Cancers (Aug 2020)

Expression Patterns of Coagulation Factor XIII Subunit A on Leukemic Lymphoblasts Correlate with Clinical Outcome and Genetic Subtypes in Childhood B-cell Progenitor Acute Lymphoblastic Leukemia

  • Bettina Kárai,
  • Katalin Gyurina,
  • Anikó Ujfalusi,
  • Łukasz Sędek,
  • Gábor Barna,
  • Pál Jáksó,
  • Peter Svec,
  • Eszter Szánthó,
  • Attila Csaba Nagy,
  • Judit Müller,
  • Réka Simon,
  • Ágnes Vojczek,
  • István Szegedi,
  • Lilla Györgyi Tiszlavicz,
  • Jerzy R. Kowalczyk,
  • Alexandra Kolenova,
  • Gábor T. Kovács,
  • Tomasz Szczepański,
  • Michael Dworzak,
  • Angela Schumich,
  • Andishe Attarbaschi,
  • Karin Nebral,
  • Oskar A. Haas,
  • János Kappelmayer,
  • Zsuzsanna Hevessy,
  • Csongor Kiss

DOI
https://doi.org/10.3390/cancers12082264
Journal volume & issue
Vol. 12, no. 8
p. 2264

Abstract

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Background: Based on previous retrospective results, we investigated the association of coagulation FXIII subunit A (FXIII-A) expression pattern on survival and correlations with known prognostic factors of B-cell progenitor (BCP) childhood acute lymphoblastic leukemia (ALL) as a pilot study of the prospective multi-center BFM ALL-IC 2009 clinical trial. Methods: The study included four national centers (n = 408). Immunophenotyping by flow cytometry and cytogenetic analysis were performed by standard methods. Copy number alteration was studied in a subset of patients (n = 59). Survival rates were estimated by Kaplan-Meier analysis. Correlations between FXIII-A expression patterns and risk factors were investigated with Cox and logistic regression models. Results: Three different patterns of FXIII-A expression were observed: negative (<20%), dim (20–79%), and bright (≥80%). The FXIII-A dim expression group had significantly higher 5-year event-free survival (EFS) (93%) than the FXIII-A negative (70%) and FXIII-A bright (61%) groups. Distribution of intermediate genetic risk categories and the “B-other” genetic subgroup differed significantly between the FXIII-A positive and negative groups. Multivariate logistic regression confirmed independent association between the FXIII-A negative expression characteristics and the prevalence of intermediate genetic risk group. Conclusions: FXIII-A negativity is associated with dismal survival in children with BCP-ALL and is an indicator for the presence of unfavorable genetic alterations.

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