TY - JOUR
T1 - Nelarabine-induced myelopathy in patients undergoing allogeneic hematopoietic cell transplantation
T2 - a report of three cases
AU - Fukuta, Takanori
AU - Tanaka, Takashi
AU - Hashimoto, Taiki
AU - Isahaya, Kenji
AU - Kubo, Yuko
AU - Yamano, Yoshihisa
AU - Satomi, Kaishi
AU - Hiraoka, Nobuyoshi
AU - Shirakawa, Nami
AU - Arakawa, Ayumu
AU - Ogawa, Chitose
AU - Nishimura, Nao
AU - Aoki, Jun
AU - Ito, Ayumu
AU - Inamoto, Yoshihiro
AU - Kim, Sung Won
AU - Fukuda, Takahiro
N1 - Publisher Copyright:
© 2023, Japanese Society of Hematology.
PY - 2023/6
Y1 - 2023/6
N2 - Nelarabine is an effective treatment for T-cell acute lymphoblastic leukemia/lymphoma. Myelopathy is a rare but serious adverse event associated with this drug. Three patients who received nelarabine at the National Cancer Center Hospital from December 2014 to March 2021 developed myelopathy 20 days before, 12 days after, and 29 days after allogeneic hematopoietic cell transplantation (allo-HCT), respectively. Magnetic resonance imaging showed that two of the patients had lesions in the dorsal column or medulla oblongata, and one had no abnormalities in the head or spine. Despite treatment with intravenous immunoglobulin and methylprednisolone, all patients became unable to walk. One patient died on day 101 after allo-HCT due to progressive neurotoxicity. The other two patients showed spontaneous improvement in neurological symptoms, but one died of mucormycosis on day 476. Autopsy revealed spongiosis in the posterior funiculus in both patients who died, and also in the medulla oblongata in one patient. In the surviving patient, positron emission tomography on day 84 showed abnormal accumulation, suggesting continued inflammation. These cases demonstrated pathophysiological features of nelarabine-induced myelopathy and indicate that allo-HCT may worsen the condition. It is necessary to elucidate the underlying mechanism and establish diagnostic methods and therapies.
AB - Nelarabine is an effective treatment for T-cell acute lymphoblastic leukemia/lymphoma. Myelopathy is a rare but serious adverse event associated with this drug. Three patients who received nelarabine at the National Cancer Center Hospital from December 2014 to March 2021 developed myelopathy 20 days before, 12 days after, and 29 days after allogeneic hematopoietic cell transplantation (allo-HCT), respectively. Magnetic resonance imaging showed that two of the patients had lesions in the dorsal column or medulla oblongata, and one had no abnormalities in the head or spine. Despite treatment with intravenous immunoglobulin and methylprednisolone, all patients became unable to walk. One patient died on day 101 after allo-HCT due to progressive neurotoxicity. The other two patients showed spontaneous improvement in neurological symptoms, but one died of mucormycosis on day 476. Autopsy revealed spongiosis in the posterior funiculus in both patients who died, and also in the medulla oblongata in one patient. In the surviving patient, positron emission tomography on day 84 showed abnormal accumulation, suggesting continued inflammation. These cases demonstrated pathophysiological features of nelarabine-induced myelopathy and indicate that allo-HCT may worsen the condition. It is necessary to elucidate the underlying mechanism and establish diagnostic methods and therapies.
KW - Allogeneic hematopoietic cell transplantation
KW - Autopsy
KW - Myelopathy
KW - Nelarabine
KW - T-cell acute lymphoblastic leukemia/lymphoma
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U2 - 10.1007/s12185-023-03539-5
DO - 10.1007/s12185-023-03539-5
M3 - Article
C2 - 36705847
AN - SCOPUS:85146922225
SN - 0925-5710
VL - 117
SP - 933
EP - 940
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 6
ER -