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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.
Kárai, Bettina; Gyurina, Katalin; Ujfalusi, Anikó; Sedek, Lukasz; Barna, Gábor; Jáksó, Pál; Svec, Peter; Szánthó, Eszter; Nagy, Attila Csaba; Müller, Judit; Simon, Réka; Vojczek, Ágnes; Szegedi, István; Tiszlavicz, Lilla Györgyi; Kowalczyk, Jerzy R; Kolenova, Alexandra; Kovács, Gábor T; Szczepanski, Tomasz; Dworzak, Michael; Schumich, Angela; Attarbaschi, Andishe; Nebral, Karin; Haas, Oskar A; Kappelmayer, János; Hevessy, Zsuzsanna; Kiss, Csongor.
Afiliação
  • Kárai B; Department of Laboratory of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
  • Gyurina K; Department of Pediatrics, University of Debrecen, 4032 Debrecen, Hungary.
  • Ujfalusi A; Department of Laboratory of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
  • Sedek L; Department of Microbiology and Immunology, Medical University of Silesia, 40-055 Katowice, Poland.
  • Barna G; 1st Department of Pathology and Experimental Cancer Research, Semmelweis University, 1085 Budapest, Hungary.
  • Jáksó P; Department of Pathology, Scientific University of Pécs, 7622 Pécs, Hungary.
  • Svec P; Department of Pediatric Hematology and Oncology, National Institute of Children's Diseases and Comenius University Bratislava, 833 40 Bratislava, Slovakia.
  • Szánthó E; Department of Laboratory of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
  • Nagy AC; Department of Preventive Medicine, Faculty of Public Health, University of Debrecen, 4028 Debrecen, Hungary.
  • Müller J; 2nd Department of Pediatrics, Semmelweis University, 1094 Budapest, Hungary.
  • Simon R; Department of Pediatric Hematology-Oncology, BAZ county university hospital pediatric center, 3526 Miskolc, Hungary.
  • Vojczek Á; Department of Pediatrics, Scientific University of Pécs, 7622 Pécs, Hungary.
  • Szegedi I; Department of Pediatrics, University of Debrecen, 4032 Debrecen, Hungary.
  • Tiszlavicz LG; Department of Pediatrics, Scientific University of Szeged, 6720 Szeged, Hungary.
  • Kowalczyk JR; Department of Pediatric Hematology, Oncology and Transplantology, Lublin Medical University, 20-059 Lublin, Poland.
  • Kolenova A; Department of Pediatric Hematology and Oncology, National Institute of Children's Diseases and Comenius University Bratislava, 833 40 Bratislava, Slovakia.
  • Kovács GT; 2nd Department of Pediatrics, Semmelweis University, 1094 Budapest, Hungary.
  • Szczepanski T; Department of Pediatric Hematology and Oncology, Medical University of Silesia Zabrze, 41-808 Zabrze, Poland.
  • Dworzak M; Children's Cancer Research Institute and St. Anna Children's Hospital, Pediatric Clinic, Medical University of Vienna, 1090 Vienna, Austria.
  • Schumich A; Children's Cancer Research Institute and St. Anna Children's Hospital, Pediatric Clinic, Medical University of Vienna, 1090 Vienna, Austria.
  • Attarbaschi A; Children's Cancer Research Institute and St. Anna Children's Hospital, Pediatric Clinic, Medical University of Vienna, 1090 Vienna, Austria.
  • Nebral K; Children's Cancer Research Institute and St. Anna Children's Hospital, Pediatric Clinic, Medical University of Vienna, 1090 Vienna, Austria.
  • Haas OA; Children's Cancer Research Institute and St. Anna Children's Hospital, Pediatric Clinic, Medical University of Vienna, 1090 Vienna, Austria.
  • Kappelmayer J; Department of Laboratory of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
  • Hevessy Z; Department of Laboratory of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
  • Kiss C; Department of Pediatrics, University of Debrecen, 4032 Debrecen, Hungary.
Cancers (Basel) ; 12(8)2020 Aug 13.
Article em En | MEDLINE | ID: mdl-32823516
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Ano de publicação: 2020 Tipo de documento: Article