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Neurotoxicity and Elevated Cerebrospinal-Fluid Methotrexate Concentration in Meningeal Leukemia
334
Citations
8
References
1973
Year
NeurotoxicologyApparent Antifolate Half-lifePharmacotherapyAdverse Drug ReactionHematological MalignancyClinical InjuryCerebrospinal FluidHematologyDrug MonitoringToxicologyNeurologyBrain InjuryNeuropathologyNeuroimmunologyClinical ToxicologyHealth SciencesTherapeutic Drug MonitoringNeurological MonitoringNeuropharmacologyNeuroprotectionPharmacologyNeurological AssessmentAntifolate ValuesForensic ToxicologyCentral Nervous SystemMeningeal LeukemiaMedicinePharmacokinetics
Cerebrospinal‑fluid methotrexate levels were measured in 25 patients receiving intrathecal therapy for meningeal leukemia. Patients with severe neurotoxicity had cerebrospinal‑fluid methotrexate concentrations 13.8 times higher than asymptomatic patients, and extreme elevations (20–100×) were associated with fatal myelopathy or irreversible neurologic sequelae, indicating that neurotoxicity likely results from prolonged exposure to excessive drug concentrations. Published in N Engl J Med 289:770–773, 1973.
Cerebrospinal-fluid methotrexate concentration was measured in 25 patients receiving intrathecal therapy for prophylaxis or treatment of meningeal leukemia. In 20 patients with no manifestations of neurotoxicity, the mean antifolate value in the cerebrospinal fluid was 1.7 X 10–7 M two days after administration of 12 to 15 mg per square meter of intrathecal methotrexate, and declined thereafter with a half-life of 12 to 18 hours. Five patients with severe neurotoxicity had cerebrospinal-fluid methotrexate concentrations averaging 13.8 times higher than the mean, and these concentrations were consistently higher than the range of antifolate values in the asymptomatic patients. One patient with values 20 to 100 times greater than the mean in asymptomatic patients sustained a fatal myelopathy, and in another, with an apparent antifolate half-life of 48 hours, irreversible neurologic sequelae developed. These observations suggest that the neurotoxicity associated with intrathecal methotrexate may be secondary to prolonged exposure to excessive drug concentrations in the central nervous system. (N Engl J Med 289:770–773, 1973)
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