Literature DB >> 28054207

Mortality after hematopoietic stem cell transplantation for severe mucopolysaccharidosis type I: the 30-year University of Minnesota experience.

Nathan J Rodgers1, Alexander M Kaizer2, Weston P Miller3, Kyle D Rudser2, Paul J Orchard3, Elizabeth A Braunlin4.   

Abstract

BACKGROUND AND AIM: Mucopolysaccharidosis IH (MPS IH, Hurler syndrome) naturally leads to death within the first decade of life, primarily from cardiac and pulmonary causes. To determine how hematopoietic stem cell transplantation (HSCT) has altered mortality, we analyzed our institution's 30-year experience of patients with MPS IH undergoing HSCT.
METHODS: Using chart review and the National Death Index, we determined survival status of 134 patients (males = 69) with MPS IH transplanted between 9/16/1983 and 7/25/2013 on 12/31/2013. Analysis included descriptive statistics, Kaplan-Meier curves, and regression analysis by Cox proportional hazards model.
RESULTS: Overall survival (95% CI) at one- and 25-years was 70% (62-78%) and 37% (19-55%), respectively. From 2004 onward, overall survival at one- and 8-years was 84% (73-96%) and 81% (69-94%), respectively, compared to 65% (55-74%) and 57% (47-67%) prior to 2004 (Log-rank p = 0.032). Regardless of era, male survival was significantly better than female (HR 0.40, [95% CI: 0.21-0.74], p = 0.004). The cumulative incidence of death (95% CI) at 25 years was 63% (45-81%); incidence of pulmonary-related death was the highest at 27% (10-41%) compared to 8% (0.3-16%) for cardiac, 12% (6-17%) for infectious disease, and 16% (3-27%) from other complications.
CONCLUSIONS: HSCT has increased survival in MPS IH beyond the third decade of life and decreased the incidence of cardiac mortality, but deaths after the third year post-HSCT occur in excess of expected US mortality. It is important to determine if improved transplant strategies since 2004 result in better long-term survival in the current patient population.

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Year:  2017        PMID: 28054207     DOI: 10.1007/s10545-016-0006-2

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  24 in total

1.  Pre-transplant risk factors affecting outcome in Hurler syndrome.

Authors:  P J Orchard; C Milla; E Braunlin; T DeFor; K Bjoraker; B R Blazar; C Peters; J Wagner; J Tolar
Journal:  Bone Marrow Transplant       Date:  2009-11-09       Impact factor: 5.483

2.  Outcomes of haematopoietic stem cell transplantation for inherited metabolic disorders: a report from the Australian and New Zealand Children's Haematology Oncology Group and the Australasian Bone Marrow Transplant Recipient Registry.

Authors:  R Mitchell; I Nivison-Smith; A Anazodo; K Tiedemann; P J Shaw; L Teague; C J Fraser; T L Carter; H Tapp; F Alvaro; T A O'Brien
Journal:  Pediatr Transplant       Date:  2013-06-27

3.  Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study.

Authors:  Mieke Aldenhoven; Robert F Wynn; Paul J Orchard; Anne O'Meara; Paul Veys; Alain Fischer; Vassili Valayannopoulos; Benedicte Neven; Attilio Rovelli; Vinod K Prasad; Jakub Tolar; Heather Allewelt; Simon A Jones; Rossella Parini; Marleen Renard; Victoria Bordon; Nico M Wulffraat; Tom J de Koning; Elsa G Shapiro; Joanne Kurtzberg; Jaap Jan Boelens
Journal:  Blood       Date:  2015-01-26       Impact factor: 22.113

4.  Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome.

Authors:  J Cox-Brinkman; J-J Boelens; J E Wraith; A O'meara; P Veys; F A Wijburg; N Wulffraat; R F Wynn
Journal:  Bone Marrow Transplant       Date:  2006-05-22       Impact factor: 5.483

5.  Non-TBI hematopoietic stem cell transplantation in pediatric AML patients: a single-center experience.

Authors:  Amir A Hamidieh; Kamran Alimoghaddam; Mohammad Jahani; Babak Bahar; Seyed Asadollah Mousavi; Masood Iravani; Maryam Behfar; Arash Jalali; Mahdi Jalili; Amir Hamdi; Ardeshir Ghavamzadeh
Journal:  J Pediatr Hematol Oncol       Date:  2013-08       Impact factor: 1.289

6.  Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources.

Authors:  G Souillet; N Guffon; I Maire; M Pujol; P Taylor; F Sevin; N Bleyzac; C Mulier; A Durin; K Kebaili; C Galambrun; Y Bertrand; R Froissart; C Dorche; L Gebuhrer; C Garin; J Berard; P Guibaud
Journal:  Bone Marrow Transplant       Date:  2003-06       Impact factor: 5.483

7.  Follow-up of nine patients with Hurler syndrome after bone marrow transplantation.

Authors:  N Guffon; G Souillet; I Maire; J Straczek; P Guibaud
Journal:  J Pediatr       Date:  1998-07       Impact factor: 4.406

8.  The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK.

Authors:  David Moore; Martin J Connock; Ed Wraith; Christine Lavery
Journal:  Orphanet J Rare Dis       Date:  2008-09-16       Impact factor: 4.123

Review 9.  Microglia: the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases.

Authors:  W Krivit; J H Sung; E G Shapiro; L A Lockman
Journal:  Cell Transplant       Date:  1995 Jul-Aug       Impact factor: 4.139

10.  Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure.

Authors:  J J Boelens; R F Wynn; A O'Meara; P Veys; Y Bertrand; G Souillet; J E Wraith; A Fischer; M Cavazzana-Calvo; K W Sykora; P Sedlacek; A Rovelli; C S P M Uiterwaal; N Wulffraat
Journal:  Bone Marrow Transplant       Date:  2007-05-28       Impact factor: 5.483

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  10 in total

1.  Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutations.

Authors:  Mehdi Shafaat; Mehrdad Hashemi; Ahmad Majd; Maryam Abiri; Sirous Zeinali
Journal:  Metab Brain Dis       Date:  2019-06-24       Impact factor: 3.584

Review 2.  Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future.

Authors:  Madeleine Taylor; Shaukat Khan; Molly Stapleton; Jianmin Wang; Jing Chen; Robert Wynn; Hiromasa Yabe; Yasutsugu Chinen; Jaap Jan Boelens; Robert W Mason; Francyne Kubaski; Dafne D G Horovitz; Anneliese L Barth; Marta Serafini; Maria Ester Bernardo; Hironori Kobayashi; Kenji E Orii; Yasuyuki Suzuki; Tadao Orii; Shunji Tomatsu
Journal:  Biol Blood Marrow Transplant       Date:  2019-02-14       Impact factor: 5.742

Review 3.  Allogeneic hematopoietic stem cell transplantation for inherited metabolic disorders.

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

4.  The Outcome of Allogeneic Hematopoietic Stem Cell Transplantation From Different Donors in Recipients With Mucopolysaccharidosis.

Authors:  Yuhua Qu; Hao Liu; Likun Wei; Shushan Nie; Wenjiao Ding; Sha Liu; Haiyan Liu; Hua Jiang
Journal:  Front Pediatr       Date:  2022-06-30       Impact factor: 3.569

5.  Contribution of the innate and adaptive immune systems to aortic dilation in murine mucopolysaccharidosis type I.

Authors:  Elizabeth Braunlin; Juan E Abrahante; Ron McElmurry; Michael Evans; Miles Smith; Davis Seelig; M Gerard O'Sullivan; Jakub Tolar; Chester B Whitley; R Scott McIvor
Journal:  Mol Genet Metab       Date:  2022-02-03       Impact factor: 4.204

Review 6.  Therapeutic Options for Mucopolysaccharidoses: Current and Emerging Treatments.

Authors:  Kazuki Sawamoto; Molly Stapleton; Carlos J Alméciga-Díaz; Angela J Espejo-Mojica; Juan Camilo Losada; Diego A Suarez; Shunji Tomatsu
Journal:  Drugs       Date:  2019-07       Impact factor: 11.431

7.  Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism.

Authors:  Jean T Pantel; Max Zhao; Martin A Mensah; Nurulhuda Hajjir; Tzung-Chien Hsieh; Yair Hanani; Nicole Fleischer; Tom Kamphans; Stefan Mundlos; Yaron Gurovich; Peter M Krawitz
Journal:  J Inherit Metab Dis       Date:  2018-04-05       Impact factor: 4.982

Review 8.  Mucopolysaccharidoses I and II: Brief Review of Therapeutic Options and Supportive/Palliative Therapies.

Authors:  Haiyan Nan; Chanbum Park; Sungho Maeng
Journal:  Biomed Res Int       Date:  2020-12-04       Impact factor: 3.411

Review 9.  Mucopolysaccharidosis Type I: Current Treatments, Limitations, and Prospects for Improvement.

Authors:  Christiane S Hampe; Jacob Wesley; Troy C Lund; Paul J Orchard; Lynda E Polgreen; Julie B Eisengart; Linda K McLoon; Sebahattin Cureoglu; Patricia Schachern; R Scott McIvor
Journal:  Biomolecules       Date:  2021-01-29

Review 10.  MPSI Manifestations and Treatment Outcome: Skeletal Focus.

Authors:  Giada De Ponti; Samantha Donsante; Marta Frigeni; Alice Pievani; Alessandro Corsi; Maria Ester Bernardo; Mara Riminucci; Marta Serafini
Journal:  Int J Mol Sci       Date:  2022-09-22       Impact factor: 6.208

  10 in total

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