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The prognostic value of IKZF1 in B-cell progenitor acute lymphoblastic leukemia: Results from the EORTC 58951 trial. | LitMetric

AI Article Synopsis

  • IKZF1 gene deletion is linked to poor prognosis in children with BCP-ALL, and additional genetic deletions like CDKN2A/2B or PAX5 can worsen outcomes further.
  • The study involved 1,200 patients with BCP-ALL, where those with IKZF1 deletions showed shorter event-free survival compared to those without, but differences between specific IKZF1 deletion groups were not significant.
  • Overall, the study concluded that while IKZF1 status indicates poor prognosis in BCP-ALL patients, adding more genetic factors did not significantly enhance its predictive value.

Article Abstract

Background: IKZF1 gene deletion is an indicator of poor prognosis in childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL). The AEIOP/BFM group proposed that the prognostic strength of IKZF1 deletion could be remarkably improved by taking into account additional genetic deletions and reported that among patients with an IKZF1 deletion those with deletions in CDKN2A/2B, PAX5, or PAR1 in the absence of ERG deletion, grouped as IKZF1 , had the worst outcome.

Procedure: Between 1998 and 2008, 1636 patients under 18 years of age with previously untreated BCP-ALL were registered in the EORTC 58951 trial. Those with multiplex ligation-dependent probe amplification data were included in this analysis. Unadjusted and adjusted Cox model was used to investigate the additional prognostic value of IKZF1 .

Results: Among 1200 patients included in the analysis, 1039 (87%) had no IKZF1 deletion (IKZF1 ), 87 (7%) had an IKZF1 deletion but not IKZF1 (IKZF1 ) and 74 (6%) had IKZF1 . In the unadjusted analysis, both patients with IKZF1 (hazard ratio [HR] = 2.10, 95% confidence interval [CI]: 1.34-3.31) and IKZF1 (HR = 3.07, 95% CI: 2.01-4.67) had a shorter event-free survival compared with IKZF1 . However, although the IKZF1 status was associated with patients' characteristics indicating poor prognosis, the difference between IKZF1 and IKZF1 was not statistically significant (HR = 1.46, 95% CI: 0.83-2.57, p = .19). The results of the adjusted analysis were similar to the unadjusted analysis.

Conclusions: In patients with BCP-ALL from the EORTC 58951 trial, the improvement of the prognostic importance of IKZF1 by considering IKZF1 was not statistically significant.

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Source
http://dx.doi.org/10.1002/pbc.30313DOI Listing

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