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Controlling Major Portal Vein Invasion Progression during Lenvatinib Treatment by Carbon-Ion Radiotherapy in Patients with Advanced Hepatocellular Carcinoma

Authors :
Ryoi Yoshida
Keisuke Koroki
Hirokazu Makishima
Sadahisa Ogasawara
Takamasa Ishino
Keita Ogawa
Miyuki Nakagawa
Kisako Fujiwara
Hidemi Unozawa
Terunao Iwanaga
Naoto Fujita
Takafumi Sakuma
Hiroaki Kanzaki
Kazufumi Kobayashi
Naoya Kanogawa
Soichiro Kiyono
Masato Nakamura
Takayuki Kondo
Tomoko Saito
Ryo Nakagawa
Eiichiro Suzuki
Yoshihiko Ooka
Shingo Nakamoto
Akinobu Tawada
Tetsuhiro Chiba
Makoto Arai
Takashi Kaneko
Masaru Wakatsuki
Jun Kato
Hiroshi Tsuji
Naoya Kato
Source :
Case Reports in Oncology, Vol 14, Iss 2, Pp 1103-1110 (2021)
Publication Year :
2021
Publisher :
Karger Publishers, 2021.

Abstract

Macrovascular invasion (MVI), including portal vein tumor thrombosis (PVTT), is strongly associated with poor prognosis in patients with hepatocellular carcinoma (HCC). While recommended standard treatment for patients with advanced HCC is systemic therapy, various treatment approaches, including resection, transarterial chemoembolization, and radiation, have been empirically suggested to improve prognosis by eliminating or controlling MVI. Herein, we report our experience of a case with advanced HCC where MVI was controlled by carbon-ion radiotherapy (CIRT) while on systemic therapy, resulting in a prolonged survival. A female patient with HCC in her early 60s had multiple intrahepatic lesions (maximum 60 mm in diameter) with PVTT. The PVTT of this patient had reached the main trunk of the portal vein despite the use of lenvatinib. The other intrahepatic lesions of the patient, except PVTT, had been controlled by lenvatinib. Therefore, hoping to control PVTT, we attempted CIRT. The patient resumed lenvatinib therapy after the irradiation. During lenvatinib re-treatment, no evident progression of PVTT was observed in the patient.

Details

Language :
English
ISSN :
16626575
Volume :
14
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Case Reports in Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.26491db54d54c3589460f579d52e795
Document Type :
article
Full Text :
https://doi.org/10.1159/000517440