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Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention

Peripheral Blood Stem Cells (PBSC) are usually mobilized using granulocyte colony stimulating factor (G-CSF) with or without chemotherapy. With the emergence of newer mobilizing agents, predicting poor mobilization may allow early intervention and prevent the costs and complications associated with...

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Autores principales: Sinha, S, Gastineau, D, Micallef, I, Hogan, W, Ansell, S, Buadi, F, Dingli, D, Dispenzieri, A, Gertz, M, Greiner, C, Hayman, S, Inwards, D, Johnston, P, Lacy, M, Litzow, M, Porrata, L, Winters, JL., Kumar, S
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021104/
https://www.ncbi.nlm.nih.gov/pubmed/20935680
http://dx.doi.org/10.1038/bmt.2010.236
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author Sinha, S
Gastineau, D
Micallef, I
Hogan, W
Ansell, S
Buadi, F
Dingli, D
Dispenzieri, A
Gertz, M
Greiner, C
Hayman, S
Inwards, D
Johnston, P
Lacy, M
Litzow, M
Porrata, L
Winters, JL.
Kumar, S
author_facet Sinha, S
Gastineau, D
Micallef, I
Hogan, W
Ansell, S
Buadi, F
Dingli, D
Dispenzieri, A
Gertz, M
Greiner, C
Hayman, S
Inwards, D
Johnston, P
Lacy, M
Litzow, M
Porrata, L
Winters, JL.
Kumar, S
author_sort Sinha, S
collection PubMed
description Peripheral Blood Stem Cells (PBSC) are usually mobilized using granulocyte colony stimulating factor (G-CSF) with or without chemotherapy. With the emergence of newer mobilizing agents, predicting poor mobilization may allow early intervention and prevent the costs and complications associated with remobilization. We retrospectively evaluated a cohort of 1556 patients seen between January 2000 and December 2008 with Multiple Myeloma (MM) (565; 36%), Non-Hodgkin’s Lymphoma (NHL) (562; 36%), Amyloidosis (345; 22%) or Hodgkin’s disease (HD) (94; 6%) initially mobilized with single agent G-CSF. Sensitivity-specificity analysis was used to identify ideal peripheral blood CD34 count (PB-CD34) cut-points that predicted successful collection. In patients with plasma-cell disorders a PB-CD34 of 11/uL, 17/uL, 21/uL, and 28/uL by day 4 or 5 were required to collect a target of 2, 4, 8 or 12 million/kg respectively. A CD34 yield <0.8 million cells/kg on first apheresis also predicted for <2 million CD34/kg. For patients with NHL or HD, a PB-CD34 <6/uL and <15/uL on day 4 or 5 predicted failure to achieve a target collection of 2 and 4 million/kg respectively. This study suggests that PB-CD34 thresholds should be based on collection target to allow for early intervention and prevent collection failures.
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spelling pubmed-30211042012-01-01 Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention Sinha, S Gastineau, D Micallef, I Hogan, W Ansell, S Buadi, F Dingli, D Dispenzieri, A Gertz, M Greiner, C Hayman, S Inwards, D Johnston, P Lacy, M Litzow, M Porrata, L Winters, JL. Kumar, S Bone Marrow Transplant Article Peripheral Blood Stem Cells (PBSC) are usually mobilized using granulocyte colony stimulating factor (G-CSF) with or without chemotherapy. With the emergence of newer mobilizing agents, predicting poor mobilization may allow early intervention and prevent the costs and complications associated with remobilization. We retrospectively evaluated a cohort of 1556 patients seen between January 2000 and December 2008 with Multiple Myeloma (MM) (565; 36%), Non-Hodgkin’s Lymphoma (NHL) (562; 36%), Amyloidosis (345; 22%) or Hodgkin’s disease (HD) (94; 6%) initially mobilized with single agent G-CSF. Sensitivity-specificity analysis was used to identify ideal peripheral blood CD34 count (PB-CD34) cut-points that predicted successful collection. In patients with plasma-cell disorders a PB-CD34 of 11/uL, 17/uL, 21/uL, and 28/uL by day 4 or 5 were required to collect a target of 2, 4, 8 or 12 million/kg respectively. A CD34 yield <0.8 million cells/kg on first apheresis also predicted for <2 million CD34/kg. For patients with NHL or HD, a PB-CD34 <6/uL and <15/uL on day 4 or 5 predicted failure to achieve a target collection of 2 and 4 million/kg respectively. This study suggests that PB-CD34 thresholds should be based on collection target to allow for early intervention and prevent collection failures. 2010-10-11 2011-07 /pmc/articles/PMC3021104/ /pubmed/20935680 http://dx.doi.org/10.1038/bmt.2010.236 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Sinha, S
Gastineau, D
Micallef, I
Hogan, W
Ansell, S
Buadi, F
Dingli, D
Dispenzieri, A
Gertz, M
Greiner, C
Hayman, S
Inwards, D
Johnston, P
Lacy, M
Litzow, M
Porrata, L
Winters, JL.
Kumar, S
Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention
title Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention
title_full Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention
title_fullStr Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention
title_full_unstemmed Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention
title_short Predicting Peripheral Blood Stem Cell Harvest Failure Using Circulating CD34 Levels: Developing Target-Based Cut-Points for Early Intervention
title_sort predicting peripheral blood stem cell harvest failure using circulating cd34 levels: developing target-based cut-points for early intervention
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021104/
https://www.ncbi.nlm.nih.gov/pubmed/20935680
http://dx.doi.org/10.1038/bmt.2010.236
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