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Rituximab

Vue déterministe de l'entité source de la LJAM. L'autorité clinique demeure avec les ID de la source cités et l'état d'approbation de l ́examinateur.

IDDRUG-RITUXIMAB
TypeMédicament
Alias
MabTheraRiabni (biosimilaire)RituxanRuxience (biosimilaire)Truxima (biosimilaire)Ритуксимаб
Étatreviewed 2026-04-26 | pending_clinical_signoff
MaladiesDIS-B-ALL DIS-BURKITT DIS-CLL DIS-DLBCL-NOS DIS-FL DIS-HCL DIS-HCV-MZL DIS-HGBL-DH DIS-MCL DIS-NLPBL DIS-NODAL-MZL DIS-PCNSL DIS-PMBCL DIS-PTLD DIS-SPLENIC-MZL DIS-T-ALL DIS-WM
SourcesSRC-ESMO-MZL-2024 SRC-NCCN-BCELL-2025

Faits sur les drogues

Catégoriemonoclonal_antibody — anti-CD20 chimeric IgG1κ
MécanismeChimeric (mouse-human) monoclonal antibody binding the CD20 antigen on B lymphocytes (pre-B through mature B; sparing pro-B and plasma cells). Depletes CD20+ B cells via three mechanisms: complement-dependent cytotoxicity (CDC, dominant in CLL), antibody-dependent cellular cytotoxicity (ADCC, dominant in lymphoma), and direct apoptosis via CD20 cross-linking. Recovery of normal B cells takes 6-12 months after the last dose.
Dose typiqueR-CHOP / R-CVP / R-Bendamustine (DLBCL, FL): 375 mg/m² IV day 1 of each 21- or 28-day cycle × 6-8 cycles. R-monotherapy / FL maintenance: 375 mg/m² IV every 8-12 weeks × 2 years (PRIMA / RESORT schedules). CLL (R-FC, R-Ben): 375 mg/m² IV cycle 1 day 1, then 500 mg/m² IV day 1 cycles 2-6. SC formulation (FL, DLBCL): 1400 mg fixed-dose SC over ~5 minutes from cycle 2 onward (after first IV dose for tolerability).
Ukraine enregistréeVrai
NSZU rembourséVrai
Ukraine vérifiée pour la dernière fois2026-04-27

Avertissements

Notes

Foundation anti-CD20 therapy in B-cell lymphomas. Premedication (acetaminophen + diphenhydramine ± methylprednisolone) before each infusion; first-dose infusion rate escalation per protocol (50 mg/h start, doubled q30min to max 400 mg/h). HBV screening (HBsAg + anti-HBc + anti-HBs) is mandatory before first dose; entecavir or tenofovir prophylaxis throughout therapy and ≥12 months post for any HBV-positive serology. SC formulation reduces administration time from 4-6 h to 5-7 minutes and is preferred from cycle 2 onward in FL / DLBCL. For HCV-MZL, reserved for cases not responding to antiviral therapy alone, or aggressive phenotype where immediate cytoreduction is indicated. Biosimilars are clinically interchangeable in UA per НСЗУ guidance.

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Contraindications

Protocole thérapeutique