No Impact of Total or Myeloid Cd34+Cell Numbers on Neutrophil Engraftment and Transplantation-Related Mortality after Allogeneic Pediatric Bone Marrow Transplantation
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作者:
Pichler, Herbert
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Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Pichler, Herbert
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Witt, Volker
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Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Witt, Volker
[1
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Winter, Elisabeth
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Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Winter, Elisabeth
[1
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Boztug, Heidrun
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Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Boztug, Heidrun
[1
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Glogova, Evgenia
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St Anna Kinderkrebsforsch, Childrens Canc Res Inst, A-1090 Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Glogova, Evgenia
[2
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Poetschger, Ulrike
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St Anna Kinderkrebsforsch, Childrens Canc Res Inst, A-1090 Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Poetschger, Ulrike
[2
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Matthes-Martin, Susanne
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Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Matthes-Martin, Susanne
[1
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Fritsch, Gerhard
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St Anna Kinderkrebsforsch, Childrens Canc Res Inst, A-1090 Vienna, AustriaMed Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
Fritsch, Gerhard
[2
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机构:
[1] Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
[2] St Anna Kinderkrebsforsch, Childrens Canc Res Inst, A-1090 Vienna, Austria
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 x 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 x 106/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. 2014 American Society for Blood and Marrow Transplantation.
机构:
Univ Paris CIte, INSERM, UMR 976, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Bordenave, Jennifer
Gajda, Dorota
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Univ Paris Cite, Fac Pharm, UR 7537 BioSTM, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Gajda, Dorota
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Michonneau, David
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Vallet, Nicolas
Chevalier, Mathieu
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Univ Paris CIte, INSERM, UMR 976, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Chevalier, Mathieu
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Clappier, Emmanuelle
Lemaire, Pierre
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Hop St Louis, APHP, Lab Hematol, St Louis, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Lemaire, Pierre
Mathis, Stephanie
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Hop St Louis, APHP, Lab Hematol, St Louis, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Mathis, Stephanie
Robin, Marie
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Hop St Louis, Assistance Publ Hop Paris APHP, Hematol Greffe, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Robin, Marie
Xhaard, Alienor
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Hop St Louis, Assistance Publ Hop Paris APHP, Hematol Greffe, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Xhaard, Alienor
de Fontbrune, Flore Sicre
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Hop St Louis, Assistance Publ Hop Paris APHP, Hematol Greffe, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
de Fontbrune, Flore Sicre
Corneau, Aurelien
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Plateforme Cytometrie Pitie Salpetriere CyPS, UMS037 PASS, Paris, France
Sorbonne Univ, Fac Med, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Corneau, Aurelien
Caillat-Zucman, Sophie
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Univ Paris CIte, INSERM, UMR 976, Paris, France
Univ Paris Cite, UFR Med, Paris, France
Hop St Louis, APHP, Lab Immunol, St Louis, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Caillat-Zucman, Sophie
de Latour, Regis Peffault
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Hop St Louis, Assistance Publ Hop Paris APHP, Hematol Greffe, Paris, France
Univ Paris Cite, UFR Med, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
de Latour, Regis Peffault
Curis, Emmanuel
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Univ Paris Cite, Fac Pharm, UR 7537 BioSTM, Paris, France
Hop Lab, APHP, Lab Hematol, Paris, FranceUniv Paris CIte, INSERM, UMR 976, Paris, France
Curis, Emmanuel
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Socie, Gerard
JOURNAL OF CLINICAL INVESTIGATION,
2024,
134
(20):