| Literature DB >> 28673849 |
Francyne Kubaski1, Hiromasa Yabe2, Yasuyuki Suzuki3, Toshiyuki Seto4, Takashi Hamazaki4, Robert W Mason5, Li Xie6, Tor Gunnar Hugo Onsten7, Sandra Leistner-Segal8, Roberto Giugliani9, Vũ Chí Dũng10, Can Thi Bich Ngoc10, Seiji Yamaguchi11, Adriana M Montaño12, Kenji E Orii13, Toshiyuki Fukao13, Haruo Shintaku4, Tadao Orii13, Shunji Tomatsu14.
Abstract
There is limited information regarding the long-term outcomes of hematopoietic stem cell transplantation (HSCT) for mucopolysaccharidosis II (MPS II). In this study, clinical, biochemical, and radiologic findings were assessed in patients who underwent HSCT and/or enzyme replacement therapy (ERT). Demographic data for 146 HSCT patients were collected from 27 new cases and 119 published cases and were compared with 51 ERT and 15 untreated cases. Glycosaminoglycan (GAG) levels were analyzed by liquid chromatography tandem mass spectrometry in blood samples from HSCT, ERT, and untreated patients as well as age-matched controls. Long-term magnetic resonance imaging (MRI) findings were investigated in 13 treated patients (6 ERT and 7 HSCT). Mean age at HSCT was 5.5 years (range, 2 to 21.4 years) in new patients and 5.5 years (range, 10 months to 19.8 years) in published cases. None of the 27 new patients died as a direct result of the HSCT procedure. Graft-versus-host disease occurred in 8 (9%) out of 85 published cases, and 9 (8%) patients died from transplantation-associated complications. Most HSCT patients showed greater improvement in somatic features, joint movements, and activity of daily living than the ERT patients. GAG levels in blood were significantly reduced by ERT and levels were even lower after HSCT. HSCT patients showed either improvement or no progression of abnormal findings in brain MRI while abnormal findings became more extensive after ERT. HSCT seems to be more effective than ERT for MPS II in a wide range of disease manifestations and could be considered as a treatment option for this condition.Entities:
Keywords: Enzyme replacement therapy; Hematopoietic stem cell transplantation; Hunter syndrome; Iduronate-2-sulfatase; Mucopolysaccharidosis II
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Year: 2017 PMID: 28673849 PMCID: PMC5659208 DOI: 10.1016/j.bbmt.2017.06.020
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742