Klin Padiatr 2019; 231(03): 164
DOI: 10.1055/s-0039-1687155
Abstracts
Georg Thieme Verlag KG Stuttgart · New York

FOS and FOSB are linked with CNS-infiltration and inferior prognosis in childhood T-cell acute lymphoblastic leukemia

Authors

  • L Spory

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany

  • L Lenk

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany

  • D Winterberg

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany

  • A Alsadeq

    2   Institute of Immunology, Ulm University Medical Center, Ulm, Germany

  • M Carlet

    3   Helmholtz Zentrum München, Department of Gene Vectors, Research Center for Environmental Health, Munich, Germany

  • I Jeremias

    3   Helmholtz Zentrum München, Department of Gene Vectors, Research Center for Environmental Health, Munich, Germany

  • G Cario

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany

  • M Schrappe

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany

  • M Vossen-Gajcy

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany

  • DM Schewe

    1   Department of Pediatrics I, Pediatric Hematology/Oncology, ALL-BFM Study Group, University Medical Center Schleswig-Holstein, Kiel, Germany
Further Information

Publication History

Publication Date:
20 May 2019 (online)

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    Aim:

    CNS involvement in ALL is a major clinical challenge, particularly in T-ALL. Novel targets to reliably detect and eradicate CNS-leukemia are urgently needed.

    Methods:

    Comparative RNA-sequencing was performed with patient derived xenograft TALL blasts recovered from the bone marrow (BM) and the CNS of NSG-mice. FOS and FOSB mRNA were measured in diagnostic bone marrow samples of 112 pediatric T-ALL patients and correlated with clinical parameters.

    Results:

    The AP-1 genes FOS and FOSB were significantly upregulated in blasts recovered from the CNS versus BM of NSG-mice. Accordingly, CNS+ patients exposed significantly elevated FOSB-mRNA levels as compared to CNS- patients (p = 0.038). Furthermore, FOShigh and FOSBhigh patients (mRNA levels above median) showed significantly lower 5-year event free survival (p = 0.031 and p = 0.011, respectively) than FOSlow and FOSBlow patients. Importantly, 6/9 patients with CNS-relapse were FOShigh and FOSBhigh upon diagnosis.

    Conclusion:

    FOS and FOSB may be novel independent predictors of prognosis and surrogate markers with therapeutic potential for CNS-infiltration and relapse in T-ALL requiring further prospective and mechanistic validation.