Drug intelligence / Profile preview

BFM chemotherapy + dasatinib + ponatinib

Development stage
Unknown
Lead developer
University of Michigan Rogel Cancer Center
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules, Recombinant Proteins and Enzymes
Administration
Oral, Intravenous, Intrathecal
01

Overview

This therapeutic regimen is a multi-agent combination therapy being evaluated by the University of Michigan Rogel Cancer Center for the treatment of adults with Philadelphia Chromosome-Positive (Ph+) Acute Lymphoblastic Leukemia (ALL). The regimen utilizes a pediatric-inspired Berlin-Frankfurt-Münster (BFM) chemotherapy backbone, which includes a diverse array of cytotoxic agents such as daunorubicin, vincristine, pegaspargase, cyclophosphamide, and methotrexate, integrated with the tyrosine kinase inhibitors (TKIs) dasatinib and ponatinib. The Phase II study (NCT03501368) aims to improve clinical outcomes in adult Ph+ ALL patients by combining intensive chemotherapy with continuous TKI administration, alternating between dasatinib and ponatinib to target the BCR-ABL1 fusion protein while managing overlapping toxicities. The regimen also incorporates rituximab for CD20-positive disease and intrathecal chemotherapy for central nervous system prophylaxis.

Other names
BFM Regimen Plus TKIBFM Regimen Plus TKI in Adult Ph+ ALLpediatric-inspired BFM chemotherapy with dasatinib and ponatinib
02

Targets

ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)CSK (C-terminal Src kinase)ERBB2 (Erb-b2 receptor tyrosine kinase 2)FLT3 (Fms related receptor tyrosine kinase 3)LCK (Proto-oncogene tyrosine-protein kinase Lck)LYN (LYN proto-oncogene, Src family tyrosine kinase)TGFBR1CD20 (B-lymphocyte antigen CD20)DNADNA polymerase familyDHFR (Dihydrofolate reductase)GR (Glucocorticoid receptor)TUBB (Tubulin (alpha and beta subunits))

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