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Autologous Bone Marrow Transplantation - Blog Science Connections

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Peripheral Stem Cell <strong>Transplantation</strong> 631<br />

lymphohematopoietic disorders in remission may be in favor of the stem<br />

cells, although this hypothesis is yet to be proved.<br />

ABSCT seems to be a viable treatment method in three types of settings.<br />

It can be used supportively, to augment the reconstitutive potency of<br />

quantitatively inadequate autologous marrow collection. It has demonstrated<br />

therapeutic activity against acute leukemia in CR, non-Hodgkin's lymphoma,<br />

and perhaps against resistant multiple myeloma. And it can be used<br />

prophylactically in persons who are at risk for severe radiation exposure or in<br />

those with a genetic predisposition for malignant lymphohematopoietic<br />

disorders.<br />

This study has shown that apheresis-derived hematopoietic stem cells<br />

are able to reconstitute hematopoiesis completely and permanently.<br />

Furthermore, if sufficient numbers of stem cells are transfused (more than<br />

1 -2 x 10 4 /kg b.w.), hematopoietic reconstitution occurs rapidly. At present,<br />

to enable hematopoietic stem cells to be collected efficiently, the patient must<br />

have been adequately pretreated cytotoxically. Other, and perhaps more<br />

effective, approaches for mobilizing hematopoietic stem cells into the<br />

peripheral blood are needed and are currently under investigation.<br />

ABSCT after myeloablative chemoradiotherapy promises an alternative<br />

approach to autologous bone marrow transplantation that provides additional<br />

safety because of low aplasia-related risks. The possible long-term benefit to<br />

the patients who receive the transplantation must be further proven, however,<br />

in additional clinical trials.<br />

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Verlag, Heidelberg, New York, 1978.<br />

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14. Juttner CA, To LB, Haylock DN, Branford A, Dyson P, Kimber RJ. ExpHematol 1986:14:465.<br />

15. Castaigne S, Calvo F, Douay L, Thomas F, Benbunan M, Gerota J, Degos L. Br J Haematol<br />

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16. Castaigne S, Tilly H, Leverger G, Lepage E, Bastit D, Miclea JM, Boiron M. 28th Annual<br />

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17. Tilly H, Bastit D, Lucet JC, Esperou H, Monconduit M, Piguet H. Lancet 1986;2:154.

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