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PD-1 inhibitor + anlotinib

Development stage
Unknown
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous (for The Monoclonal Antibody), Oral (for Anlotinib)
01

Overview

PD-1 inhibitor + anlotinib is a combination therapy consisting of a programmed cell death protein 1 (PD-1) immune checkpoint inhibitor and anlotinib, a small molecule multi-target tyrosine kinase inhibitor. The PD-1 inhibitors used in this combination are typically monoclonal antibodies such as sintilimab or penpulimab, which block the interaction between PD-1 on T cells and its ligands, thereby enhancing anti-tumor immune responses. Anlotinib inhibits multiple receptor tyrosine kinases involved in tumor angiogenesis and proliferation, including VEGFR, FGFR, and PDGFR. This combination has been investigated primarily for advanced cancers such as non-small cell lung cancer (NSCLC), hepatocellular carcinoma (HCC), neuroendocrine carcinoma, and other solid tumors. Clinical studies have shown that the regimen can improve objective response rates and progression-free survival compared to monotherapy or standard treatments[2][4][5][6]. The typical administration involves intravenous infusion of the PD-1 antibody every three weeks combined with oral anlotinib given in cycles.

Other names
PD-1抑制剂 + 安罗替尼
02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)PDCD1 (Programmed cell death protein 1 receptor)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)FGFR3 (Fibroblast growth factor receptor 3)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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