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Liposomal irinotecan

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IDDRUG-LIPOSOMAL-IRINOTECAN
ТипПрепарат
Синоніми
MM-398OnivydePEP02nal-IRInanoliposomal irinotecanЛіпосомальний іринотекан
Статуспереглянуто 2026-05-08
ХворобиDIS-PDAC
ДжерелаSRC-ESMO-PANCREATIC-2024 SRC-NAPOLI-3-WAINBERG-2024 SRC-NCCN-PANCREATIC-2025

Дані про препарат

КласTopoisomerase I inhibitor (PEGylated liposomal nanoparticle formulation of irinotecan)
Механізм діїNanoliposomal (PEGylated) formulation of irinotecan that prolongs circulation time and enhances tumor accumulation via the enhanced permeability and retention (EPR) effect, increasing intra-tumoral conversion to active metabolite SN-38 (~100-1000× more potent than parent). SN-38 stabilizes the topoisomerase-I/DNA cleavable complex, producing single-strand DNA breaks that become lethal double-strand breaks during S-phase replication. SN-38 glucuronidation by UGT1A1 to inactive SN-38G is the main inactivation pathway; UGT1A1*28 homozygotes (Gilbert-syndrome variant) and *6 carriers have impaired clearance and increased risk of severe neutropenia and diarrhea — starting-dose reduction recommended. Compared with conventional irinotecan, the liposomal carrier delivers higher and more sustained intra-tumoral SN-38 exposure at lower peak plasma drug concentrations.
Типове дозуванняNALIRIFOX (1L mPDAC, NAPOLI-3): 50 mg/m² (free base, equivalent to ~60 mg/m² salt) IV over 90 min day 1 every 14 d, with oxaliplatin 60 mg/m² + leucovorin 400 mg/m² + 5-FU 2400 mg/m² CIV over 46 h. 2L mPDAC (NAPOLI-1, with 5-FU/LV): 70 mg/m² (free base, equivalent to ~80 mg/m² salt) IV over 90 min day 1 every 14 d. UGT1A1 *28/*28 or *6/*6: reduce starting dose ~25-30% (e.g. NAPOLI-1 schedule → 50 mg/m² free base; NALIRIFOX schedule → 40 mg/m² free base starting dose, escalate to 50 mg/m² if tolerated). Bilirubin >2× ULN: do not initiate — relieve biliary obstruction first.
Зареєстровано в УкраїніFalse
Відшкодовується НСЗУFalse
Остання перевірка для України2026-05-08

Застереження

Нотатки

ONIVYDE (liposomal irinotecan) is FDA-approved for two PDAC indications: (1) 1L mPDAC in combination with oxaliplatin + 5-FU + leucovorin (NALIRIFOX regimen) based on NAPOLI-3 (Wainberg, Lancet 2023; FDA approval 2024); (2) 2L mPDAC after gemcitabine-based 1L therapy in combination with 5-FU + leucovorin based on NAPOLI-1 (Wang-Gillam, Lancet 2016; FDA approval 2015). Dose is expressed in free-base equivalents per FDA label — the salt-equivalent conversion (free base × ~1.15) is found in older literature and may cause confusion; NAPOLI-3 used 50 mg/m² free base (NALIRIFOX), NAPOLI-1 used 70 mg/m² free base (2L). Liposomal formulation is NOT interchangeable with conventional irinotecan — different pharmacokinetics, different approved indications, distinct dosing. UGT1A1 testing strongly recommended before initiation; *28/*28 homozygotes need starting-dose reduction. Atropine 0.25-1 mg SC/IV for acute cholinergic syndrome (within 30 min of infusion). Loperamide schedule for late diarrhea: 4 mg at first loose stool then 2 mg q2h until 12 h diarrhea-free. ONIVYDE not registered in Ukraine — significant access barrier.

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