DETECTION OF A DORMANT 20Q- LEUKEMIA CLONE IN BONE-MARROW CULTURES WITH HEMATOPOIETIC GROWTH-FACTORS - IMPLICATIONS FOR SECONDARY LEUKEMIA POSTTRANSPLANT
I. Redei et al., DETECTION OF A DORMANT 20Q- LEUKEMIA CLONE IN BONE-MARROW CULTURES WITH HEMATOPOIETIC GROWTH-FACTORS - IMPLICATIONS FOR SECONDARY LEUKEMIA POSTTRANSPLANT, Bone marrow transplantation, 19(5), 1997, pp. 521-523
A patient developed secondary acute myelogenous leukemia with a 20q- m
arker chromosome abnormality six years following chemotherapy and radi
ation for Hodgkins disease (HD). Routine cytogenetics on the bone marr
ow which had been harvested and cryopreserved immediately following co
mpletion of initial therapy for HD showed no cytogenetic abnormality.
However, a 20q- clonal marker was detected after culturing bone marrow
with hematopoietic growth factors (HGF). The marrow was used successf
ully for an autotransplant. Post-transplant, the 20q- marker was again
detected in HGF cultured samples. The patient relapsed at 165 days po
st-transplant with the 20q- marker and trisomy 21, These data suggest
that standard cytogenetic assays may not detect abnormal clones which
can cause leukemia post-transplant.