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rituximab + ifosfamide + carboplatin + etoposide + mesna + filgrastim

Development stage
Unknown
Lead developer
Memorial Sloan Kettering Cancer Center
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

Rituximab + ifosfamide + carboplatin + etoposide (VP-16) + mesna + G-CSF is a dose-escalated chemoimmunotherapy regimen, often referred to as R-ICEesc or augmented R-ICE. Developed by Memorial Sloan Kettering Cancer Center, it is primarily used as a second-line salvage therapy for patients with primary refractory or relapsed aggressive B-cell non-Hodgkin lymphomas (NHL), such as diffuse large B-cell lymphoma (DLBCL), prior to autologous stem cell transplantation (ASCT). The regimen combines the anti-CD20 monoclonal antibody rituximab with the ICE chemotherapy backbone (ifosfamide, carboplatin, and etoposide). Mesna is included as a uroprotective agent to mitigate ifosfamide-induced hemorrhagic cystitis, and G-CSF is administered to support bone marrow recovery and facilitate peripheral blood progenitor cell mobilization.

Other names
Dose Augmented R-ICEDose-escalated R-ICERituximab + ICE + Mesna + G-CSF
02

Targets

CD20 (B-lymphocyte antigen CD20)TOP2A (DNA topoisomerase II)CSF3R (Granulocyte colony-stimulating factor receptor)DNA

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