DNA copy number alterations mark disease progression in paediatric chronic myeloid leukaemia

Summary Early recognition of children with chronic phase chronic myeloid leukaemia (CML‐CP) at risk for developing a lymphoid blast crisis (LyBC) is desirable, because therapy options in CML‐LyBC are limited. We used Multiplex Ligation‐dependent Probe Amplification to determine whether B‐cell lympho...

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Veröffentlicht in:British journal of haematology 2014-07, Vol.166 (2), p.250-253
Hauptverfasser: Sligte, Naomi E., Krumbholz, Manuela, Pastorczak, Agata, Scheijen, Blanca, Tauer, Josephine T., Nowasz, Christina, Sonneveld, Edwin, Bock, Geertruida H., Meeuwsen‐de Boer, Tiny G. J., Reijmersdal, Simon, Kuiper, Roland P., Bradtke, Jutta, Metzler, Markus, Suttorp, Meinolf, Bont, Evelina S. J. M., Leeuwen, Frank N.
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Sprache:eng
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Zusammenfassung:Summary Early recognition of children with chronic phase chronic myeloid leukaemia (CML‐CP) at risk for developing a lymphoid blast crisis (LyBC) is desirable, because therapy options in CML‐LyBC are limited. We used Multiplex Ligation‐dependent Probe Amplification to determine whether B‐cell lymphoid leukaemia‐specific copy number alterations (CNAs) (e.g. IKZF1, PAX5, CDKN2A deletions) could be detected in CML‐CP and may be used to predict disease progression to LyBC. CNAs were detected in all patients with CML‐LyBC, but in none of the 77 patients with CML‐CP. Based on this study we conclude that CNAs remain a hallmark of disease progression.
ISSN:0007-1048
1365-2141
DOI:10.1111/bjh.12850