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rituximab + methotrexate + leucovorin + HAART

Development stage
Unknown
Lead developer
National Cancer Institute
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This combination immunochemotherapy regimen was developed by the National Cancer Institute (NCI) specifically for the treatment of AIDS-related primary central nervous system lymphoma (PCNSL). The protocol integrates high-dose methotrexate (HD-MTX), an antifolate small molecule that inhibits dihydrofolate reductase to arrest DNA synthesis, with rituximab, a monoclonal antibody targeting CD20-positive B-cells. Leucovorin is administered as a rescue agent to mitigate systemic toxicity from high-dose methotrexate. Crucially, the regimen is combined with Highly Active Antiretroviral Therapy (HAART) to manage the underlying HIV infection and promote immune reconstitution. This approach was designed to provide effective lymphoma control while minimizing T-cell toxicity in immunocompromised patients with severe CD4+ T-cell lymphopenia.

Other names
R-HD-MTX and HAARTHigh-dose methotrexate with rituximab, leucovorin rescue, and HAARTR-HD-MTX + HAART
02

Targets

DHFR (Dihydrofolate reductase)CD20 (B-lymphocyte antigen CD20)

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