Table 3b.
In Vivo treatment scheme of PDOX models.
Compounds | Name in the study | Target | Solution for compounds | Treatment scheme in PDOX model |
Route of administration |
---|---|---|---|---|---|
Alvocidib | Flavopiridol | CDK9 kinase inhibitor | 1 mg/mL in 0.2 mL DMSO add 14.8 mL PBS | 5 mg/kg/day ×12 days | i.p. |
Alisertib | MLN8237 | Aurora A Kinase inhibitor | 5 mg/mL in 10% HPBCD/1% sodium bicarbonate | 30 mg/kg/day x 12 days | gavage |
NA | Radiation | DNA | NA | 2 Gy/day x 5 days | In located brain |
Temozolomide | TMZ | Alkylate/methylate DNA | In water | 50 mg/kg/day ×5 day | gavage |
Panobinostat | Panobinostat | HDACi | 2 mg/mL in DMSO (1.3%)/DPBS | 10 mg/kg (5 d on-2 d off) x 2 cycle | i.p. |
Valproic acid | VPA | HDACi | In 0.9% sodium chloride solution | 600 mg/mL x 7 days (1 μl/hr), | Pump |
Suberoylanilide Hydroxamic Acid | SAHA | HDACi | In PBS/DMSO (1:1) | 100 mg/kg, Qd, 2 weeks | i.p. |
Veliparib | ABT888 | PARPi inhibitor | In 2% DMSO | 10μl/g ×5 days, Qd | i.p. |
Cisplatin | Cisplatin | DNA | Sterile water | 5 mL/kg on days 1 and 4 | i.p. |
Seneca Valley Virus | SVV-001 | Oncolytic virus | In PBS | 20μ1*10^8vp/ul for one time | Tail vein |