Conversion Hepatectomy for Huge Hepatocellular Carcinoma With Arterioportal Shunt After Chemoembolization and Lenvatinib Therapy.
Aged
Biomarkers, Tumor
/ metabolism
Carcinoma, Hepatocellular
/ drug therapy
Chemoembolization, Therapeutic
/ methods
Female
Hepatectomy
/ methods
Humans
Liver Neoplasms
/ drug therapy
Neoplasm Recurrence, Local
/ drug therapy
Phenylurea Compounds
/ therapeutic use
Quinolines
/ therapeutic use
alpha-Fetoproteins
/ metabolism
Arterioportal shunt
chemoembolization
conversion hepatectomy
hepatocellular carcinoma
lenvatinib therapy
Journal
Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
09
08
2019
revised:
22
08
2019
accepted:
28
08
2019
entrez:
2
10
2019
pubmed:
2
10
2019
medline:
8
10
2019
Statut:
ppublish
Résumé
Large tumor size and arterioportal shunt are poor prognostic factors for hepatocellular carcinoma. Lenvatinib is a novel and potent multi-tyrosine kinase inhibitor developed in Japan. A 66-year-old woman with hepatocellular carcinoma and untreated hepatitis C was referred to our hospital. She was judged as unresectable and was treated with four sessions of transarterial chemoembolization; however, the therapeutic effect was unsatisfactory because of major arterioportal shunt. Lenvatinib was sequentially administered for 4 months. Thereafter, we observed tumor shrinkage, complete disappearance of arterioportal shunt, and obvious improvement in liver function. A curative conversion hepatectomy was successfully accomplished. The extremely high levels of tumor markers almost normalized; the pretreatment levels were 1,008,021 ng/ml for alpha-fetoprotein. At 1 year after the primary treatment, the patient has not experienced recurrence. To our knowledge, this is the first case of a patient with initially unresectable hepatocellular carcinoma with arterioportal shunt who underwent conversion hepatectomy after multidisciplinary treatment, including lenvatinib.
Identifiants
pubmed: 31570469
pii: 39/10/5695
doi: 10.21873/anticanres.13768
doi:
Substances chimiques
Biomarkers, Tumor
0
Phenylurea Compounds
0
Quinolines
0
alpha-Fetoproteins
0
lenvatinib
EE083865G2
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
5695-5701Informations de copyright
Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.