Drug intelligence / Profile preview

EPOCH-F

Development stage
Unknown
Lead developer
National Cancer Institute
Modality
Small Molecules
Administration
Intravenous, Oral
01

Overview

EPOCH-F is a combination chemotherapy regimen developed as a salvage therapy for multiple myeloma, particularly in patients being considered for reduced-intensity allogeneic hematopoietic stem cell transplantation (RI-alloHSCT). The regimen consists of six drugs administered in specific sequences and dosages: - Etoposide (a topoisomerase II inhibitor) - Prednisone (a glucocorticoid steroid) - Vincristine (Oncovin; a vinca alkaloid that inhibits microtubule formation) - Cyclophosphamide (an alkylating agent) - Doxorubicin (Adriamycin; an anthracycline antibiotic that intercalates DNA and inhibits topoisomerase II) - Fludarabine (a purine analog antimetabolite) The primary goals of the EPOCH-F regimen are to achieve tumor control and deplete host lymphocytes, thereby facilitating donor engraftment prior to RI-alloHSCT. In clinical studies, this regimen has demonstrated manageable toxicity profiles—primarily hematologic—and effective disease control with consistent full donor engraftment in multiple myeloma patients[1].

02

Targets

DNA-directed primase/polymerase protein (PrimPol)TOP2A (DNA topoisomerase II)GR (Glucocorticoid receptor)DNATUBB (Tubulin (alpha and beta subunits))POLA1 (DNA polymerase alpha)

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