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Lenvatinib recruits cytotoxic GZMK+CD8 T cells in hepatocellular carcinoma

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 an...

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Detalles Bibliográficos
Autores principales: Yamada, Tomoharu, Fujiwara, Naoto, Kubota, Naoto, Matsushita, Yuki, Nakatsuka, Takuma, Kurosaki, Shigeyuki, Minami, Tatsuya, Tateishi, Ryosuke, Ichida, Akihiko, Arita, Junichi, Hasegawa, Kiyoshi, Koike, Kazuhiko, Fujishiro, Mitsuhiro, Nakagawa, Hayato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351952/
https://www.ncbi.nlm.nih.gov/pubmed/37471053
http://dx.doi.org/10.1097/HC9.0000000000000209
Descripción
Sumario: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.