Drug intelligence / Profile preview

endostar + chemotherapy

Development stage
Unknown
Lead developer
Simcere Pharmaceutical Group
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous
01

Overview

Endostar + chemotherapy refers to the combination of recombinant human endostatin (Endostar), an antiangiogenic agent, with standard chemotherapy regimens (such as platinum-based doublet chemotherapy, e.g. cisplatin, paclitaxel, vinorelbine) for cancer treatment. Endostar is a recombinant derivative of endostatin, approved in China for the treatment of non-small cell lung cancer (NSCLC) and studied in other cancers. Endostar inhibits tumor angiogenesis primarily by blocking the vascular endothelial growth factor (VEGF) pathway, specifically by inhibiting VEGF-induced tyrosine phosphorylation and expression of VEGF receptor 2 (VEGFR2/KDR/Flk-1), and modulating related signaling cascades like ERK, p38 MAPK, and AKT. The combination with chemotherapy is intended to enhance antitumor efficacy: Endostar’s normalization of tumor vasculature can increase tumor perfusion and drug delivery, and its hypoxia-modulating effects may enhance radiotherapy or chemotherapeutic sensitivity. Clinical studies in NSCLC and cervical cancer have demonstrated that Endostar plus chemotherapy can improve objective response rates, progression-free survival, and (in some subgroups) overall survival, without substantially increasing adverse events relative to chemotherapy alone.

Other names
recombinant human endostatin + chemotherapy
02

Targets

TUBB (Tubulin (alpha and beta subunits))VEGFR2 (Vascular endothelial growth factor receptor 2)DNA

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