Summary:
The factors possibly affecting the collection of peripheral blood stem cells (PBSC) were evaluated in 104 de novo acute leukemia patients (66 myeloid and 38 lymphoblastic leukemias) in first cytological complete remission (CR); all patients achieved CR after first-line induction chemotherapy. The acute myeloid leukemia patients (AML) were given consolidation–mobilization chemotherapy with cytarabine, and daunoblastin or mitoxantrone or idarubicin; the acute lymphoblastic leukemia patients (ALL) were given consolidation–mobilization chemotherapy with cytarabine and etoposide. In all patients, the collection of PBSC was performed during recovery after giving consolidation chemotherapy and granulocyte colony-stimulating factor (G-CSF). Two main groups were considered according to the CD34+ cells × 106/kg b.w. collected, that is, poor mobilizers (PM), with a collection of <2 × 106/kg and good mobilizers, with a collection of >2 × 106/kg. Of 104 patients, 27 (25.9%) were PM; 20/27 had AML and 7/27 had ALL. At multivariate analysis, a lower CD34+ cells count premobilization chemotherapy (CD34 steady state), the presence of FUO (fever of unknown origin) or infection, and a lower number of CD34+ cells on the first day of collection correlated with poor mobilization. These results may enable early recognition of patients who may have poor mobilization, and aid selection of patients for different mobilization regimens.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Gratwohl A, Passweg J, Baldomero H et al. Blood marrow transplantation activity in Europe 1997: European Group for Blood Marrow Transplantation (EBMT). Bone Marrow Transplant 1999; 24: 231–245.
Korbling M, Fliedner TM, Holle R et al. Autologous blood stem cell (ABSCT) versus purged bone marrow transplantation (pABMT) in standard risk AML: influence of source and cell composition of the autograft on hematopoietic reconstitution and disease free survival. Bone Marrow Transplant 1991; 7: 343–349.
Sanz MA, De la Rubia J, Sanz GF et al. Busulfan plus cyclophosphamide followed by autologous blood stem cell transplantation for patients with acute myeloblastic leukaemia in first complete remission: a report from a single institution. J Clin Oncol 1993; 11: 1661–1667.
De la Rubia J, Sanz JF, Martin G et al. Autologous blood stem cell transplantation for acute myeloblastic leukaemia in first complete remission: intensification therapy before transplantation does not prolong disease-free survival. Haematologica 1999; 84: 125–132.
To LB, Roberts MM, Haylock DN et al. Comparison of haematological recovery times and supportive care requirements of autologous recovery phase peripheral blood stem cell transplant, autologous bone marrow transplant and allogeneic bone marrow transplants. Bone Marrow Transplant 1992; 9: 277–284.
Beyer J, Schwella N, Zingsem J et al. Hematopoietic rescue after high-dose chemotherapy using autologous peripheral-blood stem cells or bone marrow: a randomised comparison. J Clin Oncol 1995; 13: 1328–1335.
Besinger WI, Longin K, Appelbaum F et al. Peripheral blood stem cells (PBSCs) collected after recombinant granulocyte colony-stimulating factor (rhG-CSF): an analysis of factors correlating with the time of engraftment after transplantation. Br J Haematol 1994; 87: 825–831.
Weaver CH, Hazelton B, Birch R et al. An analysis of engraftment kinetics as a function of the CD34 content of peripheral blood stem cell collections in 692 patients after the administration of myeloablative chemotherapy. Blood 1995; 86: 3961–3969.
Kiss JE, Rybka WB, Winkelstein A et al. Relationship of CD34+ cell dose to early and late hematopoiesis following autologous peripheral blood stem cell transplantation. Bone Marrow Transplant 1997; 19: 303–310.
Haas R, Witt B, Mohle R et al. Sustained long-term hematopoiesis after myeloablative therapy with peripheral blood progenitor cell support. Blood 1995; 85: 3754–3761.
Ketterer N, Salles G, Raba M et al. High CD34(+) cell counts decrease hematologic toxicity of autologous peripheral blood progenitor cell transplantation. Blood 1998; 91: 3148–3155.
Alegre A, Tomas JF, Martinez-Chamorro C et al. Comparison of peripheral blood progenitor cell mobilization in patients with multiple myeloma: high dose cyclophosphamide plus GM-CSF versus G-CSF alone. Bone Marrow Transplant 1997; 20: 211–217.
Besinger W, Appelbaum F, Rowley S et al. Factors that influence collection and engraftment of autologous peripheral blood stem cells. J Clin Oncol 1995; 13: 2547–2555.
Watts MJ, Sullivan AM, Jamieson E et al. Progenitor cell mobilization after low-dose cyclophosphamide and granulocyte colony-stimulating factor: an analysis of progenitor cell quantity and quality and factors predictive for these parameters in 101 pre-treated patients with malignant lymphoma. J Clin Oncol 1997; 15: 535–546.
Moskowitz CH, Glasmann GR, Wuest D et al. Factors affecting mobilization of peripheral blood progenitor cells in patients with lymphoma. Clin Cancer Res 1998; 4: 311–316.
Sautois B, Fraipont V, Baudoux E et al. Peripheral blood progenitor cell collections in cancer patients: analysis of factors affecting the yields. Haematologica 1999; 84: 342–349.
Dreger P, Kloss M, Petersen B et al. Autologous progenitor cell transplantation: prior exposure to stem cell-toxic drug determines yield and engraftment of peripheral blood progenitor cell but not of bone marrow grafts. Blood 1995; 86: 3970–3978.
Kotasek D, Shepherd KM, Sage RE et al. Factors affecting blood stem collections following high-dose cyclophosphamide mobilization in lymphoma, myeloma and solid tumors. Bone Marrow Transplant 1992; 9: 11–17.
Carral A, De La Rubia J, Martin G et al. Factors influencing the collection of peripheral blood stem cells in patients with acute myeloblastic leukemia and non-myeloid malignancies. Leukaemia Res 2003; 27: 5–12.
Schelenk R, Dohner H, Pforsich M et al. Successful collection of peripheral blood progenitor cells in patients with acute myeloid leukaemia following early consolidation therapy with granulocyte colony-stimulating factor-supported high-dose cytarabine and mitoxantrone. Br J Haematol 1997; 99: 386–393.
Jowitt SN, Chang J, Morgenstern GR et al. Factors which affect the CFU-GM content of the peripheral blood haemopoietic progenitor cell harvests in patients with acute myeloid leukaemia. Br J Haematol 1998; 100: 668–694.
Moretti S, Dabusti M, Castagnari B et al. Comparison of single and dual platform methodologies for the estimation of CD34+ hematopoietic progenitor cells: correlation with colony assay. Int J Biol Markers 2002; 17: 259–267.
Drake M, Ranaghan L, Morris M et al. Analysis of the effect of prior therapy on progenitor cell yield: use of a chemotherapy scoring system. Br J Haematol 1997; 98: 745–749.
Fruehauf S, Schmitt K, Veldwijk R et al. Peripheral blood progenitor cell (PBPC) counts during steady-state haemopoiesis enable the estimation of the yield of mobilized PBPC after granulocyte colony-stimulating factor supported cytotoxic chemotherapy: an update on 100 patients. Br J Haematol 1999; 105: 786–794.
Diaz M, Sanchez-Garcia F, Lillo R et al. Large-volume leukapheresis in pediatric patients: pre-apheresis peripheral blood CD34+ cell count predicts progenitor cell yield. Haematologica 1999; 84: 32–35.
Benjamin RJ, Linsley L, Fountain B et al. Preapheresis peripheral blood CD34+ mononuclear cell counts as a predictor of progenitor cell yield. Transfusion 1997; 37: 79–85.
Elliot C, Samsom DM, Armitage S et al. When to harvest peripheral-blood stem cells after mobilization therapy: prediction of CD34-positive cell yield by preceding day CD34-positive concentration in peripheral blood. J Clin Oncol 1996; 14: 970–973.
Xiao W, Koizumi K, Nishio M et al. Tumor necrosis factor-alpha inhibits generation of glycophorine A+ cells by CD34+ cells. Exp Hematol 2002; 30: 1238–1247.
Carlo-Stella C, Tabilio A . Stem cell and stem cell transplantation. Haematologica 1996; 81: 573–587.
Ogawa M . Differentiation and proliferation of hemopoietic stem cells. Blood 1993; 81: 2844–2853.
Acknowledgements
This work was supported by Ministero dell'Istruzione dell'Università e della Ricerca (MIUR); we thank Ms MVC Pragnell, BA, for language assistance in the preparation of the manuscript.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Pastore, D., Specchia, G., Mestice, A. et al. Good and poor CD34+ cells mobilization in acute leukemia: analysis of factors affecting the yield of progenitor cells. Bone Marrow Transplant 33, 1083–1087 (2004). https://doi.org/10.1038/sj.bmt.1704437
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/sj.bmt.1704437
Keywords
This article is cited by
-
A novel small molecule CXCR4 antagonist potently mobilizes hematopoietic stem cells in mice and monkeys
Stem Cell Research & Therapy (2021)
-
G-CSF-primed BM for allogeneic SCT: revisited
Bone Marrow Transplantation (2015)
-
Prognostic value of CD34+ peak in peripheral blood during mobilization in intermediate-risk AML patients treated in first CR by autologous or allogeneic transplantation
Bone Marrow Transplantation (2012)
-
Proposed definition of ‘poor mobilizer’ in lymphoma and multiple myeloma: an analytic hierarchy process by ad hoc working group Gruppo ItalianoTrapianto di Midollo Osseo
Bone Marrow Transplantation (2012)
-
Plerixafor with and without chemotherapy in poor mobilizers: results from the German compassionate use program
Bone Marrow Transplantation (2011)