Formulation of a triple combination gemcitabine plus romidepsin + cisplatin regimen to efficaciously and safely control triple-negative breast cancer tumor development.
Pawat PattarawatShelby WallaceBianca PfistererAgricola OdoiHwa-Chain Robert WangPublished in: Cancer chemotherapy and pharmacology (2019)
Considering the high costs for developing a new anticancer agent, we used the FDA-approved drugs gemcitabine, romidepsin (is approved for T-cell lymphoma and is under clinical trial for TNBC), and cisplatin to economically formulate an efficacious and safe combination regimen. The highly efficacious gemcitabine plus romidepsin + cisplatin regimen should be poised for efficient translation into clinical trials, ultimately contributing to reduced mortality and improved quality of life for TNBC patients.
Keyphrases
- clinical trial
- end stage renal disease
- locally advanced
- ejection fraction
- newly diagnosed
- phase ii
- chronic kidney disease
- prognostic factors
- drug delivery
- drug administration
- open label
- peritoneal dialysis
- cardiovascular events
- study protocol
- type diabetes
- cardiovascular disease
- risk factors
- double blind
- phase iii
- patient reported