Cytogenetic analysis is useful in the diagnosis and to assess prognosis of
B-cell chronic lymphocytic leukemia (B-CLL). However, successful cytogeneti
cs by standard techniques has been hindered by the low in vitro mitotic act
ivity of the malignant B-cell population. Fluorescence in situ hybridizatio
n (FISH) has become a useful tool, but it does not provide an overall view
of the aberrations. To overcome this hurdle, two DNA-based techniques have
been tested in the present study: comparative genomic hybridization (CGH) a
nd amplotyping by arbitrarily primed PCR (AP-PCR). Comparative genomic hybr
idization resolution depends upon the 400-bands of the human standard karyo
type. AP-PCR allows detection of allelic losses and gains in tumor cells by
PCR fingerprinting, thus its resolution is at the molecular level. Both te
chniques were performed in 23 patients with stage A B-CLL at diagnosis. The
results were compared with FISH. The sensitivity of AP-PCR was greater tha
n CGH (62% vs 43%). The use of CGH combined with AP-PCR allowed to detect g
enetic abnormalities in 79% (15/19) of patients in whom G-banding wa,, not
informative. providing a global view of the aberrations in a sole experimen
t. This study shows that combining these two methods with FISH, makes possi
ble a more precise genetic characterization of patients with B-CLL. (C) 200
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