| Literature DB >> 31570469 |
Nobutaka Sato1, Toru Beppu2, Koichi Kinoshita1, Hideaki Yuki3, Koichi Suyama4, Suguru Chiyonaga5, Toshihiko Motohara5, Yoshihiko Komohara6, Akio Hara7, Shinichi Akahoshi1.
Abstract
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. CopyrightEntities:
Keywords: Arterioportal shunt; chemoembolization; conversion hepatectomy; hepatocellular carcinoma; lenvatinib therapy
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Year: 2019 PMID: 31570469 DOI: 10.21873/anticanres.13768
Source DB: PubMed Journal: Anticancer Res ISSN: 0250-7005 Impact factor: 2.480