TY - JOUR
T1 - Dorsal column myelopathy after intrathecal chemotherapy for leukemia
AU - Pinnix, Chelsea C.
AU - Chi, Linda
AU - Jabbour, Elias J.
AU - Milgrom, Sarah A.
AU - Smith, Grace L.
AU - Daver, Naval
AU - Garg, Naveen
AU - Cykowski, Matthew D.
AU - Fuller, Greg
AU - Cachia, David
AU - Kamiya-Matsuoka, Carlos
AU - Woodman, Karin
AU - Dinardo, Courtney
AU - Jain, Nitin
AU - Kadia, Tapan M.
AU - Pemmaraju, Naveen
AU - Ohanian, Maro
AU - Konopleva, Marina
AU - Kantarjian, Hagop M.
AU - Dabaja, Bouthaina S.
N1 - Publisher Copyright:
© 2016 Wiley Periodicals, Inc.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Intrathecal chemotherapy with methotrexate, a folate antagonist, is widely used to treat central nervous system malignancies. The mechanisms underlying methotrexate-induced neurotoxicity are unclear but may be related to increased homocysteine levels. Intrathecal methotrexate-induced myelopathy mimicking subacute combined degeneration, with normal B12 levels, has been documented. We examined treatment and magnetic resonance imaging (MRI) characteristics of 13 patients with leukemia who received intrathecal methotrexate and developed urinary and bowel incontinence, ascending motor weakness, and sensory loss with dorsal column hyperintensity on MRI between 2000 and 2016. Cerebrospinal fluid evaluation was negative for leukemia in all patients and positive for elevated protein in 12 patients. Seven of eight patients with available data had reduced serum folate, increased serum homocysteine, or both, implicating methotrexate as the cause of neurotoxicity. Autopsy of one patient revealed loss of myelinated axons in the posterior columns. These findings suggest that methotrexate neurotoxicity may be mediated by folate antagonism. Awareness and a high index of suspicion of these characteristic clinical and radiographic features in patients who develop myelopathy after intrathecal methotrexate may help to avoid additional neurotoxic therapy in such patients.
AB - Intrathecal chemotherapy with methotrexate, a folate antagonist, is widely used to treat central nervous system malignancies. The mechanisms underlying methotrexate-induced neurotoxicity are unclear but may be related to increased homocysteine levels. Intrathecal methotrexate-induced myelopathy mimicking subacute combined degeneration, with normal B12 levels, has been documented. We examined treatment and magnetic resonance imaging (MRI) characteristics of 13 patients with leukemia who received intrathecal methotrexate and developed urinary and bowel incontinence, ascending motor weakness, and sensory loss with dorsal column hyperintensity on MRI between 2000 and 2016. Cerebrospinal fluid evaluation was negative for leukemia in all patients and positive for elevated protein in 12 patients. Seven of eight patients with available data had reduced serum folate, increased serum homocysteine, or both, implicating methotrexate as the cause of neurotoxicity. Autopsy of one patient revealed loss of myelinated axons in the posterior columns. These findings suggest that methotrexate neurotoxicity may be mediated by folate antagonism. Awareness and a high index of suspicion of these characteristic clinical and radiographic features in patients who develop myelopathy after intrathecal methotrexate may help to avoid additional neurotoxic therapy in such patients.
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U2 - 10.1002/ajh.24611
DO - 10.1002/ajh.24611
M3 - Article
C2 - 27874212
AN - SCOPUS:85009792087
SN - 0361-8609
VL - 92
SP - 155
EP - 160
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 2
ER -