Drug intelligence / Profile preview

MA-BUCY2

Development stage
Unknown
Lead developer
First Affiliated Hospital of Xi'an Jiaotong University
Modality
Small Molecules, Liposomes → Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

MA-BUCY2 is an intensified conditioning regimen developed by the First Affiliated Hospital of Xi'an Jiaotong University for patients with high-risk acute myeloid leukemia (AML) undergoing haploidentical hematopoietic stem cell transplantation (haplo-HSCT). This regimen is a modification of the standard BUCY2 (Busulfan and Cyclophosphamide) protocol, incorporating mitoxantrone liposome, cytarabine (Ara-C), semustine (me-CCNU), and antithymocyte globulin (ATG). The addition of mitoxantrone liposome and high-dose cytarabine is intended to enhance the anti-leukemic effect and reduce the risk of relapse in high-risk populations. The regimen's mechanism of action involves a multi-pronged approach: DNA alkylation (via busulfan, cyclophosphamide, and semustine), DNA intercalation and topoisomerase II inhibition (via mitoxantrone), and DNA synthesis inhibition (via cytarabine), while ATG provides the necessary immunosuppression to prevent graft rejection and graft-versus-host disease (GVHD).

Other names
MA-BUCY2 regimenMA-BUCY-2 regimenMA-BUCY 2 regimenMA-BUCY2 protocolMA-BUCY-2 protocolMA-BUCY 2 protocolMA-BUCY2 conditioning regimenMA-BUCY-2 conditioning regimenMA-BUCY 2 conditioning regimen
02

Targets

DNA polymerase familyTOP2A (DNA topoisomerase II)DNA

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