Abstract
Background. WT1 is aberrantly over-expressed in most cases of AML. We recently demonstrated that WT1 SNP rs16754 correlates with favorable outcome and high diagnostic WT1 expression in childhood AML. We examined the clinical correlates of diagnostic WT1 expression within a contemporary COG trial and determined whether its prognostic impact differs between SNP+ and SNP- patients. Procedure. WT1 mRNA expression was measured via qRTPCR in diagnostic specimens obtained from 225 patients enrolled on COG-AAML03P1. Direct sequencing of WT1 exon 7 was performed to determine SNP rs16754 genotype. WT1 expression was correlated with disease characteristics, SNP status, and outcome. Results. Patients were categorized into four groups (quartiles:Q1 through Q4) based on diagnostic WT1 expression for analysis. FLT3/ITD (P=0.017) and WT1 mutations (P<0.001) both occurred more frequently in patients with the highest WT1 expression. SNP rs16754 frequency did not vary significantly among the quartiles. When all patients were considered, survival outcomes were similar between quartiles. However, when only SNP- patients (n=150) were analyzed, those with highest WT1 expression (Q4) had the poorest OS (51% vs. 72% for Q1-Q3, P=0.006) and EFS (35% vs. 54% for Q1-Q3, P=0.031). Among SNP+ patients (n=75), survival did not vary significantly between WT1 expression quartiles. Conclusion. Although WT1 expression was not prognostic when all patients were considered together, stratifying patients by SNP rs16754 genotype revealed significant differences in outcome. In SNP- patients, high WT1 expression predicted decreased survival in univariate, but not multivariate, analysis, due to a preponderance of high-risk cyto/molecular abnormalities in the highest expression quartile. Pediatr Blood Cancer 2014;61:81-88.
Original language | English (US) |
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Pages (from-to) | 81-88 |
Number of pages | 8 |
Journal | Pediatric Blood and Cancer |
Volume | 61 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2014 |
Bibliographical note
Publisher Copyright:© 2013 Wiley Periodicals, Inc.
Keywords
- AML
- Molecular diagnosis and therapy
- Prognostic factors
- Rs16754
- WT1