Journal of Clinical Oncology, Vol 12, 1693-1702, Copyright © 1994 by American Society of Clinical Oncology
Development of a simplified single-apheresis approach for peripheral- blood progenitor-cell transplantation in previously treated patients with lymphoma
HM Jones, SA Jones, MJ Watts, A Khwaja, W Mills, A Fielding, AH Goldstone and DC Linch
Department of Haematology, University College London Medical School, England.
PURPOSE: The aims of this study were to develop a simplified, safe, and
cost-effective peripheral-blood progenitor-cell (PBPC) mobilization
protocol. PATIENTS AND METHODS: Twenty-six patients with relapsed or
resistant lymphomas were entered onto a sequential cohort study in which
schedules of various granulocyte colony-stimulating factor (G- CSF) were
administered after cyclophosphamide 1.5 g/m2. Hematologic recovery after
high-dose carmustine (BCNU) etoposide, cytarabine, and melphalan (BEAM)
chemotherapy was compared with that of 46 patients who received autologous
bone marrow transplantation (ABMT) without growth factors and 28 patients
who received ABMT followed by G-CSF. RESULTS: When G-CSF (10
micrograms/kg/d) was administered from the day after the cyclophosphamide,
neutropenia developed on day 8 followed by an abrupt increase in the WBC
count. The optimal time for PBPC harvesting was the day on which the
postnadir WBC count was greater than 8.0 x 10(9)/L, as shown by CD34+ cell
counts and granulocytic-macrophage colony-forming cell (GM-CFC) assays. The
reproducibility of the response was such that routine monitoring of CD34+
cell counts and GM-CFC was not necessary. A single leukapheresis on this
day was adequate for prompt hematologic engraftment, and posttransplant
G-CSF made little further impact on the rapid recovery. Compared with both
control groups, the use of PBPC led to more rapid neutrophil recovery,
markedly accelerated platelet recovery, less use of antimicrobial agents
and parenteral nutrition, and more than 10 days earlier discharge from
hospital. All of these differences were highly significant (P < .01).
CONCLUSION: A simplified mobilization protocol is described that requires
only one apheresis to achieve rapid hematologic engraftment.

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