advanced hepatocellular carcinoma (HCC) eligible for molecular-targeted drug treatment is increasing. We assessed liver function after lenvatinib administration according to age in patients with advanced HCC. In this retrospective, multicenter, observational study, we reviewed the records of patients with HCC who received lenvatinib treatment (March 2018-March 2020). Liver function was measured using the Albumin-Bilirubin Index (ALBI). Of 119 patients, with a median age of 72.0 years, median overall survival was 15.3 months. Overall survival was significantly better in the group which maintained liver function (p=0.02). Older age (≥72 years) was associated with liver-function deterioration within 8 weeks (odds ratio=2.47, 95% confidence interval=1.06-5.75, p=0.035). The ALBI score was significantly higher in the older group at 4 and 8 weeks after lenvatinib administration. Lenvatinib administration was more likely to adversely affect liver function in older patients; dose adjustment should be considered in such patients.

Sections du résumé

BACKGROUND BACKGROUND
The age of patients with advanced hepatocellular carcinoma (HCC) eligible for molecular-targeted drug treatment is increasing. We assessed liver function after lenvatinib administration according to age in patients with advanced HCC.
PATIENTS AND METHODS METHODS
In this retrospective, multicenter, observational study, we reviewed the records of patients with HCC who received lenvatinib treatment (March 2018-March 2020). Liver function was measured using the Albumin-Bilirubin Index (ALBI).
RESULTS RESULTS
Of 119 patients, with a median age of 72.0 years, median overall survival was 15.3 months. Overall survival was significantly better in the group which maintained liver function (p=0.02). Older age (≥72 years) was associated with liver-function deterioration within 8 weeks (odds ratio=2.47, 95% confidence interval=1.06-5.75, p=0.035). The ALBI score was significantly higher in the older group at 4 and 8 weeks after lenvatinib administration.
CONCLUSION CONCLUSIONS
Lenvatinib administration was more likely to adversely affect liver function in older patients; dose adjustment should be considered in such patients.

Identifiants

pubmed: 33813409
pii: 41/4/2025
doi: 10.21873/anticanres.14970
doi:

Substances chimiques

Phenylurea Compounds 0
Quinolines 0
lenvatinib EE083865G2

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2025-2032

Informations de copyright

Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Ryu Sasaki (R)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; r.sasaki@nagasaki-u.ac.jp.

Masanori Fukushima (M)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Masafumi Haraguchi (M)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Satoshi Miuma (S)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Hisamitsu Miyaaki (H)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Masaaki Hidaka (M)

Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Susumu Eguchi (S)

Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Satoshi Matsuo (S)

Gastroenterology and Hepatology, Sasebo City General Hospital, Sasebo, Japan.

Toshihisa Matsuzaki (T)

Gastroenterology and Hepatology, Sasebo City General Hospital, Sasebo, Japan.

Satsuki Hashimoto (S)

Gastroenterology and Hepatology, Japan Community Health Care Organization, Isahaya, Japan.

Kazuo Ohba (K)

Gastroenterology and Hepatology, Japan Community Health Care Organization, Isahaya, Japan.

Yuki Kugiyama (Y)

Clinical Research Center, National Hospital Organization, Omura, Japan.

Hiroshi Yatsuhashi (H)

Clinical Research Center, National Hospital Organization, Omura, Japan.

Hidetaka Shibata (H)

Gastroenterology and Hepatology, Shibata Chokodo Hospital, Shimabara, Japan.

Yasuhide Motoyoshi (Y)

Gastroenterology and Hepatology, Nagasaki Harbor Medical Center, Nagasaki, Japan.

Masaya Shigeno (M)

Gastroenterology and Hepatology, Japanese Red Cross, Nagasaki, Japan.

Shinichi Iwatsu (S)

Gastroenterology and Hepatology, Oita Prefectural Hospital, Oita, Japan.

Yuji Kato (Y)

Gastroenterology and Hepatology, Oita Prefectural Hospital, Oita, Japan.

Noboru Kinoshita (N)

Gastroenterology and Hepatology, Sasebo Chuo Hospital, Sasebo, Japan.

Kazuhiko Nakao (K)

Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

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Classifications MeSH