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Temozolomide

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDDRUG-TEMOZOLOMIDE
TypeDrug
Aliases
TemodalTemodarТемозоломід
Statusreviewed 2026-04-26 | pending_clinical_signoff
DiseasesDIS-GBM
SourcesSRC-EANO-GBM-2024 SRC-NCCN-CNS-2025

Drug Facts

ClassOral alkylating agent (imidazotetrazine)
MechanismMethylates DNA at O6/N7 of guanine. Crosses blood-brain barrier efficiently — backbone of Stupp protocol for newly-diagnosed glioblastoma (concurrent + adjuvant). MGMT promoter methylation predicts response (methylated → ~3× longer OS benefit vs unmethylated).
Typical dosingGBM Stupp concurrent: 75 mg/m² PO daily during RT (6 weeks). GBM Stupp adjuvant: 150-200 mg/m² PO days 1-5 of every 28-d cycle × 6 cycles (start at 150, escalate to 200 if tolerated).
Ukraine registeredTrue
NSZU reimbursedTrue
Ukraine last verified2026-04-27

Warnings

Notes

PJP prophylaxis (TMP-SMX 1 SS Mon/Wed/Fri or atovaquone 1500 mg daily, alternative dapsone 100 mg daily after G6PD screen) during concurrent RT + TMZ phase and adjuvant TMZ phase — universal lymphopenia (typically CD4 <200) creates opportunistic-infection risk window persisting weeks after the last cycle. MGMT promoter methylation testing is critical for treatment decision (Stupp NEJM 2005; Hegi NEJM 2005): methylated → ~3× greater OS benefit vs unmethylated. NOA-08 + Nordic trials: in elderly (>65) unmethylated → consider hypofractionated RT alone; methylated → TMZ-only or short-course RT + TMZ. CCNU + TMZ doublet (CeTeG/NOA-09) showed OS benefit in MGMT-methylated newly-dx GBM. Premedicate with 5-HT3 (ondansetron 8 mg) 1 hour before each dose; Mon-Fri schedules ease antiemetic burden. CBC weekly during concurrent RT, q2 weeks during adjuvant. UA: registered; НСЗУ-reimbursed for GBM (Stupp) + anaplastic glioma.

Used By

Regimens