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apatinib + camrelizumab + docetaxel + S-1

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

apatinib + camrelizumab + docetaxel + S-1 is a multi-drug combination regimen being investigated for the first-line treatment of metastatic gastric adenocarcinoma and gastroesophageal junction (GEJ) adenocarcinoma. This regimen integrates apatinib, a small molecule tyrosine kinase inhibitor that selectively targets vascular endothelial growth factor receptor 2 (VEGFR-2) to inhibit tumor angiogenesis, with camrelizumab, a humanized monoclonal antibody that inhibits the programmed cell death protein 1 (PD-1) checkpoint to enhance anti-tumor immunity. These targeted agents are administered alongside a chemotherapy backbone consisting of docetaxel, a taxane that disrupts microtubule function, and S-1, an oral fluoropyrimidine combination. The regimen is currently being evaluated in clinical trials, such as the HCCSC G05 trial led by investigator Zhou Fuxiang, to determine if the integration of anti-angiogenic therapy and immunotherapy with standard chemotherapy improves clinical outcomes in advanced gastric cancers.

Other names
Apatinib plus Camrelizumab combined with Docetaxel and S1
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TS (Thymidylate synthase)VEGFR2 (Vascular endothelial growth factor receptor 2)TUBB (Tubulin (alpha and beta subunits))

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