Drug intelligence / Profile preview

cyclophosphamide + doxorubicin + vincristine + prednisone + G-CSF + alemtuzumab

Development stage
Preclinical
Lead developer
National Cancer Institute
Modality
Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Intravenous, Oral, Subcutaneous
01

Overview

This is a multi-agent combination regimen consisting of six drugs: - Cyclophosphamide (an alkylating agent, small molecule chemotherapy) - Doxorubicin (an anthracycline antibiotic, small molecule chemotherapy) - Vincristine (a vinca alkaloid, small molecule chemotherapy) - Prednisone (a synthetic glucocorticoid corticosteroid, small molecule immunosuppressant/anti-inflammatory) - G-CSF (granulocyte colony-stimulating factor; a biologic cytokine that stimulates neutrophil production) - Alemtuzumab (a monoclonal antibody targeting CD52 on lymphocytes) The first four agents are the basis of the CHOP regimen, widely used in non-Hodgkin lymphoma and other hematologic malignancies. These drugs act by interfering with DNA synthesis or mitosis in rapidly dividing cells and by modulating immune responses[1][4][6]. G-CSF is added to reduce neutropenia risk by stimulating white blood cell recovery. Alemtuzumab targets CD52 on B and T lymphocytes for direct cytotoxicity via immune-mediated mechanisms. This specific combination is not standard but may be considered in research or high-risk/refractory settings where additional immunosuppression or cytotoxicity is desired.

Brand names
MabCampathCampath
Other names
CHOP-14 + alemtuzumabAlemtuzumab-CHOPA-CHOPCampath-CHOP
02

Targets

TOP2A (DNA topoisomerase II)CD52 (CD52 Antigen)GR (Glucocorticoid receptor)DNACSF3R (Granulocyte colony-stimulating factor receptor)TUBB (Tubulin (alpha and beta subunits))

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