Volume 26, Issue 3 pp. 131-137
Research Article

CD34+ collection efficiency as a function of blood volumes processed in pediatric autologous peripheral blood stem cell collection

Leonid Dubrovsky

Corresponding Author

Leonid Dubrovsky

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

Division of Bone Marrow Transplantation, Children's National Medical Center, 111 Michigan Ave., NW, Washington DC 20010Search for more papers by this author
Edward C.C. Wong

Edward C.C. Wong

Division of Laboratory Medicine, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Evelio Perez-Albuerne

Evelio Perez-Albuerne

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Brett Loechelt

Brett Loechelt

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Naynesh Kamani

Naynesh Kamani

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Jane Sande

Jane Sande

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Kathy Mintz

Kathy Mintz

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

William and Shirley Howard Stem Cell Processing Laboratory, George Washington School of Medicine and Health Sciences, Washington DC

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Wendy Paul

Wendy Paul

Division of Laboratory Medicine, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Naomi L.C. Luban

Naomi L.C. Luban

Division of Laboratory Medicine, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Brian R. Rood

Brian R. Rood

Division of Oncology, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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Terry Fry

Terry Fry

Division of Bone Marrow Transplantation, Children's National Medical Center, Center for Cancer and Blood Disorders, Washington DC

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First published: 03 February 2011
Citations: 17

Abstract

Purpose:

To characterize the relationship between CD34+ collection efficiency and blood volumes processed in pediatric patients undergoing autologous peripheral blood stem cell (PBSC) collection.

Methods:

Retrospective 8-year (2001–2009) study of pediatric patients (n = 79) with neuroblastoma and central nervous system (CNS) tumors undergoing first day of autologous PBSC harvest using MNC program on the COBE Spectra (Caridian BCT, Lakewood, CO) was performed. Patients undergoing 0 to 2.9 BV (standard volume), 3 to 6 BV (large volume), and greater than 6 BV (ultra large volume) harvests were evaluated for CD34+ collection efficiency, diagnosis (neuroblastoma vs. nonneuroblastoma), disease type (primary vs. relapse), mobilization regimen, granulocyte colony stimulating factor (GCSF) dose, and apheresis complications.

Results:

CD34+ collection efficiencies (CE) for neuroblastoma patients were 67%, 50%, and 53% for standard (n = 14), large (n = 9), and ultra large (n = 5) volume harvests, respectively. Similarly, patients with nonneuroblastoma diagnoses had CD34+ CE of 63%, 55%, and 65% for low (n = 19), large (n = 27), and ultra large (n = 5) volume harvests, respectively. Weight, granulocyte colony stimulating factor (G-CSF) stimulation, type of mobilization, and apheresis complications (normalized by run time) were similar between the standard, large, and ultra large volume groups in patients with either neuroblastoma or nonneuroblastoma diagnoses.

Conclusions:

CD34+ collection efficiency in pediatric autologous PBSC collection on the first day of harvest does not decrease with higher numbers of blood volumes processed in patients with either neuroblastoma or nonneuroblastoma primary disease. These results indirectly indicate bone marrow CD34+ cell mobilization occurs with longer apheresis procedures in pediatric patients. J. Clin. Apheresis, 2011. © 2011 Wiley-Liss, Inc.

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