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Autologous Bone Marrow Transplantation - Blog Science Connections

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202 Autografting in Chronic Granulocytic Leukemia<br />

metaphases. After they received transplants of in vivo purged marrow<br />

containing, respectively, 1 and 2.9 x 10 4 thawed CFCI-GM cells/kg, engraftment<br />

was very prompt in both cases. After transplantation, one of the patients had a<br />

mixture of Ph 1 -positive and Ph 1 -negative cells for 4 months until the typical<br />

features of the chronic phase returned. After ABMT, the percentage of Ph 1 -<br />

negative marrow cells found in this patient never exceeded substantially the<br />

percentage of Ph 1 -negative cells transplanted. The other patient achieved<br />

"clinical" remission after transplantation and is still in continuous clinical<br />

remission 18 months after transplantation.<br />

Such a Ph 1 -negative status has previously been reported in patients with<br />

CGL in transformation undergoing autologous transplantation of marrow or<br />

blood cells (see review, 13). The latter case confirms the proliferative advantage<br />

of Ph 1 -negative precursors transplanted to the patient, an advantage that may<br />

be the result of selective cryoinjury of Ph 1<br />

-positive progenitors (14). The results<br />

observed in our patient differ from those of other reports in two remarkable<br />

aspects: the number of Ph 1 -positive cells present after transplantation was very<br />

low and the duration of clinical remission was very long, suggesting that the<br />

preclinical phase of CGL was restored. Moreover, autologous transplantation<br />

may have prolonged the chronic phase. This encouraging result was obtained<br />

in the one patient who received a transplant only 16 months after diagnosis of<br />

CGL (versus 18, 45, and 91 months for the other patients), so that ABMT, if<br />

used, should be considered early in the course of CGL ( 15).<br />

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Sanders JE, Singer J, Stewart P, Storb R, Sullivan K, Weiden PL, Witherspoon R. Ann Intern Med<br />

1986;104:155.<br />

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Braustet A. Exp Haematol 1983;1 l(Suppl 13):148.<br />

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First International Symposium, Dicke KA, Spitzer G, Zander AR, eds. The university of Texas<br />

M. D. Anderson Hospital and Tumor Institute at Houston, Houston, 1985:11.<br />

5. Reiffers J, Gorin NC, Michallet M, Maraninchi D, Herve P. Br J Haematol 1985;60:770.<br />

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8. Coulombel L, Kalousek DK, Eaves CJ, Gupta CM, Eaves AC. N Engl J Med 1983:308:1493.<br />

9. Goto T, Nishikori M, Arlin Z, Gee T, Kempin S, Burchenal J, Strife A, Wisniewski D, Lambek C,<br />

Jhanwar S, Chaganti R, Clarkson B. Blood 1982;59:793.<br />

10. Maraninchi D, Pico JL, Hartmann O, Gastaut JA, Kamonier D, HayatM, Mascret B, Beaujean F,<br />

Sebahoun G, Novakovitch G, Lemerle J, Carcassonne Y. Cancer Treat Rep 1986:70:445.<br />

11. Reiffers J, Marit G, David B, Chevaleyre J, Bernard P, Richaud P, Vezon G, Braustet A. <strong>Bone</strong><br />

<strong>Marrow</strong> <strong>Transplantation</strong> 1986;l(Suppl):370.

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