Conversion Hepatectomy for Huge Hepatocellular Carcinoma With Arterioportal Shunt After Chemoembolization and 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
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

5695-5701

Informations de copyright

Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Nobutaka Sato (N)

Department of Surgery, Yamaga City Medical Center, Kumamoto, Japan.

Toru Beppu (T)

Department of Surgery, Yamaga City Medical Center, Kumamoto, Japan tbeppu@yamaga-mc.jp.

Koichi Kinoshita (K)

Department of Surgery, Yamaga City Medical Center, Kumamoto, Japan.

Hideaki Yuki (H)

Department of Radiology, Yamaga City Medical Center, Kumamoto, Japan.

Koichi Suyama (K)

Department of Medical Oncology, Yamaga City Medical Center, Kumamoto, Japan.

Suguru Chiyonaga (S)

Department of Gastroenterology, Yamaga City Medical Center, Kumamoto, Japan.

Toshihiko Motohara (T)

Department of Gastroenterology, Yamaga City Medical Center, Kumamoto, Japan.

Yoshihiko Komohara (Y)

Department of Cell Pathology, Graduate School of Medicine, Kumamoto University, Kumamoto, Japan.

Akio Hara (A)

Internal Medicine, Yamaga Chuo Hospital, Kumamoto, Japan.

Shinichi Akahoshi (S)

Department of Surgery, Yamaga City Medical Center, Kumamoto, Japan.

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Classifications MeSH