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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.

Authors :
Kárai B
Gyurina K
Ujfalusi A
Sędek Ł
Barna G
Jáksó P
Svec P
Szánthó E
Nagy AC
Müller J
Simon R
Vojczek Á
Szegedi I
Tiszlavicz LG
Kowalczyk JR
Kolenova A
Kovács GT
Szczepański T
Dworzak M
Schumich A
Attarbaschi A
Nebral K
Haas OA
Kappelmayer J
Hevessy Z
Kiss C
Source :
Cancers [Cancers (Basel)] 2020 Aug 13; Vol. 12 (8). Date of Electronic Publication: 2020 Aug 13.
Publication Year :
2020

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.<br />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.<br />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.<br />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.

Details

Language :
English
ISSN :
2072-6694
Volume :
12
Issue :
8
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
32823516
Full Text :
https://doi.org/10.3390/cancers12082264