Peripheral blood stem cell (PBSC) mobilization and transplantation after fludarabine therapy in chronic lymphocytic leukaemia (CLL): a report of the European Blood and Marrow Transplantation (EBMT) CLL subcommittee on behalfof the EBMT Chronic Leukaemias Working Party (CLWP)
M. Michallet et al., Peripheral blood stem cell (PBSC) mobilization and transplantation after fludarabine therapy in chronic lymphocytic leukaemia (CLL): a report of the European Blood and Marrow Transplantation (EBMT) CLL subcommittee on behalfof the EBMT Chronic Leukaemias Working Party (CLWP), BR J HAEM, 108(3), 2000, pp. 595-601
We performed a survey from 122 centres of the European Group of Blood and M
arrow Transplantation (EBMT) concerning peripheral blood stem cell (PBSC) m
obilization after fludarabine treatment of patients with chronic lymphocyti
c leukaemia (CLL). A total of 101 leucaphereses from 29 patients was perfor
med. The median cell numbers collected were: CD34+ cells, 2.2 x 10(6)/kg (0
.1-15.3); granulocyte-macrophage colony-forming units (GM-CFU), 4.29 x 10(4
)/kg (0.4-177); and mononuclear cells, 6.4 x 10(8)/kg (1.3-63). In univaria
te and multivariate analyses, the numbers of cells collected were not signi
ficantly influenced by the nature of mobilizing regimen and there was a tre
nd towards the collection of a higher number of CD34+ cells from patients w
ho received fludarabine only before mobilization. There was a significant c
orrelation between the median number of CD34+ cells collected and the numbe
r of courses of fludarabine (higher CD34+ cell numbers were related to more
than six courses) and the interval between the last dose of fludarabine an
d the start of mobilizing therapy (higher CD34+ cell numbers were related t
o a delay greater than or equal to 2 months). Sixteen patients have subsequ
ently undergone autologous transplantation and showed rapid engraftment. In
conclusion, the results reported favour early stem cell mobilization in CL
L patients who are in remission after first-line therapy. However, attentio
n should be given to the timing of mobilization with respect to the time si
nce the last dose of fludarabine.