Deletion analysis of p16INKa and p15INKb in relapsed childhood acute lymphoblastic leukemia

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Abstract

This study aimed at determining the prevalence of INK4 deletions and their impact on outcome in 125 children with acute lymphoblastic leukemia (ALL) at first relapse using real-time quantitative polymerase chain reaction. Patients were enrolled into relapse trials ALL-REZ BFM (ALL-Relapse Berlin-Frankfurt-Münster) 90 and 96. The prevalence of p16INK4a and p15INK4b homozygous deletions was 35% (44 of 125) and 30% (38 of 125), respectively. A highly significant association of both gene deletions was found with the 2 major adverse prognostic factors known for relapsed childhood ALL: T-cell immunophenotype and first remission duration. There was no correlation between INK4 deletions and probability of event-free survival. These findings argue against an independent prognostic role of INK4 deletions in relapsed childhood ALL. © 2002 by The American Society of Hematology.

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Einsiedel, H. G., Taube, T., Hartmann, R., Wellmann, S., Seifert, G., Henze, G., & Seeger, K. (2002). Deletion analysis of p16INKa and p15INKb in relapsed childhood acute lymphoblastic leukemia. Blood, 99(12), 4629–4631. https://doi.org/10.1182/blood.V99.12.4629

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