Excellent survival after sibling or unrelated donor stem cell transplantation for chronic granulomatous disease

Caridad A. Martinez, Sweta Shah, William T. Shearer, Howard M. Rosenblatt, Mary E. Paul, Javier Chinen, Kathryn S. Leung, Alana Kennedy-Nasser, Malcolm K. Brenner, Helen E. Heslop, Hao Liu, Meng Fen Wu, Imelda C. Hanson, Robert A. Krance

Research output: Contribution to journalArticle

47 Scopus citations

Abstract

Background: Matched related donor (MRD) hematopoietic stem cell transplantation (HSCT) is a successful treatment for chronic granulomatous disease (CGD), but the safety and efficacy of HSCT from unrelated donors is less certain. Objective: We evaluated the outcomes and overall survival in patients with CGD after HSCT. Methods: We report the outcomes for 11 children undergoing HSCT from an MRD (n = 4) or an HLA-matched unrelated donor (MUD) (n = 7); 9 children were boys, and the median age was 3.8 years (range, 1-13 years). We treated both X-linked (n = 9) and autosomal recessive (n = 2) disease. Nine children had serious clinical infections before transplantation. The conditioning regimens contained busulfan, cyclophosphamide, cytarabine, or fludarabine according to the donor used. All patients received alemtuzumab (anti-CD52 antibody). Additional graft-versus-host disease (GvHD) prophylaxis included cyclosporine and methotrexate for MUD recipients and cyclosporine and prednisone for MRD recipients. Results: Neutrophil recovery took a median of 16 days (range, 12-40 days) and 18 days (range, 13-24 days) for MRD and MUD recipients, respectively. Full donor neutrophil engraftment occurred in 9 patients, and 2 had stable mixed chimerism; all patients had sustained correction of neutrophil oxidative burst defect. Four patients had grade I skin acute GVHD responding to topical treatment. No patient had grade II to IV acute GvHD or chronic GvHD. All patients are alive between 1 and 8 years after HSCT. Conclusion: For CGD, equivalent outcomes can be obtained with MRD or MUD stem cells, and HSCT should be considered an early treatment option.

Original languageEnglish (US)
Pages (from-to)176-183
Number of pages8
JournalJournal of Allergy and Clinical Immunology
Volume129
Issue number1
DOIs
StatePublished - Jan 1 2012
Externally publishedYes

Keywords

  • Chronic granulomatous disease
  • bone marrow transplantation
  • graft-versus-host disease
  • primary immunodeficiencies

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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    Martinez, C. A., Shah, S., Shearer, W. T., Rosenblatt, H. M., Paul, M. E., Chinen, J., Leung, K. S., Kennedy-Nasser, A., Brenner, M. K., Heslop, H. E., Liu, H., Wu, M. F., Hanson, I. C., & Krance, R. A. (2012). Excellent survival after sibling or unrelated donor stem cell transplantation for chronic granulomatous disease. Journal of Allergy and Clinical Immunology, 129(1), 176-183. https://doi.org/10.1016/j.jaci.2011.10.005