An exploratory human study of superstable homogeneous lipiodol-indocyanine green formulation for precise surgical navigation in liver cancer.
An exploratory human study of superstable homogeneous lipiodol-indocyanine green formulation for precise surgical navigation in liver cancer.
复制标题
DOI:
10.1002/btm2.10404
复制
发表时间:
2023-03
影响因子:
7.4
通讯作者:
Liu, Gang
中科院分区:
文献类型:
--
作者:
He, Pan;Xiong, Yongfu;Luo, Bin;Liu, Jianming;Zhang, Yang;Xiong, Yu;Su, Song;Fang, Cheng;Peng, Yisheng;Cheng, Hongwei;Chu, Chengchao;Mao, Jingsong;Li, Jingdong;Li, Bo;Yin, Zhenyu;Tian, Jie;Liu, Gang
The clinical applications of transcatheter arterial embolization (TAE) conversion therapy combined with hepatectomy have been severely restricted by ill‐defined tumoral boundaries and miniscule hidden lesions. Fluorescent surgical navigation is a promising method for overcoming these barriers. However, sufficient delivery of the fluorescent probe into the tumor region after long‐term TAE is challenging due to blockade of the tumor‐supplying artery. Here, a super‐stable homogeneous intermix formulating technology (SHIFT) to physically mix lipiodol and indocyanine green (ICG) formulation (SHIFT and ICG) for fluorescent surgical navigation after long‐term TAE conversion therapy is provided. Through the retrospective study of 45 clinical liver cancer patients, it is found that SHIFT and ICG formulation have excellent tumor deposition effect and safety. During surgical resection after long‐term TAE conversion therapy, SHIFT and ICG could clearly identify in real time the full tumor regions and boundaries and had a high signal‐to‐normal tissues ratio—even the indistinguishable satellite lesions could be identified with a strong fluorescence intensity. Meanwhile, SHIFT and ICG could improve operative, anesthetic, and postoperative variables associated with postoperative complications. This simple and effective SHIFT could provide precise fluorescent navigation for surgical resection following long‐term embolization therapy in clinical practice and has great potential for a translational pipeline.
登录
查看更多内容
影响因子:
3.8
作者:
Okumura, Shinya;Goumard, Claire;Scatton, Olivier
通讯作者:
Scatton, Olivier
影响因子:
6.2
作者:
Ishizawa, Takeaki;Fukushima, Noriyoshi;Kokudo, Norihiro
通讯作者:
Kokudo, Norihiro
DOI:
10.1007/s00464-014-3895-x
发表时间:
2015-07
影响因子:
3.1
作者:
Boni, Luigi;David, Giulia;Mangano, Alberto;Dionigi, Gianlorenzo;Rausei, Stefano;Spampatti, Sebastiano;Cassinotti, Elisa;Fingerhut, Abe
通讯作者:
Fingerhut, Abe
影响因子:
28.1
作者:
Hu, Zhenhua;Fang, Cheng;Tian, Jie
通讯作者:
Tian, Jie
影响因子:
2
作者:
Goto, Yuichi;Hisaka, Toru;Okuda, Koji
通讯作者:
Okuda, Koji