伦瓦提尼
细胞毒性T细胞
医学
肝细胞癌
索拉非尼
肿瘤科
癌症研究
内科学
癌
生物
体外
生物化学
作者
Toshimoto Yamada,Naoto Fujiwara,Naoto Kubota,Yuki Matsushita,Takuma Nakatsuka,Shigeyuki Kurosaki,Tatsuya Minami,Ryosuke Tateishi,Akihiko Ichida,Junichi Arita,Kiyoshi Hasegawa,Kazuhiko Koike,Mitsuhiro Fujishiro,Hayato Nakagawa
标识
DOI:10.1097/hc9.0000000000000209
摘要
Background: Lenvatinib was expected to enhance the effect of immune checkpoint inhibitors (ICIs) for unresectable HCC; however, their combination therapy failed to show the synergy in the phase III clinical trial. Methods: To elucidate lenvatinib-induced molecular modulation, we performed bulk RNA-sequencing and digital spatial profiling of 5 surgically resected human HCC specimens after lenvatinib treatment and 10 matched controls without any preceding therapy. Findings: Besides its direct antitumor effects, lenvatinib recruited cytotoxic GZMK+CD8 T cells in intratumor stroma by CXCL9 from tumor-associated macrophages, suggesting that lenvatinib-treated HCC is in the so-called excluded condition that can diminish ICI efficacy.
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