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dasatinib + bevacizumab + paclitaxel + methylnaltrexone
- Development stage
- Unknown
- Lead developer
- University of Texas MD Anderson Cancer Center
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
- Administration
- Intravenous, Oral
01
Overview
This is an investigational combination therapy evaluated in a Phase I trial (NCT01015222) led by the M.D. Anderson Cancer Center. The regimen consists of metronomic (low-dose, frequent) paclitaxel, dasatinib (a BCR-ABL and SRC family tyrosine kinase inhibitor), and bevacizumab (a VEGF-targeting monoclonal antibody), with or without the addition of methylnaltrexone. The study targeted patients with advanced or metastatic malignancies refractory to standard treatments. The rationale behind the combination is to leverage the anti-angiogenic effects of metronomic chemotherapy and bevacizumab alongside the SRC inhibition provided by dasatinib to overcome resistance and inhibit tumor growth and metastasis. Methylnaltrexone was included in specific cohorts to evaluate its potential role in blocking opioid-receptor-mediated signaling that may contribute to tumor progression and angiogenesis.
- Other names
- paclitaxel-M.D. Anderson Cancer Center-advanced cancerMetronomic paclitaxel combination therapyDasatinib + Bevacizumab + Paclitaxel +/- Methylnaltrexone
02
Targets
ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)MOR (Mu opioid receptor)SFK (SRC family kinases)VEGFA (Vascular endothelial growth factor A)TUBB (Tubulin (alpha and beta subunits))
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