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Please use this identifier to cite or link to this item: http://hdl.handle.net/10564/4419

Title: Effects of Short-Term Lenvatinib Administration Prior to Transarterial Chemoembolization for Hepatocellular Carcinoma
Other Titles: 肝細胞癌に対する肝動脈化学塞栓術前の短期間レンバチニブ投与の有効性
Authors: Tachiiri, Tetsuya
Minamiguchi, Kiyoyuki
Taiji, Ryosuke
Sato, Takeshi
Toyoda, Shohei
Matsumoto, Takeshi
Chanoki, Yuto
Kunichika, Hideki
Yamauchi, Satoshi
Shimizu, Sho
Nishiofuku, Hideyuki
Marugami, Nagaaki
Tsuji, Yuki
Namisaki, Tadashi
Yoshiji, Hitoshi
Tanaka, Toshihiro
Keywords: combined therapy
hepatocellular carcinoma
lenvatinib
transarterial chemoembolization
Issue Date: Apr-2024
Publisher: MDPI
Citation: Cancers. 2024 Apr, vol.16, no.9, article no.1624
Abstract: Aim: Transarterial chemoembolization (TACE) combined with lenvatinib, employing a 4-day lenvatinib administration followed by TACE without an interval (short-term LEN-TACE), was performed for hepatocellular carcinoma (HCC). The aim was to assess tumor hemodynamics following the 4-day lenvatinib and to evaluate the treatment outcomes after the short-term LEN-TACE. Methods: 25 unresectable HCC patients received this combined therapy. Lenvatinib (4-12 mg) was administrated for 4 days prior to TACE. Perfusion CT scans were obtained before and after the lenvatinib administration. Either cTACE (76%) or DEB-TACE (24%) were performed. Results: intra-tumor blood flow significantly decreased after the 4-day lenvatinib (p < 0.05). The TACE procedure was successful with no severe adverse events in all patients. The overall complete response (CR) rate was 75% (cTACE 84%, DEB-TACE 40%). The lipiodol-washout ratio between 1 week and 4 months after cTACE correlated with the arterial flow reduction ratio by lenvatinib prior to TACE (r = -0.55). The 12-month progression-free survival (PFS) rate was 75.0%. Conclusions: The short-term LEN-TACE is feasible and safe, demonstrating promising outcomes with a high CR ratio, contributing to lipiodol retention in the tumor after cTACE, and extended PFS. To confirm the advantages of this treatment protocol, a prospective clinical trial is mandatory.
Description: 権利情報:© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
URI: http://hdl.handle.net/10564/4419
ISSN: 2072-6694
DOI: https://doi.org/10.3390/cancers16091624
Academic Degrees and number: 24601甲第943号
Degree-granting date: 2024-12-26
Degree name: 博士(医学)
Degree-granting institutions: 奈良県立医科大学
Appears in Collections:2024年度

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