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Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future.
Taylor, Madeleine; Khan, Shaukat; Stapleton, Molly; Wang, Jianmin; Chen, Jing; Wynn, Robert; Yabe, Hiromasa; Chinen, Yasutsugu; Boelens, Jaap Jan; Mason, Robert W; Kubaski, Francyne; Horovitz, Dafne D G; Barth, Anneliese L; Serafini, Marta; Bernardo, Maria Ester; Kobayashi, Hironori; Orii, Kenji E; Suzuki, Yasuyuki; Orii, Tadao; Tomatsu, Shunji.
Afiliación
  • Taylor M; Department of Biomedical, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware; Deparment of Biological Science, University of Delaware, Newark, Delaware.
  • Khan S; Department of Biomedical, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware.
  • Stapleton M; Department of Biomedical, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware; Deparment of Biological Science, University of Delaware, Newark, Delaware.
  • Wang J; Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Chen J; Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Wynn R; Department of Paediatric Haematology and Cell Therapy, University of Manchester, Manchester, United Kingdom.
  • Yabe H; Department of Cell Transplantation and Regenerative Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Chinen Y; Department of Pediatrics, Faculty of Medicine, University of the Ryukyus, Nishihara, Japan.
  • Boelens JJ; Stem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Mason RW; Department of Biomedical, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware; Deparment of Biological Science, University of Delaware, Newark, Delaware.
  • Kubaski F; Medical Genetics Service, Hospital de ClÃnicas de Porto Alegre (HCPA), Department of Genetics and Molecular Biology- Program Partnership Graduate in Genetics and Molecular Biology (PPGBM), Federal University of Rio Grande do Sul (UFRGS), and National Institute of Populational Medical Genetics (INAGE
  • Horovitz DDG; Medical Genetics Department, National Institute of Women, Children, and Adolescent Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
  • Barth AL; Medical Genetics Department, National Institute of Women, Children, and Adolescent Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
  • Serafini M; Department of Pediatrics, Dulbecco Telethon Institute, University of Milano-Bicocca, Monza, Italy.
  • Bernardo ME; Pediatric Immunohematology and Bone Marrow Transplantation Unit, San Raffaele-Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Kobayashi H; Department of Pediatrics, Shimane University Faculty of Medicine, Shimane, Japan.
  • Orii KE; Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan.
  • Suzuki Y; Medical Education Development Center, Gifu University, Gifu, Japan.
  • Orii T; Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan.
  • Tomatsu S; Department of Biomedical, Nemours/Alfred I. duPont Hospital for Children, Wilmington, Delaware; Department of Pediatrics, Shimane University Faculty of Medicine, Shimane, Japan; Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan; Department of Pediatrics, Thomas Jeff
Biol Blood Marrow Transplant ; 25(7): e226-e246, 2019 07.
Article en En | MEDLINE | ID: mdl-30772512
ABSTRACT
Allogenic hematopoietic stem cell transplantation (HSCT) has proven to be a viable treatment option for a selected group of patients with mucopolysaccharidoses (MPS), including those with MPS types I, II, IVA, VI, and VII. Early diagnosis and timely referral to an expert in MPS are critical, followed by a complete examination and evaluation by a multidisciplinary team, including a transplantation physician. Treatment recommendations for MPS are based on multiple biological, sociological, and financial factors, including type of MPS, clinical severity, prognosis, present clinical signs and symptoms (disease stage), age at onset, rate of progression, family factors and expectations, financial burden, feasibility, availability, risks and benefits of available therapies such as HSCT, enzyme replacement therapy (ERT), surgical interventions, and other supportive care. International collaboration and data review are critical to evaluating the therapeutic efficacy and adverse effects of HSCT for MPS. Collaborative efforts to assess HSCT for MPS have been ongoing since the first attempt at HSCT in a patient with MPS reported in 1981. The accumulation of data since then has made it possible to identify early outcomes (ie, transplantation outcomes) and long-term disease-specific outcomes resulting from HSCT. The recent identification of predictive factors and the development of innovative regimens have significantly improved the outcomes of both engraftment failure and transplantation-related mortality. Assessment of long-term outcomes has considered a variety of factors, including type of MPS, type of graft, age at transplantation, and stage of disease progression, among others. Studies on long-term outcomes are considered a key factor in the use of HSCT in patients with MPS. These studies have shown the effects and limitations of HSCT on improving disease manifestations and quality of life. In this review, we summarize the efficacy, side effects, risks, and cost of HSCT for each type of MPS.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mucopolisacaridosis / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Guideline / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Biol Blood Marrow Transplant Asunto de la revista: HEMATOLOGIA / TRANSPLANTE Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mucopolisacaridosis / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Guideline / Prognostic_studies / Screening_studies Límite: Humans Idioma: En Revista: Biol Blood Marrow Transplant Asunto de la revista: HEMATOLOGIA / TRANSPLANTE Año: 2019 Tipo del documento: Article