Analysis of CD34 populations in mobilised peripheral blood stem cell harvests and in bone marrow by fluorescent in situ hybridisation for the bcr ablgene fusion in patients with chronic granulocytic leukaemia
Jae. Irving et al., Analysis of CD34 populations in mobilised peripheral blood stem cell harvests and in bone marrow by fluorescent in situ hybridisation for the bcr ablgene fusion in patients with chronic granulocytic leukaemia, LEUKEMIA, 13(6), 1999, pp. 944-949
For those patients ineligible for allogeneic bone marrow transplant and who
are non-responsive to interferon, autotransplant with peripheral blood ste
m cells (PBSC) mobilised after intensive chemotherapy, may provide a novel
approach to improve prognosis in patients with chronic granulocytic leukaem
ia. PBSC harvests are assessed for CD84-positive cell numbers, which serve
as an indicator of engraftment potential, and are also analysed cytogenetic
ally to ascertain tumour cell contamination. However, a more accurate asses
sment of PBSC harvest contamination requires investigation of the Philadelp
hia (Ph) status of the CD34(pos) population, in which the cells that provid
e long-term engraftment are contained. In this study, we have analysed thes
e levels in mobilised PBSC and also in bone marrow (BM) harvests, taken sev
eral weeks prior to mobilising chemotherapy. Using fluorescent in situ hybr
idisation for the bcr/abl gene fusion, we have shown that the median number
of Ph negative cells in CD34(pos) isolated populations was 14.95% in BM co
mpared to 79.05% in PBSC harvests and that in all PBSC samples tested, Ph p
ositivity in CD34(pos) populations was always detectable either by FISH or
one round PCR methods. In paired assessments of both PBSC and BM harvests,
higher levels of Ph negative CD34(pos) cells (greater than or equal to 14%)
isolated from BM harvests, taken prior to intensive chemotherapy, correlat
ed with higher levels of Ph negative CD34(pos) cells (greater than or equal
to 78.5%) in PBSC harvests. These data may aid in the selection of patient
s for whom PBSC harvesting, after mobilisation, is more likely to achieve a
n autograft product containing predominantly Ph negative CD34(pos) cells an
d may exclude those patients for whom the risk, morbidity and expense of st
em cell harvesting may have no apparent benefit over a chronic phase BM har
vest.