Abstract
Acute lymphoblastic leukaemia (ALL) remains a leading cause of non-traumatic death in children, and the majority of adults diagnosed will succumb to the disease. Recent advances in molecular biology and bioinformatics have enabled more detailed genomic analysis and a better understanding of the molecular biology of ALL. A number of recurrent genomic drivers have recently been described, which not only aid in diagnosis and prognostication, but also may offer opportunities for specific therapeutic targeting. The present review summarises B-ALL genomic pathology at diagnosis, including lesions detectable using traditional cytogenetic methods as well as those detected only through advanced molecular techniques.
Original language | English |
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Pages (from-to) | 13-27 |
Number of pages | 15 |
Journal | British Journal of Haematology |
Volume | 197 |
Issue number | 1 |
DOIs | |
Publication status | Published or Issued - Apr 2022 |
Keywords
- acute lymphoblastic leukaemia (ALL)
- acute lymphoblastic leukaemia diagnosis
- acute lymphoblastic leukaemia genomics
- acute lymphoblastic leukaemia prognostication
- molecular pathology
ASJC Scopus subject areas
- Hematology