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mitoxantrone + cyclophosphamide + fludarabine + rituximab + GM-CSF

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Intravenous, Subcutaneous, Oral
01

Overview

This regimen is a multi-agent chemoimmunotherapy combination used primarily in the treatment of chronic lymphocytic leukemia (CLL). It combines four drugs—mitoxantrone (a topoisomerase II inhibitor), cyclophosphamide (an alkylating agent), fludarabine (a purine analog antimetabolite), and rituximab (a monoclonal antibody targeting CD20)—with granulocyte-macrophage colony-stimulating factor (GM-CSF, a cytokine that stimulates white blood cell production). The addition of rituximab to the chemotherapy backbone has been shown to significantly improve response rates in CLL. GM-CSF is included to support hematopoiesis and reduce infection risk during myelosuppressive therapy. This combination has demonstrated high overall and complete response rates, including minimal residual disease-negative responses, with acceptable toxicity profiles in clinical trials for previously untreated CLL[1][2][3][4].

Other names
granulocyte-macrophage colony-stimulating factor
02

Targets

CSF2R (Granulocyte-macrophage colony-stimulating factor receptor)TOP2B (DNA topoisomerase II beta)CD20 (B-lymphocyte antigen CD20)DNA-directed primase/polymerase protein (PrimPol)RNR (Ribonucleotide reductase)DNA polymerase familyDNATOP2A (DNA topoisomerase II)LIG1 (DNA ligase 1)

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