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VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...

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sion in this arm. The evolution of WBC and PMN counts is remarkable since following<br />

a first wave of neutrophils which occurred within the same time than the<br />

complete recovery in arm A, a secondary aplasia developed, unresponsive to a<br />

reintroduction of rh GM-CSF given subcutaneously. Prolonged<br />

thrombocytopenia was observed in these patients, without the first wave observed<br />

on the WBC and PMN curves. The history of these three patients was<br />

uninspired when looking at parameters such as age, CBC parameters before<br />

graft, history of prior marrow involvement, duration of previous chemotherapy,<br />

prior radiotherapy which could have generated a marrow micro-environment<br />

impairment. Opposite, the recovery from neutropenia and of thrombocytopenia<br />

was peculiarly rapid and steady in arm A, whereas the number of cells grafted<br />

were comparable in terms of nucleated cells and CFU-GM. The absence of difference<br />

between the two groups of patients in terms of clinical parameters,<br />

therapeutic procedures and number of CPU GM grafted suggests that PBSC collected<br />

in arm B are more mature than in arm A. The number of 7-day CFU GM<br />

assay does not reflect the number of pluripotent stem cells and is dependent of<br />

the harvesting procedure.<br />

CONCLUSION<br />

Rh GM-CSF can mobilize PBSC for collection by cytapheresis. Nevertheless,<br />

mobilization of pluripotent stem cells is dependent on the duration of stimulation<br />

by growth factors. One must be cautious when comparing the number of<br />

PBSC collected with various harvesting procedures evaluated by the 7-day CFU<br />

GM assay.<br />

REFERENCES<br />

1. Verdonck LF, Dekker AW, Van Kempen ML et al. Intensive cytotoxic therapy<br />

followed by autologous bone marrow transplantation for non-Hodgkin's lymphoma<br />

of high grade malignancy. Blood, 1985,65,894-989.<br />

2. Kessinger A, Armitage JO, Landark et al. <strong>Autologous</strong> peripheral hematopoietic stem<br />

cell transplantation restores hematopoietic function following marrow ablative<br />

therapy. Blood 1988, 71,723-727.<br />

3. Kessinger A, Armitage JO, Landark et al. Reconstitution of human hematopoietic<br />

function with autologous cryopreserved circulating stem cells. Exp Hematol 1986,<br />

71, 723-727.<br />

4. Kotasek D, Shepherd KM, Sage RE et al. Factors affecting blood stem cell collections<br />

following high-dose cyclophosphamide mobilization in lymphoma, myeloma and<br />

solid tumors. <strong>Bone</strong> <strong>Marrow</strong> <strong>Transplantation</strong> 1992,9,11-17.<br />

5. Kessinger A, Armitage JO. High dose therapy with autologous peripheral blood<br />

stem cell transplantation for patients with lymphoma metastatic to bone marrow.<br />

Proceedings of the 24th ASCO meeting. J Clin Oncol 1988,7,223.<br />

6. Reiffers J, Leverger G, Marit Get al. Haematopoietic reconstitution after autologous<br />

blood stem cell transplantation: current controversies (Gale RP, Champlin eds) Allan<br />

Liss, New York, 1988,313-320.<br />

7. Morstyn G, Campbell L, Souza LM et al. Effect of recombinant granulocyte-macrophage<br />

colony stimulating factor on neutropenia induced by cytotoxic chemotherapy.<br />

Lancet 1988, ii, 667-672.<br />

8. Brandt S J, Peters WP, Atwater SK et al. Effects of recombinant granulocyte-macrophage<br />

colony stimulating factor on haematopoietic reconstitution after high dose<br />

chemotherapy and autologous transplantation. N Eng J Med 1988,318,869-876.<br />

SIXTH INTERNATIONAL SYMPOSIUM ON AUTOLOGOUS BONE MARROW TRANSPLANTATION 243

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