Abstract:
:The (1;19)(q23;p13) translocation, leading to the production of the E2A/PBX1 fusion transcript, is one of the most common translocations in pediatric B-lineage acute lymphoblastic leukemia (ALL). It was assumed to be associated with a poor clinical outcome, although intensive therapy and bone marrow transplantation have been shown to be able to overcome the negative prognostic impact. Only few data are available concerning t(1;19)(q23;p13) in adult ALL. In particular, the prognostic significance of this genetic aberration is not yet clear. We describe three cases of adult ALL carrying the t(1;19)(q23;p13), who were all characterized by an aggressive clinical course and short survival, and discuss the molecular features of the disease as recently identified by gene expression profiling.
journal_name
Leuk Lymphomajournal_title
Leukemia & lymphomaauthors
Piccaluga PP,Malagola M,Rondoni M,Ottaviani E,Testoni N,Laterza C,Visani G,Pileri SA,Martinelli G,Baccarani Mdoi
10.1080/10428190500331261keywords:
subject
Has Abstractpub_date
2006-03-01 00:00:00pages
469-72issue
3eissn
1042-8194issn
1029-2403pii
L56842M70V3870L1journal_volume
47pub_type
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