Fm. Uckun et al., CELLULAR EXPRESSION OF ANTIAPOPTOTIC BCL-2 ONCOPROTEIN IN NEWLY-DIAGNOSED CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA - A CHILDRENS CANCER GROUP-STUDY, Blood, 89(10), 1997, pp. 3769-3777
We found a marked variation in BCL-2 oncoprotein expression levels of
primary leukemic cells from 338 children with newly diagnosed acute ly
mphoblastic leukemia (ALL). None of the high-risk features predictive
of poor treatment outcome in childhood ALL, such as older age, high wh
ite blood cell (WBC) count, organomegaly, T-lineage immunophenotype, a
bility of leukemic cells to cause overt leukemia in severe combined im
munodeficient (SCID) mice, presence of MLL-AF4, and BCR-ABL fusion tra
nscripts were associated with high levels of BCL-2 expression, overall
, high BCL-2 levels were not associated with slow early response, fail
ure to achieve complete remission, or poor event-free survival. High B
CL-2 levels in primary leukemic cells predicted slow early response on
ly in T-lineage ALL patients, which comprised approximately 15% of the
total patient population. Even for this small subset of patients, the
level of BCL-2 expression did not have a significant impact an the sh
ortterm event-free survival. (C) 1997 by The American Society of Hemat
ology.