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rituximab + methotrexate + cytarabine + dexamethasone

Development stage
Preclinical
Lead developer
Genentech
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral, Intrathecal
01

Overview

This is a four-drug combination chemotherapy regimen consisting of rituximab (a monoclonal antibody targeting CD20), methotrexate (an antimetabolite and antifolate agent), cytarabine (an antimetabolite), and dexamethasone (a synthetic glucocorticoid). The combination is primarily used as first-line treatment for primary central nervous system lymphoma (PCNSL), particularly in immunocompetent patients. Rituximab targets the CD20 antigen on B-cells, leading to their destruction via immune-mediated mechanisms. Methotrexate inhibits dihydrofolate reductase, blocking DNA synthesis; cytarabine inhibits DNA polymerase, impairing DNA replication; and dexamethasone exerts anti-inflammatory and lympholytic effects. The addition of rituximab to the methotrexate-cytarabine-dexamethasone backbone has been shown to increase complete remission rates without significantly increasing serious toxicities[1][2][3][6].

Other names
RMAD regimenR-MAD regimen
02

Targets

GR (Glucocorticoid receptor)CD20 (B-lymphocyte antigen CD20)POLA1 (DNA polymerase alpha)DHFR (Dihydrofolate reductase)

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