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Frequency and clinical impact of CDKN2A/ARF/CDKN2B gene deletions as assessed by in-depth genetic analyses in adult T cell acute lymphoblastic leukemia.

Authors :
Genescà E
Lazarenkov A
Morgades M
Berbis G
Ruíz-Xivillé N
Gómez-Marzo P
Ribera J
Juncà J
González-Pérez A
Mercadal S
Guardia R
Artola MT
Moreno MJ
Martínez-López J
Zamora L
Barba P
Gil C
Tormo M
Cladera A
Novo A
Pratcorona M
Nomdedeu J
González-Campos J
Almeida M
Cervera J
Montesinos P
Batlle M
Vives S
Esteve J
Feliu E
Solé F
Orfao A
Ribera JM
Source :
Journal of hematology & oncology [J Hematol Oncol] 2018 Jul 24; Vol. 11 (1), pp. 96. Date of Electronic Publication: 2018 Jul 24.
Publication Year :
2018

Abstract

Recurrent deletions of the CDKN2A/ARF/CDKN2B genes encoded at chromosome 9p21 have been described in both pediatric and adult acute lymphoblastic leukemia (ALL), but their prognostic value remains controversial, with limited data on adult T-ALL. Here, we investigated the presence of homozygous and heterozygous deletions of the CDKN2A/ARF and CDKN2B genes in 64 adult T-ALL patients enrolled in two consecutive trials from the Spanish PETHEMA group. Alterations in CDKN2A/ARF/CDKN2B were detected in 35/64 patients (55%). Most of them consisted of 9p21 losses involving homozygous deletions of the CDKNA/ARF gene (26/64), as confirmed by single nucleotide polymorphism (SNP) arrays and interphase fluorescence in situ hybridization (iFISH). Deletions involving the CDKN2A/ARF/CDKN2B locus correlated with a higher frequency of cortical T cell phenotype and a better clearance of minimal residual disease (MRD) after induction therapy. Moreover, the combination of an altered copy-number-value (CNV) involving the CDKN2A/ARF/CDKN2B gene locus and undetectable MRD (≤ 0.01%) values allowed the identification of a subset of T-ALL with better overall survival in the absence of hematopoietic stem cell transplantation.

Details

Language :
English
ISSN :
1756-8722
Volume :
11
Issue :
1
Database :
MEDLINE
Journal :
Journal of hematology & oncology
Publication Type :
Report
Accession number :
30041662
Full Text :
https://doi.org/10.1186/s13045-018-0639-8