Cytogenetic response to autografting in chronic myelogenous leukemia correlates with the amount of BCR-ABL positive cells in the graft (vol 28, pg 104, 2000)
Mt. Corsetti et al., Cytogenetic response to autografting in chronic myelogenous leukemia correlates with the amount of BCR-ABL positive cells in the graft (vol 28, pg 104, 2000), EXP HEMATOL, 28(3), 2000, pp. 353-353
Objective. An important step in successful autografting of patients with ch
ronic myelogenous leukemia is the delivery of a leukemia-free graft. We con
ducted this study to determine whether the cytogenetic response after autog
rafting was correlated with the number of BCR ABL-positive cells present wi
thin the stem cell grafts.
Materials and Methods. By BCR-ABL mRNA quantification, we studied the seria
l pheresis products from 10 Philadelphia (Ph)-positive patients who receive
d ICE/mini-ICE mobilization therapy and underwent autologous stem cell tran
splantation. We correlated the residual disease within the graft reinfused
with the cytogenetic response following transplantation, taking into consid
eration those responses that lasted 12 months or more.
Results. Thirty-two patients received a graft with 0-35% Ph-metaphases and
19 received a graft with BCR-ABL/ABL ratio less than or equal to 0.01. Afte
r a median of 27 months (range, 12-50) from transplant, 18 patients achieve
d complete or major cytogenetic response lasting at least 12 months, and 14
of them (78%) received a graft with BCR-ABL/ABL ratio less than or equal t
o 0.01 (range, 0.0003-0.01). Twenty-two patients experienced short-lived re
sponses or had >35% Ph-positive cells in the marrow after transplant, but o
nly 5 of them (23%) had a graft with BCR-ABL/ABL ratio less than or equal t
o 0.01 (range, 0.001-0.01). Therefore, we found a strong association betwee
n a BCR-ABL/ABL ratio less than or equal to 0.01 and the achievement of com
plete or major cytogenetic remission after autografting (chi(2) test, p = 0
.0001). Patients reinfused with grafts contaminated at low levels with leuk
emic cells also showed a longer duration of the response (log-rank test, p
= 0.0009). Eleven patients were reinfused with the lowest level of contamin
ated stem cell collections, according to the BCR-ABL/ABL ratio. None of the
se patients experienced prolonged neutropenia or thrombocytopenia following
stem cell reinfusion and nine of them had longlasting complete or major cy
togenetic responses after transplant.
Conclusion. This study demonstrates that the number of BCR-ABL positive cel
ls present in a stem cell graft is an important predictive factor for the a
chievement and the duration of cytogenetic response after autografting. (C)
2000 International Society for Experimental Hematology. Published by Elsev
ier Science Inc.