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01 奈良県立医科大学 >
012 大学院 >
0122 学位請求論文 >
01221 博士論文(医学) >
2024年度 >
このアイテムの引用には次の識別子を使用してください:
http://hdl.handle.net/10564/4419
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タイトル: | Effects of Short-Term Lenvatinib Administration Prior to Transarterial Chemoembolization for Hepatocellular Carcinoma |
その他のタイトル: | 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 |
著者: | 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 |
キーワード: | combined therapy hepatocellular carcinoma lenvatinib transarterial chemoembolization |
発行日: | 2024年4月 |
出版者: | MDPI |
引用: | Cancers. 2024 Apr, vol.16, no.9, article no.1624 |
抄録: | 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. |
内容記述: | 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 |
学位授与番号: | 24601甲第943号 |
学位授与年月日: | 2024-12-26 |
学位名: | 博士(医学) |
学位授与機関: | 奈良県立医科大学 |
出現コレクション: | 2024年度
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