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QL1706 + eribulin + anlotinib
- Development stage
- Unknown
- Lead developer
- Qilu Pharmaceutical
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
- Administration
- Intravenous, Oral
01
Overview
QL1706 + eribulin + anlotinib is a multimodal combination therapy regimen being investigated for the treatment of advanced or metastatic soft tissue sarcoma. The regimen consists of **QL1706 (epalrotokewali)**, a bifunctional antibody that simultaneously targets programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4); **eribulin**, a non-taxane microtubule dynamics inhibitor; and **anlotinib**, a multi-targeted tyrosine kinase inhibitor that inhibits VEGFR1/2/3, FGFR1-4, PDGFR alpha/beta, and c-Kit. In clinical study contexts, such as the RITEA trial led by Fudan University, this combination is often administered alongside hypofractionated radiotherapy. The strategy aims to leverage the synergistic effects of dual checkpoint blockade, cytotoxic chemotherapy, and anti-angiogenic targeted therapy to improve outcomes in patients who have failed standard prior treatments.
- Other names
- Epalrotokewali + eribulin + anlotinibRITEA regimenQL1706 + Eribulin + Anlotinib + Radiotherapy
02
Targets
FGFR4 (Fibroblast growth factor receptor 4)PDCD1 (Programmed cell death protein 1 receptor)PDGFRA (Platelet-derived growth factor receptor alpha)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)FGFR3 (Fibroblast growth factor receptor 3)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)TUBB (Tubulin (alpha and beta subunits))KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)
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