Effects of Short-Term Lenvatinib Administration Prior to Transarterial Chemoembolization for Hepatocellular Carcinoma

Author:

Tachiiri Tetsuya1ORCID,Minamiguchi Kiyoyuki1ORCID,Taiji Ryosuke1ORCID,Sato Takeshi1,Toyoda Shohei1,Matsumoto Takeshi1,Chanoki Yuto1,Kunichika Hideki1ORCID,Yamauchi Satoshi1ORCID,Shimizu Sho1,Nishiofuku Hideyuki1,Marugami Nagaaki1,Tsuji Yuki2,Namisaki Tadashi2ORCID,Yoshiji Hitoshi2,Tanaka Toshihiro1ORCID

Affiliation:

1. Department of Diagnostic and Interventional Radiology, Nara Medical University, Kashihara 634-8522, Japan

2. Department of Gastroenterology, Nara Medical University, Kashihara 634-8522, Japan

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.

Publisher

MDPI AG

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