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De Witte et al.<br />

hematopoietic engraftment was also slower in these seven patients, but all patients<br />

engrafted except for one patient who died early before engraftment of treatment-<br />

related causes. Two patients were alive <strong>and</strong> well at 10 <strong>and</strong> 28 months after<br />

autoBMT. 30<br />

Demuynck et al. 33<br />

investigated the feasibility of collecting peripheral stem cells<br />

in 11 patients with myelodysplasia. This resulted in seven patients with an adequate<br />

yield (>1 X 10 6<br />

/kg) of CD34 cells. 32<br />

Three patients with a normal to excellent stem<br />

cell harvest were demonstrated to be polyclonal by PCR techniques based on Xchromosome<br />

inactivation patterns. 27<br />

Sixteen patients received <strong>autologous</strong><br />

peripheral <strong>blood</strong> SCT in a prospective study of the EORTC Leukemia Cooperative<br />

Group <strong>and</strong> the EBMT. 34<br />

Peripheral stem calls were collected during the recovery<br />

phase of the first consolidation course using 300 ug filgrastim (subcutaneously)<br />

daily until completion of PBSC collections. Preliminary data indicate that the<br />

repopulation was much faster compared with autoBMT. 27<br />

' 33-35<br />

Autologous SCT<br />

has emerged as a treatment option for patients with myelodysplastic syndromes or<br />

acute myeloid leukemia evolved from MDS. Only patients who are in complete<br />

remission after intensive chemotherapy are considered as c<strong>and</strong>idates for autoSCT.<br />

About one-quarter of the patients with <strong>autologous</strong> stem cells may be free of disease<br />

for 3 years or longer. The high treatment-related mortality contributes substantially<br />

to this result, which is inferior to the results obtained by <strong>transplantation</strong> for de novo<br />

AML. Prospective, multicenter studies may reveal which categories of patients<br />

with MDS will benefit from intensive chemotherapy followed by autoSCT. This<br />

treatment approach has to be assessed against the merits <strong>and</strong> disadvantages of<br />

allogeneic stem cell <strong>transplantation</strong> with donors other than HLA-identical siblings.<br />

REFERENCES<br />

1. Mufti GJ, Stevens JR, Oscier DG, et al.: Myelodysplastic syndromes, a scoring system<br />

with prognostic significance. Br J Haematol 59:425-433, 1985.<br />

2. Kantarjian HM, Keating MJ, Walters RS, et al.: Therapy-related leukemia <strong>and</strong> myelodys­<br />

plastic syndrome: Clinical, cytogenetic, <strong>and</strong> prognostic features. / Clin Oncol<br />

4:1748-1757,1986.<br />

3. Greenberg P, Cox C, LeBeau MM, et al.: International Workshop risk analysis system<br />

for evaluating prognosis in myelodysplastic syndromes. Blood 89:2077-2088,1997.<br />

4. De Witte T, Zwaan F, Hermans J, et al.: Allogeneic bone <strong>marrow</strong> <strong>transplantation</strong> for sec­<br />

ondary leukaemia <strong>and</strong> myelodysplastic syndrome: A survey by the Leukaemia Working<br />

Party of the European Bone Marrow Transplantation Group (EBMTG). Br J Haematol<br />

74:151-157,1990.<br />

5. De Witte T, Gratwohl A: Bone <strong>marrow</strong> <strong>transplantation</strong> for myelodysplastic syndrome <strong>and</strong><br />

secondary leukaemias. Annotation. Br J Haematol 84:361-367, 1993.<br />

6. Anderson JE, Appelbaum FR, Fisher LD, et al.: Allogeneic bone <strong>marrow</strong> <strong>transplantation</strong><br />

for 93 patients with myelodysplastic syndrome. Blood 82:677-681, 1993.<br />

43

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