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Pralatrexate

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

IDDRUG-PRALATREXATE
TypeDrug
Aliases
FolotynПралатрексат
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-PTCL-NOS
SourcesSRC-NCCN-BCELL-2025

Drug Facts

ClassAntifolate (selective for RFC-1 transporter — accumulates in malignant T-cells)
MechanismFolate analog with high affinity for reduced folate carrier-1 (RFC-1) transporter, selectively accumulating in malignant T-cells and inhibiting dihydrofolate reductase (DHFR). Internal polyglutamation traps the drug intracellularly. Mechanism distinct from methotrexate — designed for selective uptake in T-cell malignancies.
Typical dosing30 mg/m² IV push over 3-5 min, weekly × 6 of every 7-week cycle, until progression or unacceptable toxicity
Ukraine registeredFalse
NSZU reimbursedFalse
Ukraine last verified2026-04-27

Warnings

Notes

PROPEL trial (O'Connor 2011): r/r PTCL n=111 (incl PTCL NOS, AITL, ALCL ALK-, transformed MF) — ORR 29%, CR 11%, mDOR 10.1 mo. FDA- approved for r/r PTCL after ≥1 prior line. Mucositis is dominant dose-limiting toxicity — MANDATORY folate 1 mg PO daily + vitamin B12 1 mg IM every 8-10 weeks throughout therapy + oral cryotherapy / cold-water gargle during infusion to mitigate. Major UA access barrier: not registered + not EMA-approved.

Used By

Regimens