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rituximab + temsirolimus + dexamethasone + cytarabine + cisplatin

Development stage
Phase 2
Lead developer
Pfizer
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

This drug is a combination chemotherapy regimen consisting of five agents: rituximab (a monoclonal antibody targeting CD20), temsirolimus (an mTOR inhibitor), dexamethasone (a synthetic glucocorticoid corticosteroid), cytarabine (an antimetabolite chemotherapeutic agent), and cisplatin (a platinum-based DNA crosslinking agent). This specific combination, known as the STORM regimen, has been studied primarily in relapsed or refractory diffuse large B-cell lymphoma. The mechanism of action involves multiple pathways: - Rituximab targets CD20 on B-cells, leading to cell lysis via immune-mediated mechanisms. - Temsirolimus inhibits the mammalian target of rapamycin (mTOR) pathway, suppressing tumor cell growth and proliferation. - Dexamethasone exerts anti-inflammatory and lympholytic effects through glucocorticoid receptor agonism. - Cytarabine interferes with DNA synthesis by acting as a pyrimidine analog. - Cisplatin forms DNA crosslinks that inhibit replication and transcription. The STORM regimen was evaluated in a phase II clinical trial for patients with relapsed or refractory diffuse large B-cell lymphoma. The addition of temsirolimus to the standard R-DHAP protocol showed promising activity with manageable toxicity[1][2][4][5].

Other names
STORM regimen
02

Targets

CD20 (B-lymphocyte antigen CD20)DNAFKBP1AGR (Glucocorticoid receptor)mTOR (Mammalian target of rapamycin kinase)

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