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Mian, M.; Rinaldi, A.; Mensah, A.A.; Rossi, D.; Ladetto, M.; Forconi, F.; Marasca, R.; Uhr, M.; Stussi, G.; Kwee, I.; Cavalli, F.; Gaidano, G.; Zucca, E.; Bertoni, F.
Annals of oncology, 05/2013, Letnik: 24, Številka: 5Journal Article
Genomic complexity can predict the clinical course of patients affected by chronic lymphocytic leukemia (CLL) with a normal FISH. However, large studies are still lacking. Here, we analyzed a large series of CLL patients and also carried out the so far largest comparison of FISH versus single-nucleotide polymorphism (SNP) array in this disease. SNP-array data were derived from a previously reported dataset. Seventy-seven of 329 CLL patients (23%) presented with a normal FISH. At least one large (>5 Mb) genomic aberration was detected by SNP array in 17 of 77 patients (22%); this finding significantly affected TTT. There was no correlation with the presence of TP53 mutations. In multivariate analysis, including age, Binet stage, IGHV genes mutational status and large genomic lesion, the latter three factors emerged as independent prognosticators. The concordance between FISH and SNP array varied between 84 and 97%, depending on the specific genomic locus investigated. SNP array detected additional large genomic aberrations not covered by the standard FISH panel predicting the outcome of CLL patients.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Vir: Osebne bibliografije
in: SICRIS
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