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Outcomes of patients with severe combined immunodeficiency treated with hematopoietic stem cell transplantation with and without preconditioning.
Patel, Niraj C; Chinen, Javier; Rosenblatt, Howard M; Hanson, I Celine; Krance, Robert A; Paul, Mary E; Abramson, Stuart L; Noroski, Lenora M; Davis, Carla M; Seeborg, Filiz O; Foster, Samuel B; Leung, Kathryn S; Brown, Betty S; Ritz, Jerome; Shearer, William T.
Affiliation
  • Patel NC; Department of Pediatrics, Section of Allergy and Immunology, Baylor College of Medicine, Texas Children's Hospital, Houston, Tex 77039, USA.
J Allergy Clin Immunol ; 124(5): 1062-9.e1-4, 2009 Nov.
Article in En | MEDLINE | ID: mdl-19895994
ABSTRACT

BACKGROUND:

The effect of pretransplantation conditioning on the long-term outcomes of patients receiving hematopoietic stem cell transplantation for severe combined immunodeficiency (SCID) has not been completely determined.

OBJECTIVE:

We sought to assess the outcomes of 23 mostly conditioned patients with SCID and compare their outcomes with those of 25 previously reported nonconditioned patients with SCID who underwent transplantation.

METHODS:

In the present study we reviewed the medical records of these 23 consecutive, mostly conditioned patients with SCID who underwent transplantation between 1998 and 2007.

RESULTS:

Eighteen patients (median age at transplantation, 10 months; range, 0.8-108 months) received haploidentical mismatched related donor, matched unrelated donor, or mismatched unrelated donor transplants, 17 of whom received pretransplantation conditioning (with 1 not conditioned); 13 (72%) patients engrafted with donor cells and survive at a median of 3.8 years (range, 1.8-9.8 year); 5 (38%) of 13 patients require intravenous immunoglobulin; and 6 of 6 age-eligible children attend school. Of 5 recipients (median age at transplantation, 7 months; range, 2-23 months) of matched related donor transplants, all 5 engrafted and survive at a median of 7.5 years (range, 1.5-9.5 year), 1 recipient requires intravenous immunoglobulin, and 3 of 3 age-eligible children attend school. Gene mutations were known in 16 cases mutation in the common gamma chain of the IL-2 receptor (IL2RG) in 7 patients, mutation in the alpha chain of the IL-7 receptor (IL7RA) in 4 patients, mutation in the recombinase-activating gene (RAG1) in 2 patients, adenosine deaminase deficiency (ADA) in 2 patients, and adenylate kinase 2 (AK2) in 1 patient. Early outcomes and quality of life of the previous nonconditioned versus the present conditioned cohorts were not statistically different, but longer-term follow-up is necessary for confirmation.

CONCLUSIONS:

Hematopoietic stem cell transplantation in patients with SCID results in engraftment, long-term survival, and a good quality of life for the majority of patients with or without pretransplantation conditioning.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Severe Combined Immunodeficiency / Hematopoietic Stem Cell Transplantation / Transplantation Conditioning Aspects: Patient_preference Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: J Allergy Clin Immunol Year: 2009 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Severe Combined Immunodeficiency / Hematopoietic Stem Cell Transplantation / Transplantation Conditioning Aspects: Patient_preference Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: J Allergy Clin Immunol Year: 2009 Document type: Article Affiliation country: United States