IKZF1 alterations predict poor prognosis in adult and pediatric T-ALL
Author(s) -
Mathieu Simonin,
Ludovic Lhermitte,
Marie-Émilie Dourthe,
Étienne Lengliné,
Carlos Graux,
Nathalie Grardel,
JeanMichel Cayuela,
Isabelle Arnoux,
Virginie Gandemer,
Norbert Ifrah,
Hervé Dombret,
André Baruchel,
Elizabeth Macintyre,
Arnaud Petit,
Nicolas Boissel,
Vahid Asnafi
Publication year - 2020
Publication title -
blood
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.515
H-Index - 465
eISSN - 1528-0020
pISSN - 0006-4971
DOI - 10.1182/blood.2020007959
Subject(s) - minimal residual disease , oncology , lymphoblastic leukemia , multivariate analysis , medicine , immunology , leukemia
Patient outcomes in T-cell acute lymphoblastic leukemia and lymphoblastic lymphoma (T-ALL/LBL) can be difficult to predict. Simonin et al report deletions and mutations in the gene encoding the transcription factor IKAROS among 1260 children and adults with immature T-ALL/LBL, defining its frequency and, importantly, its association with poor outcome in multivariate models. Pathogenic alterations in IKZF1 now can be added to minimal residual disease detection and the established 4-gene oncogenetic classifier to better predict poor outcomes of T-ALL/LBL.
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