Literature DB >> 26806759

Hematopoietic stem cell transplantation for inborn errors of metabolism: A report from the Research Committee on Transplantation for Inborn Errors of Metabolism of the Japanese Ministry of Health, Labour and Welfare and the Working Group of the Japan Society for Hematopoietic Cell Transplantation.

Shunichi Kato1, Hiromasa Yabe1, Hiromitsu Takakura1, Hideo Mugishima2, Mika Ishige2, Akemi Tanaka3, Koji Kato4, Nao Yoshida4, Souichi Adachi5, Norio Sakai6, Yoshiko Hashii6, Toya Ohashi7, Yoji Sasahara8, Yasuyuki Suzuki9, Ken Tabuchi10.   

Abstract

A total of 216 patients with IEM were treated by allogeneic HSCT in Japan from 1985 until 2010. The results of UCBT have improved, and the OS rate of UCBT (81.9%) was not different from those of RBMT (87.2%) or UBMT (73.9%) in 2000-2010. However, EFS rates in RBMT (73.2%) and UBMT (62.2%) were better than that in UCBT (49.5%), and the difference between RBMT and UCBT was significant (p = 0.01). The EFS rate of patients conditioned by RIC (74.6%) was comparable or slightly better than in those who underwent MAC with irradiation (57.9%) or without irradiation (54.2%) in 2000-2010. A more pronounced trend was observed toward differential EFS for UCBT in 2000-2010: RIC (62.9%), MAC with irradiation (20.0%), and MAC without irradiation (42.1%). The difference between RIC and MAC with irradiation was significant (p < 0.03). In summary, we report a Japanese registry analysis of HSCT for IEM with improving survival in UCBT. The introduction of RIC after 2000 was considered to contribute to this improvement. UCBT could be recommended for those who lack an HLA-identical sibling donor.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  hematopoietic stem cell transplantation; inborn errors of metabolism; national survey

Mesh:

Substances:

Year:  2016        PMID: 26806759     DOI: 10.1111/petr.12672

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  6 in total

1.  P-Tau and Subunit c Mitochondrial ATP Synthase Accumulation in the Central Nervous System of a Woman with Hurler-Scheie Syndrome Treated with Enzyme Replacement Therapy for 12 Years.

Authors:  Hiroshi Kobayashi; Masamichi Ariga; Yohei Sato; Masako Fujiwara; Nei Fukasawa; Takahiro Fukuda; Hiroyuki Takahashi; Masahiro Ikegami; Motomichi Kosuga; Torayuki Okuyama; Yoshikatsu Eto; Hiroyuki Ida
Journal:  JIMD Rep       Date:  2018-04-29

Review 2.  Allogeneic hematopoietic stem cell transplantation for inherited metabolic disorders.

Authors:  Hiromasa Yabe
Journal:  Int J Hematol       Date:  2022-05-20       Impact factor: 2.490

Review 3.  Unresolved issues in allogeneic hematopoietic cell transplantation for non-malignant diseases.

Authors:  Katsutsugu Umeda
Journal:  Int J Hematol       Date:  2022-05-14       Impact factor: 2.490

Review 4.  Transplantation as disease modifying therapy in adults with inherited metabolic disorders.

Authors:  Sandra Sirrs; Fady Hannah-Shmouni; Stephen Nantel; James Neuberger; Eric M Yoshida
Journal:  J Inherit Metab Dis       Date:  2018-02-01       Impact factor: 4.982

Review 5.  Recent trends in mucopolysaccharidosis research.

Authors:  Hiroshi Kobayashi
Journal:  J Hum Genet       Date:  2018-11-19       Impact factor: 3.172

6.  Potential Risks to Stable Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation for Children With Cerebral X-linked Adrenoleukodystrophy.

Authors:  Jörn-Sven Kühl; Jana Kupper; Hermann Baqué; Wolfram Ebell; Jutta Gärtner; Christoph Korenke; Birgit Spors; Ingo G Steffen; Gabriele Strauss; Sebastian Voigt; Bernhard Weschke; Almuth Weddige; Wolfgang Köhler; Robert Steinfeld
Journal:  JAMA Netw Open       Date:  2018-07-06
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.