Drug intelligence / Profile preview

alemtuzumab + fludarabine + cyclophosphamide + total body irradiation

Development stage
Unknown
Lead developer
University of Texas MD Anderson Cancer Center
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

This preparative regimen, also known as a conditioning regimen, was developed and evaluated by the M.D. Anderson Cancer Center for patients with peripheral T-cell lymphoma (PTCL) undergoing allogeneic stem cell transplantation. It is a reduced-intensity conditioning (RIC) protocol designed to facilitate donor engraftment and provide anti-lymphoma activity while minimizing the toxicities associated with traditional high-dose conditioning. The regimen consists of alemtuzumab (Campath-1H), a monoclonal antibody that targets the CD52 antigen to provide potent in vivo T-cell depletion; fludarabine, a purine analog that inhibits DNA synthesis; cyclophosphamide, an alkylating agent that causes DNA cross-linking; and low-dose total body irradiation (2 Gy). This combination aims to achieve a balance between sufficient immunosuppression to prevent graft rejection and graft-versus-host disease (GVHD) and the preservation of a graft-versus-lymphoma effect.

Other names
Campath-1H + fludarabine + cyclophosphamide + TBIAlemtuzumab-based reduced intensity conditioningMDACC PTCL Allogeneic Preparative Regimen
02

Targets

CD52 (CD52 Antigen)

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