SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3

• Published in: Genes chromosomes & cancer 2012-08, Vol.51 (8), p.756-767
• Main Authors: Nowak, Daniel, Klaumuenzer, Marion, Hanfstein, Benjamin, Mossner, Maximilian, Nolte, Florian, Nowak, Verena, Oblaender, Julia, Hecht, Anna, Hütter, Gero, Ogawa, Seishi, Kohlmann, Alexander, Haferlach, Claudia, Schlegelberger, Brigitte, Braess, Jan, Seifarth, Wolfgang, Fabarius, Alice, Erben, Philipp, Saussele, Susanne, Müller, Martin C., Reiter, Andreas, Buechner, Thomas, Weiss, Christel, Hofmann, Wolf-Karsten, Lengfelder, Eva
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Aged, 80 and over; Biomarkers, Tumor; Child; Chromosome Aberrations; Chromosomes, Human, Pair 1; DNA Copy Number Variations; Female; Gene Deletion; Humans; Kaplan-Meier Estimate; Leukemia, Promyelocytic, Acute - genetics; Loss of Heterozygosity; Male; Middle Aged; Oligonucleotide Array Sequence Analysis; Oncogene Proteins, Fusion - genetics; Polymorphism, Single Nucleotide; Reproducibility of Results; Risk Factors; Statistics, Nonparametric; Translocation, Genetic
• ISSN: 1045-2257; 1098-2264
• DOI: 10.1002/gcc.21961

To search for new copy number alterations (CNAs) in acute promyelocytic leukemia (APL), we analyzed DNA from leukemic blasts of 93 acute promyelocytic leukemia (APL) patients with Genome‐Wide SNP 6.0 arrays (SNP‐A). We identified 259 CNAs consisting of 170 heterozygous deletions, 82 amplifications, and 7 regions of copy number neutral loss of heterozygosity. One of the most common CNAs was a deletion on chromosomal subband 1q31.3 in 13 of 93 (14%) patients encompassing the coding regions for the microRNAs mir181a1/b1. In multivariable analysis with the covariates age, white blood cell count, platelet count, and FLT3‐ITD/FLT3 D835 mutations we found that after adjustment for patients' age (P < 0.0001), patients with 2 or more CNAs detected by SNP‐A had a higher risk of death (hazard ratio = 5.942, P = 0.0015) than patients with 0 or 1 CNA. Deletions of 1q31.3 were associated with a higher number of CNAs (median 2 vs. 8, P < 0.0001) and were a strong independent prognostic factor for an increased risk of relapse (hazard ratio = 28.9, P = 0.0031). This study presents a comprehensive assessment of new CNAs as pathomechanistically relevant targets and possible prognostic factors which could refine risk stratification of APL. © 2012 Wiley Periodicals, Inc.