Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioning

被引:150
|
作者
Boelens, Jaap Jan [1 ]
Aldenhoven, Mieke [1 ]
Purtill, Duncan [2 ]
Ruggeri, Annalisa [2 ]
DeFor, Todd [3 ]
Wynn, Robert [4 ]
Wraith, Ed [5 ]
Cavazzana-Calvo, Marina [6 ,7 ]
Rovelli, Attilio [8 ]
Fischer, Alain [6 ]
Tolar, Jakub [3 ]
Prasad, Vinod K. [9 ]
Escolar, Maria [10 ]
Gluckman, Eliane [2 ]
O'Meara, Anne [11 ]
Orchard, Paul J. [3 ]
Veys, Paul [12 ]
Eapen, Mary [13 ]
Kurtzberg, Joanne [9 ]
Rocha, Vanderson [2 ,14 ]
机构
[1] Univ Med Ctr Utrecht, Pediat Blood & Marrow Transplantat Program, NL-3584 EA Utrecht, Netherlands
[2] Eurocord Hop St Louis, Dept Hematol BMT, Paris, France
[3] Univ Minnesota, Program Blood & Marrow Transplantat, Minneapolis, MN USA
[4] Royal Manchester Childrens Hosp, Dept Hematol BMT, Manchester M27 1HA, Lancs, England
[5] St Marys Hosp, Manchester Acad Hlth Sci Ctr Genet Med, Manchester M13 0JH, Lancs, England
[6] Hop Univ Necker Enfants Malad, AP HP, Dept Biotherapie, Paris, France
[7] Univ Paris 05, Sorbonne Paris Cite, IMAGINE Inst, Paris, France
[8] Univ Milano Bicocca, Pediat Clin, Ctr Trapianto Midollo Osseo Fdn MBBM, Monza, Italy
[9] Duke Univ, Div Pediat Blood & Marrow Transplantat, Durham, NC USA
[10] Univ Pittsburgh, Program Study Neurodev Rare Disorders, Pittsburgh, PA USA
[11] Our Ladys Childrens Hosp, Dept Hematol & BMT, Dublin, Ireland
[12] Great Ormond St Hosp Sick Children, Blood & Marrow Transplantat Program, London, England
[13] Med Coll Wisconsin, Dept Med, Ctr Int Blood & Marrow Transplant Res, Milwaukee, WI 53226 USA
[14] Oxford Univ Hosp, Oxford, England
关键词
CORD BLOOD TRANSPLANTATION; ENZYME-REPLACEMENT THERAPY; RISK-FACTOR ANALYSIS; BONE-MARROW; PEDIATRIC-PATIENTS; GRAFT; DISEASE; COMBINATION;
D O I
10.1182/blood-2012-09-455238
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report transplantation outcomes of 258 children with Hurler syndrome (HS) after a myeloablative conditioning regimen from 1995 to 2007. Median age at transplant was 16.7 months and median follow-up was 57 months. The cumulative incidence of neutrophil recovery at day 60 was 91%, acute graft-versus-host disease (GVHD) (grade II-IV) at day 100 was 25%, and chronic GVHD and 5 years was 16%. Overall survival and event-free survival (EFS) at 5 years were 74% and 63%, respectively. EFS after HLA-matched sibling donor (MSD) and 6/6 matched unrelated cord blood (CB) donor were similar at 81%, 66% after 10/10 HLA-matched unrelated donor (UD), and 68% after 5/6 matched CB donor. EFS was lower after transplantation in 4/6 matched unrelated CB (UCB) (57%; P = .031) and HLA-mismatched UD (41%; P = .007). Full-donor chimerism (P = .039) and normal enzyme levels (P = .007) were higher after CB transplantation (92% and 98%, respectively) compared with the other grafts sources (69% and 59%, respectively). In conclusion, results of allogeneic transplantation for HS are encouraging, with similar EFS rates after MSD, 6/6 matched UCB, 5/6 UCB, and 10/10 matched UD. The use of mismatched UD and 4/6 matched UCB was associated with lower EFS.
引用
收藏
页码:3981 / 3987
页数:7
相关论文
共 50 条
  • [21] Antiphospholipid syndrome after non-myeloablative hematopoietic cell transplantation
    Mata, R.
    Llamas, R.
    Roman, A.
    Prieto, E.
    Lopez, J. L.
    Tomas, J. F.
    Subira, D.
    THROMBOSIS RESEARCH, 2008, 122 (02) : 283 - 284
  • [22] Ocular Outcomes of Combination Enzyme Replacement Therapy with Hematopoietic Cell Transplantation in Hurler Syndrome
    Decanini, Alejandra
    Tokarev, Julian
    Eisengart, Julie
    Shapiro, Elsa
    Summers, C. Gail
    Orchard, Paul
    Tolar, Jakub
    Bothun, Erick D.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [23] Haematopoietic cell transplantation for children with Hurler syndrome
    Diaz de Heredia, C.
    Olive, T.
    Ortega, J.
    Vizmanos, D.
    Sanchez de Toledo, J.
    BONE MARROW TRANSPLANTATION, 2007, 39 : S86 - S86
  • [24] Allogeneic hematopoietic cell transplantation (HCT) with nonmyeloablative conditioning after failed myeloablative HCT: Factors affecting outcomes.
    Baron, F
    Storb, R
    Storer, B
    Maloney, D
    Maris, M
    Niederwieser, D
    Shizuru, J
    Chauncey, T
    Bruno, B
    Forman, S
    McSweeney, P
    Maziarz, R
    Pulsipher, M
    Agura, E
    Sorror, M
    Wade, J
    Sandmaier, B
    BLOOD, 2005, 106 (11) : 333A - 333A
  • [25] ALLOGENEIC UNRELATED HEMATOPOIETIC STEM CELL TRANSPLANTATION WITH REDUCED INTENSITY CONDITIONING (RIC) IN CHILDREN WITH HURLER SYNDROME (SINGLE CENTRE EXPERIENCE)
    Borovkova, A. Svyatoslavovna
    Stancheva, N. Vasilievna
    Ratc, A. Alekseevna
    Kozhokar, P. Valerievna
    Razumova, S. Victorovna
    Bykova, T. Alexandrovna
    Semenova, E. Vladimirovna
    Paina, O. Vladimirovna
    Marcova, I. Victorovna
    Smirennikova, M. Mihaylovna
    Ekushov, K. Alexandrovich
    Fedukova, Y. Gennadievna
    Zubarovskaya, L. Stepanovna
    Afanasyev, B. Vladimirovich
    BONE MARROW TRANSPLANTATION, 2014, 49 : S318 - S318
  • [26] High prevalence of low bone mineral density in children with hurler syndrome after hematopoietic stem cell transplantation
    Polgreen, Lynda
    Petryk, Anna
    MOLECULAR GENETICS AND METABOLISM, 2009, 96 (02) : S35 - S35
  • [27] Impact of laronidase on shoulder, elbow, and hip range of motion in children with Hurler syndrome after hematopoietic cell transplantation
    Polgreen, Lynda E.
    Cabelka, Christine
    Lund, Troy
    Miller, Weston
    Orchard, Paul J.
    MOLECULAR GENETICS AND METABOLISM, 2015, 114 (02) : S94 - S94
  • [28] Comparison of Outcomes after Myeloablative Versus Reduced Intensity Conditioning Allogeneic Hematopoietic Cell Transplantation for Chronic Myeloid Leukemia
    Chhabra, Saurabh
    Ahn, Kwang Woo
    Hu, Zhen-Huan
    Jain, Sandeep
    Stuart, Robert K.
    Kalaycio, Matt
    Popat, Uday
    Sobecks, Ronald
    Alyea, Edwin, III
    Saber, Wael
    BLOOD, 2017, 130
  • [29] Outcomes after allogenic hematopoietic cell transplantation with nonmyeloablative or myeloablative conditioning regimens for treatment of lymphoma and chronic lymphocytic leukemia
    Sorror, Mohamed L.
    Storer, Barry E.
    Maloney, David G.
    Sandmaier, Brenda M.
    Martin, Paul J.
    Storb, Rainer
    BLOOD, 2008, 111 (01) : 446 - 452
  • [30] Hematopoietic Stem Cell Transplantation in Children with Sickle Cell Disease: Myeloablative Versus Reduced Intensity Conditioning
    Alsultan, Abdulrahman S.
    Basher, Enas
    Abujoub, Rodaina
    Essa, Mohammed F.
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2020, 26 (03) : S222 - S223