Oxaliplatin
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.
| ID | DRUG-OXALIPLATIN |
|---|---|
| Type | Médicament |
| Alias | ÉloxatineОксаліплатин |
| État | reviewed 2026-04-26 | pending_clinical_signoff |
| Maladies | DIS-CRC DIS-ESOPHAGEAL DIS-GASTRIC DIS-NK-T-NASAL DIS-PDAC |
| Sources | SRC-ESMO-COLON-2024 SRC-NCCN-COLON-2025 |
Faits sur les drogues
| Catégorie | Agent alkylant de platine (troisième génération; DACH-platine) |
|---|---|
| Mécanisme | Diaminocyclohexane (DACH) platinum compound. Forms intra- and inter- strand platinum-DNA adducts (preferentially N7 of guanine), bulkier than cisplatin/carboplatin adducts and recognized differently by the mismatch-repair machinery — explains partial activity in MMR-deficient tumors. Cumulative dose-dependent peripheral sensory neuropathy is the signature toxicity (acute cold-induced + chronic stocking-glove). Backbone of FOLFOX, CAPOX, FOLFIRINOX, FLOT. |
| Dose typique | FOLFOX (mFOLFOX6): 85 mg/m² IV over 2 h day 1 every 14 d. CAPOX (XELOX): 130 mg/m² IV over 2 h day 1 every 21 d. FOLFIRINOX: 85 mg/m² IV day 1 every 14 d. FLOT (gastric): 85 mg/m² IV day 1 every 14 d. Adjuvant colon (IDEA-supported): 3 months CAPOX or 6 months FOLFOX per stage and risk; cumulative dose target ≤780 mg/m² to limit chronic neuropathy. |
| Ukraine enregistrée | Vrai |
| NSZU remboursé | Vrai |
| Ukraine vérifiée pour la dernière fois | 2026-04-27 |
Avertissements
- Réactions anaphylactiques / anaphylactoïdes (epinephrine, corticostéroïdes, antihistaminiques pour le traitement; augmentation du risque ≥cycle 6)
Notes
Cumulative-dose neuropathy management: stop or de-escalate at Grade 2 functional neuropathy or after ~780-1000 mg/m² regardless. Cold avoidance × 5 days post-dose (gloves, no cold drinks). IDEA trial: 3 vs 6 months adjuvant in stage III colon — for low-risk T1-3 N1, 3 months CAPOX is non-inferior with substantially less neuropathy. Calcium / magnesium infusions for neuropathy prevention NOT supported by N08CB trial — abandoned as standard.
Utilisé par
Protocole thérapeutique
REG-BEMARITUZUMAB-MFOLFOX6- Bemarituzumab + mFOLFOX6 (FORTITUDE-101) — 1L FGFR2b-expression HER2- gaz non positif...REG-CAPOX- CAPOX (XELOX)REG-FLOT- FLOTREG-FOLFIRINOX- FOLFIRINOXREG-FOLFOX- FOLFOX (mFOLFOX6)REG-FOLFOX-BEV- FOLFOX + BevacizumabREG-FOLFOX-CETUX- FOLFOX + CetuximabREG-FOLFOX-NIVO- FOLFOX + NivolumabREG-FOLFOXIRI-BEV- FOLFOXIRI + BevacizumabREG-MFOLFIRINOX- mFOLFIRINOX (FOLFIRINOX modifié, protocole PRODIGE-24)REG-NALIRIFOX- NALIRIFOXREG-P-GEMOX-NK-T- P-GEMOX (pegaspargase + gemcitabine + oxaliplatin) for NK/T-cell nasal lymphomaREG-ZOLBETUXIMAB-CHEMO- Zolbetuximab + mFOLFOX6 (SPOTLIGHT) - 1L CLDN18,2-positif HER2-négatif gastrique/GEJ