Drug intelligence / Profile preview

apatinib + chemoradiation

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Implantable Devices → Device-based Delivery → Drug Delivery Systems, Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

Apatinib + chemoradiation refers to the combination of the small molecule tyrosine kinase inhibitor apatinib with standard chemotherapy and radiotherapy regimens. Apatinib is an oral inhibitor that selectively targets vascular endothelial growth factor receptor-2 (VEGFR-2), thereby blocking angiogenesis and inhibiting tumor growth. When combined with chemotherapy or radiotherapy, this regimen aims to enhance anti-tumor efficacy by both direct cytotoxic effects (from chemo/radiation) and antiangiogenic mechanisms (from apatinib). This combination has been studied in several advanced cancers—including gastric cancer, lung adenocarcinoma, pancreatic cancer, breast cancer, and ovarian cancer—where it has shown improved progression-free survival and overall response rates compared to standard therapy alone. The safety profile is generally manageable; common adverse events include hypertension, proteinuria, hand-foot syndrome, fatigue, and hematologic toxicities[1][3][5][7].

Other names
apatinib mesylatechemoradiation
02

Targets

RET (Rearranged during transfection receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)SRC (Proto-oncogene tyrosine-protein kinase Src)

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