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apatinib + doxorubicin + ifosfamide
- Development stage
- Phase 2
- Lead developer
- Sun Yat-sen University
- Modality
- Small Molecules
- Administration
- Oral, Intravenous
01
Overview
This combination therapy consists of apatinib (apatinib mesylate), doxorubicin, and ifosfamide, and is being investigated for the treatment of advanced or metastatic soft tissue sarcoma (STS). Apatinib is a small molecule tyrosine kinase inhibitor that selectively targets vascular endothelial growth factor receptor-2 (VEGFR-2), thereby inhibiting tumor angiogenesis. Doxorubicin is an anthracycline antibiotic that acts as a cytotoxic agent by intercalating into DNA and inhibiting topoisomerase II, leading to DNA damage and cell death. Ifosfamide is a nitrogen mustard alkylating agent that cross-links DNA, interfering with replication and transcription. This triplet regimen, notably studied at Sun Yat-sen University Cancer Center, aims to enhance therapeutic efficacy in sarcoma subtypes by combining targeted anti-angiogenic effects with standard cytotoxic chemotherapy.
- Other names
- Apatinib Mesylate combined with Doxorubicin and IfosfamideApatinib + Doxorubicin + Ifosfamide in Advanced STS
02
Targets
DNATOP2A (DNA topoisomerase II)VEGFR2 (Vascular endothelial growth factor receptor 2)
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