TY - JOUR
T1 - Allogeneic stem cell transplantation with reduced intensity conditioning for patients with adrenoleukodystrophy
AU - Kato, Koji
AU - Maemura, Ryo
AU - Wakamatsu, Manabu
AU - Yamamori, Ayako
AU - Hamada, Motoharu
AU - Kataoka, Shinsuke
AU - Narita, Atsushi
AU - Miwata, Shunsuke
AU - Sekiya, Yuko
AU - Kawashima, Nozomu
AU - Suzuki, Kyogo
AU - Narita, Kotaro
AU - Doisaki, Sayoko
AU - Muramatsu, Hideki
AU - Sakaguchi, Hirotoshi
AU - Matsumoto, Kimikazu
AU - Koike, Yuka
AU - Onodera, Osamu
AU - Kaga, Makiko
AU - Shimozawa, Nobuyuki
AU - Yoshida, Nao
N1 - Publisher Copyright:
© 2018 The Authors
PY - 2019/3
Y1 - 2019/3
N2 - Objective: The prognosis of adrenoleukodystrophy (ALD)with neurological involvement is generally dismal; however, allogeneic stem cell transplantation (SCT) is recognized as effective to stabilize or improve the clinical symptoms of ALD. Herein, we report the clinical outcomes of patients with ALD who consecutively underwent allogeneic stem cell transplantation with reduced intensity conditioning at our institution. Patients: Sixteen patients with ALD, who were symptomatic (n = 14) or presymptomatic (n = 2), received SCT from 2010 to 2016. The stem cell source was cord blood (n = 14), or bone marrow from a human leukocyte antigen identical sibling (n = 2). The conditioning regimen prior to transplantation was reduced intensity and consisted of fludarabine (125 mg/m2), melphalan (140 mg/m2) and low dose total body irradiation (TBI) of 4Gy (n = 15) or 3Gy (n = 1). Results: Primary engraftment was obtained in 11 patients, and 4 of the 5 patients who lost the primary graft received a second cord blood transplantation and were engrafted. Five years overall and event-free survival were 90.9% and 61.1% respectively, with a median of 45 months (range 16–91). Loes score stabilized or improved by 18 months after transplantation except for patients with internal capsule involvement. Conclusion: Allogeneic SCT with reduced intensity conditioning for patients with ALD was safely performed without major transplant-related complications even in symptomatic patients and neurological symptoms were stabilized after SCT in patients without internal capsule involvement.
AB - Objective: The prognosis of adrenoleukodystrophy (ALD)with neurological involvement is generally dismal; however, allogeneic stem cell transplantation (SCT) is recognized as effective to stabilize or improve the clinical symptoms of ALD. Herein, we report the clinical outcomes of patients with ALD who consecutively underwent allogeneic stem cell transplantation with reduced intensity conditioning at our institution. Patients: Sixteen patients with ALD, who were symptomatic (n = 14) or presymptomatic (n = 2), received SCT from 2010 to 2016. The stem cell source was cord blood (n = 14), or bone marrow from a human leukocyte antigen identical sibling (n = 2). The conditioning regimen prior to transplantation was reduced intensity and consisted of fludarabine (125 mg/m2), melphalan (140 mg/m2) and low dose total body irradiation (TBI) of 4Gy (n = 15) or 3Gy (n = 1). Results: Primary engraftment was obtained in 11 patients, and 4 of the 5 patients who lost the primary graft received a second cord blood transplantation and were engrafted. Five years overall and event-free survival were 90.9% and 61.1% respectively, with a median of 45 months (range 16–91). Loes score stabilized or improved by 18 months after transplantation except for patients with internal capsule involvement. Conclusion: Allogeneic SCT with reduced intensity conditioning for patients with ALD was safely performed without major transplant-related complications even in symptomatic patients and neurological symptoms were stabilized after SCT in patients without internal capsule involvement.
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U2 - 10.1016/j.ymgmr.2018.11.001
DO - 10.1016/j.ymgmr.2018.11.001
M3 - Article
AN - SCOPUS:85056756721
SN - 2214-4269
VL - 18
SP - 1
EP - 6
JO - Molecular Genetics and Metabolism Reports
JF - Molecular Genetics and Metabolism Reports
ER -