Literature DB >> 24492145

No impact of total or myeloid Cd34+ cell numbers on neutrophil engraftment and transplantation-related mortality after allogeneic pediatric bone marrow transplantation.

Herbert Pichler1, Volker Witt1, Elisabeth Winter1, Heidrun Boztug1, Evgenia Glogova2, Ulrike Pötschger2, Susanne Matthes-Martin1, Gerhard Fritsch3.   

Abstract

Although the influence of transplanted bone marrow (BM) CD34+ cells on neutrophil engraftment (NE) and transplantation outcomes has been discussed controversially, thresholds between 2 and 4 × 10(6)/kg CD34+ cells are commonly accepted. This has substantial consequences for a donor in terms of BM volume to be collected, which frequently covers up to 15 to 20 mL/kg. As the BM CD34+ compartment contains varying fractions of CD34+/CD19+ B lymphoid progenitors, we tested the hypothesis that the infused CD34+/CD45dim/CD19-/CD10- myeloid stem cells might reliably predict NE in 94 children who received BM from 37 HLA-identical sibling donors (MSD) and 57 matched unrelated donors after myeloablative conditioning. The grafts contained a median of 3.6 × 10(6)/kg total CD34+ cells, which consisted of a median of 73% myeloid CD34+ cells and 27% B lymphoid progenitors. Grafts from donors <15 years old yielded significantly lower myeloid fractions compared with grafts from older donors (P < .001). All patients achieved sustained NE after median 20 (range, 11 to 40) days. By multivariate analysis, neither the number of total CD34+ cells (P = .605) nor of myeloid CD34+ cells (P = .981) correlated with NE, whereas transplantation from MSD (hazard ratio [HR] 3.51; P = .019) and the administration of granulocyte colony-stimulating factor (HR 2.24; P = .002) remained independent factors associated with earlier NE. Furthermore, neither total nor myeloid CD34+ cell quantities were associated with incidences of severe infections before NE (P = .271 and P = .132) or transplantation-related mortality (TRM) at day +100 (P = .294 and P = .490). Taking into account that the number of transplanted total CD34+ or myeloid CD34+ cells does not seem to have a relevant impact on time to NE, sepsis rates, or TRM, the need of certain threshold cell numbers should be revisited, at least for pediatric MSD.
Copyright © 2014 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CD34+ cell dose; Graft composition; Hematopoietic recovery; Pediatric stem cell transplantation

Mesh:

Substances:

Year:  2014        PMID: 24492145     DOI: 10.1016/j.bbmt.2014.01.026

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  2 in total

1.  Delayed platelet recovery and mortality after allogeneic stem cell transplantation in children.

Authors:  Joseph R Wells; Guolian Kang; Ali Y Suliman; Ying Li; Salem Akel; Brandon Triplett; Ashok Srinivasan
Journal:  Bone Marrow Transplant       Date:  2022-05-28       Impact factor: 5.174

2.  Allogeneic hematopoietic stem cell transplantation from unrelated donors is associated with higher infection rates in children with acute lymphoblastic leukemia-A prospective international multicenter trial on behalf of the BFM-SG and the EBMT-PDWP.

Authors:  Herbert Pichler; Anita Lawitschka; Evgenia Glogova; Andre M Willasch; Irene von Luettichau; Thomas Lehrnbecher; Susanne Matthes-Martin; Peter Lang; Peter Bader; Karl W Sykora; Johanna Schrum; Bernhard Kremens; Karoline Ehlert; Michael H Albert; Michaela Kuhlen; Roland Meisel; Tayfun Guengoer; Brigitte Strahm; Bernd Gruhn; Ansgar Schulz; Wilhelm Woessmann; Ulrike Poetschger; Christina Peters
Journal:  Am J Hematol       Date:  2019-05-29       Impact factor: 10.047

  2 in total

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