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12th Congress of the European Hematology ... - Haematologica

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induced significant apoptosis (mean value 32±12%), colony growth<br />

reduction (mean value <strong>of</strong> 34,2 vs 76,5) and proliferation rate inhibition<br />

(48%±17) in EphA3+ cells compared to normal controls and to EphA3<br />

negative cells in which we were unable to observed any significant effect.<br />

Similar effects were observed after incubation with a specific antibody<br />

blocking <strong>the</strong> receptor. No kinase domain mutations were found in EphA3<br />

overexpressing cells. Conclusions. EphA3 is abnormally expressed in different<br />

hematological malignancies with a significant overexpression in<br />

CMPD as compared to normal controls. The inhibition <strong>of</strong> EphA3 phosphorylation<br />

induced by Dasatinib or by <strong>the</strong> antibody results in growth<br />

arrest and apoptosis <strong>of</strong> EphA3 overexpressing cells. Therefore, EphA3<br />

may represent a potential candidate for a molecular <strong>the</strong>rapy in chronic<br />

myeloproliferative disorders<br />

0666<br />

AUTOMATED FISH ANALYSIS PREDICTS GOOD OUTCOME IN CML PATIENTS WITH<br />

IMATINIB-INDUCED REMISSION AND DETECTS VERY LOW LEVEL LEUKAEMIC CELL<br />

POPULATION WITH DOUBLE BCR-ABL REARRANGEMENT<br />

G. Calabrese, 1 R. Di Lorenzo, 2 S. Pulini, 2 D. Fantasia, 3 P. Guanciali-<br />

Franchi, 1 R. Di Gianfilippo, 3 D. Romagno, 3 M. Alfonsi, 1 G. Fioritoni, 2<br />

G. Palka1 1 Medical Genetic, University <strong>of</strong> Chieti, CHIETI; 2 Department <strong>of</strong> <strong>Hematology</strong>,<br />

PESCARA; 3 Human Genetic, PESCARA, Italy<br />

Background.Minimal residual disease (MRD) analysis is essential for<br />

establishing <strong>the</strong> efficacy <strong>of</strong> <strong>the</strong>rapy in chronic myeloid leukemia (CML)<br />

patients. Aims. Seventy-six patients with CML, 69 in chronic phase, 1<br />

in accelerate phase, and 6 in blastic crisis, were treated with imatinib<br />

mesylate (IM). We used automated FISH analysis to evaluate <strong>the</strong> MRD<br />

as a predictor <strong>of</strong> efficacy <strong>of</strong> IM <strong>the</strong>rapy. Methods. The patients were<br />

studied for a 18-66 months follow up period using cytogenetics and<br />

FISH analysis with a dual-fusion BCR-ABL probe, and an automated<br />

FISH imaging system for rare cell events (BioView-Duet). Before IM<br />

treatment 50 patients showed Ph chromosome in all examined cells<br />

while in <strong>the</strong> remaining 26 patients a normal clone was also found.<br />

Results. Complete or partial cytogenetic remission rate [CCR or PCR:<br />

t(9;22) absent or

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