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

Author:

Kárai Bettina,Gyurina Katalin,Ujfalusi Anikó,Sędek Łukasz,Barna Gábor,Jáksó PálORCID,Svec PeterORCID,Szánthó Eszter,Nagy Attila Csaba,Müller Judit,Simon Réka,Vojczek Ágnes,Szegedi István,Tiszlavicz Lilla Györgyi,Kowalczyk Jerzy R.ORCID,Kolenova AlexandraORCID,Kovács Gábor T.ORCID,Szczepański TomaszORCID,Dworzak Michael,Schumich Angela,Attarbaschi AndisheORCID,Nebral Karin,Haas Oskar A.ORCID,Kappelmayer János,Hevessy ZsuzsannaORCID,Kiss CsongorORCID

Abstract

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.

Funder

Hungarian Science Foundation

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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