Modeling Long-Term Erythropoietic Recovery After Allogeneic Stem Cell Transplants in Pediatric Patients
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作者:
von Asmuth, Erik G. J.
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Leiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, NetherlandsLeiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, Netherlands
von Asmuth, Erik G. J.
[1
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Mohseny, Alexander B.
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Leiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, NetherlandsLeiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, Netherlands
Mohseny, Alexander B.
[1
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Putter, Hein
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Leiden Univ, Med Ctr, Dept Med Stat, Leiden, NetherlandsLeiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, Netherlands
Putter, Hein
[2
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Schilham, Marco W.
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Leiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, NetherlandsLeiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, Netherlands
Schilham, Marco W.
[1
]
Lankester, Arjan C.
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Leiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, NetherlandsLeiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, Netherlands
Lankester, Arjan C.
[1
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机构:
[1] Leiden Univ, Willem Alexander Childrens Hosp, Med Ctr, Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Med Stat, Leiden, Netherlands
Long term erythropoietic reconstitution after allogeneic hematopoietic stem cell transplantation (alloHSCT) has not been extensively studied. We aimed to describe erythropoietic reconstitution as an indicator of long-term graft function by modeling hemoglobin levels during the first 3 years post HSCT in pediatric patients. We retrospectively included 414 patients and 11,957 measurements. The largest hemoglobin increase was at day 45 and levels reached a steady state at day 648 with a level of 7.48 mmol/L. In patients transplanted for hematological malignancies hemoglobin levels normalized faster (p < 0.0001). Increasing patient age correlated with faster recovery (p < 0.0001), while donor age had no influence. Conditioning, donor type and graft source did not influence recovery significantly. In the ABO mismatched group there was a transient negative effect on hemoglobin levels, and a delay in reticulocyte recovery (21 vs. 19 days; p = 0.012). In contrast, hemoglobin levels reached a higher plateau beyond 9 months in these patients (p < 0.0001). After alloHSCT, experiencing a CMV reactivation negatively affected reconstitution (p = 0.034), while EBV reactivations and acute graft vs. host disease did not. In summary, erythropoietic recovery was mainly influenced by patient factors and primary disease, and less influenced by donor factors.
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Kim, Jiyoung
Mo, Hyejin
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Mo, Hyejin
Chung, Chris Tea Young
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Chung, Chris Tea Young
Kim, Hyo Kee
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Kim, Hyo Kee
Ko, Hyunmin
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Ko, Hyunmin
Han, Ahram
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Han, Ahram
Min, Sangil
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Min, Sangil
Ha, Jongwon
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Seoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
Seoul Natl Univ, Dept Surg, Coll Med, Seoul, South KoreaSeoul Natl Univ Hosp, Dept Surg, Seoul, South Korea
机构:
Hop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Univ Paris Diderot, Sorbonne Paris Cite, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Itzykson, Raphael
Robin, Marie
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Hop St Louis, AP HP, Serv Hematol Greffe, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Robin, Marie
Moins-Teisserenc, Helene
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Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
Hop St Louis, AP HP, Immunol Lab, Paris, France
Inst Univ Hematol, Inserm UMRS 1160, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Moins-Teisserenc, Helene
Delord, Marc
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机构:
Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
Inst Univ Hematol, Plateforme Bioinformat & Biostat, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Delord, Marc
Busson, Marc
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Hop St Louis, AP HP, Immunol Lab, Paris, France
Inst Univ Hematol, Inserm UMRS 1160, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Busson, Marc
Xhaard, Alienor
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Hop St Louis, AP HP, Serv Hematol Greffe, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Xhaard, Alienor
de Fontebrune, Flore Sicre
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Hop St Louis, AP HP, Serv Hematol Greffe, Paris, France
Univ Paris Diderot, Sorbonne Paris Cite, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
de Fontebrune, Flore Sicre
de latour, Regis Peffault
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Hop St Louis, AP HP, Serv Hematol Greffe, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France
de latour, Regis Peffault
Toubert, Antoine
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Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
Hop St Louis, AP HP, Immunol Lab, Paris, France
Inst Univ Hematol, Inserm UMRS 1160, Paris, FranceHop St Louis, AP HP, Serv Hematol Greffe, Paris, France