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Acute neurotoxicity after intrathecal cytosine arabinoside in two adolescents with acute lymphoblastic leukemia of B‐cell type
Author(s) -
Resar Linda M. S.,
Phillips Peter C.,
Kastan Michael B.,
Leventhal Brigid G.,
Bowman Paul W.,
Civin Curt I.
Publication year - 1993
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19930101)71:1<117::aid-cncr2820710119>3.0.co;2-k
Subject(s) - medicine , neurotoxicity , cytarabine , discontinuation , encephalopathy , methotrexate , acute lymphocytic leukemia , myelopathy , leukemia , anesthesia , gastroenterology , toxicity , spinal cord , lymphoblastic leukemia , psychiatry
Background . Two adolescents with acute B‐cell leukemia (Burkitt leukemia) had acute severe neurotoxicity after treatment with intrathecal (IT) cytosine arabinoside (AraC) at a dose of 50 mg/day for three consecutive days. Results . A 16‐year‐old boy had a rapidly ascending myelopathy and encephalopathy 20 hours after receiving the third dose of IT AraC. He remained quadriplegic and required ventilatory assistance for 10 months until his death from progressive tumor. A 12‐year‐old girl had acute encephalopathy, seizures, and focal neuroimaging abnormalities in the cerebellum and brain stem within 32 hours of the third AraC dose and 8 hours after IT methotrexate (MTX, 12 mg). Her clinical neurologic deficits resolved during the ensuing month. Patient 1 represents the first report to the authors' knowledge of acute severe neurotoxicity after AraC administered as the only IT drug. In Patient 2, IT AraC neurotoxicity may have been potentiated by the single dose of MTX. Conclusion . IT AraC administered for 3 or more consecutive days may lead to profound neurologic dysfunction and require discontinuation of therapy. Cancer 1993; 71:117‐23.