Key result
In a patient with ifosfamide-induced encephalopathy, decreasing neuron-specific enolase levels from 20.41 to 7.69 µg/L correlated with EEG improvement and clinical recovery.
Why the study?
Ifosfamide can cause encephalopathy with variable clinical symptoms, but to date, no biomarkers have been evaluated for this condition.
Can Neuron-Specific Enolase (NSE) serve as a biomarker for clinical recovery in ifosfamide-induced encephalopathy?
Case Report (n=1)
Can Neuron-Specific Enolase (NSE) serve as a biomarker for clinical recovery in ifosfamide-induced encephalopathy?
Neuron-specific enolase (NSE) levels may correlate with clinical and EEG recovery in ifosfamide-induced encephalopathy, suggesting its potential utility as a biomarker.
Introduction: Ifosfamide, an alkylating agent, is used in treatment of various malignancies and may cause encephalopathies. The pathophysiology of this treatment adverse event is well documented, complex, and multifactorial, and involves the production of drug-related metabolites interfering with the normal functionality of neuronal synapses. Risk factors associated with the development of ifosfamide-induced encephalopathy have been identified including concurrent cisplatin administration and female gender. The clinical symptoms vary, ranging from simple confusion to seizure or coma. To date, no biomarkers have been evaluated in ifosfamide-induced encephalopathy. Neuron-specific enolase (NSE) elevation has already been correlated within toxic or metabolic encephalopathies regardless of the underlying etiology. Case Presentation: We report the case of a 56-year-old woman who received adjuvant chemotherapy for high-grade osteosarcoma including cisplatin, doxorubicin, and ifosfamide. The patient experienced ifosfamide-induced encephalopathy the day after completion of the ifosfamide infusion protocol. Treatment with methylene blue was initiated as soon as confusion developed. The patient presented behavioral problems, cognitive impairment, agitation, and aphasia, which resolved within few days, with persistent fatigue. NSE levels were assessed after every electroencephalogram (EEG). The kinetics of NSE levels from 20.41 to 7.69 µg/L and EEG toxic pattern improving from grade 2 to normal were consistent with recovery from clinical encephalopathy in this patient. Conclusion: Although increased levels of NSE in peripheral blood have been correlated with other etiologies of encephalopathy, its use as a companion biomarker for ifosfamide-induced encephalopathy warrants further investigation.
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Manchart et al. (2025) conducted a case report in Ifosfamide-induced encephalopathy (n=1). Neuron-specific enolase (NSE) monitoring was evaluated on Kinetics of NSE levels and EEG toxic pattern. In a patient with ifosfamide-induced encephalopathy, decreasing neuron-specific enolase levels from 20.41 to 7.69 µg/L correlated with EEG improvement and clinical recovery.
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