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Different outcome of T cell acute lymphoblastic leukemia with translocation t(11;14) treated in two consecutive children leukemia group EORTC trials

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Abstract

Acute lymphoblastic leukemia of T cell lineage (T-ALL) is an aggressive malignant disease which accounts for 15 % of childhood ALL. T(11;14) is the more frequent chromosomal abnormality in childhood T-ALL, but its prognostic value remained controversial. Our aim was to analyze the outcome of childhood T-ALL with t(11;14) to know if the presence of this translocation is associated with a poor prognosis. We conducted a retrospective study from a series of 20 patients with t(11;14), treated in two consecutive trials from the European Organization for Research and Treatment of Cancer Children Leukemia Group over a 19-year period from 1989 to 2008. There were no significant differences between the 2 consecutive groups of patients with t(11;14) regarding the clinical and biological features at diagnosis. Among 19 patients who reached complete remission, 9 patients relapsed. We noticed 7 deaths all relapse- or failure-related. In the 58881 study, a presence of t(11;14) was associated with a poor outcome with an event-free survival at 5 years at 22.2 % versus 65.1 % for the non-t(11;14) T-ALL (p = 0.0004). In the more recent protocol, the outcome of T-ALL with t(11;14) reached that of non-t(11;14) T-ALL with an event-free survival at 5 years at 65.5 versus 74.9 % (p = 0.93). The presence of t(11;14) appeared as a poor prognostic feature in the 58881 trial whereas this abnormality no longer affected the outcome in the 58951 study. This difference is probably explained by the more intensive chemotherapy in the latest trial.

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Acknowledgments

The authors would like to thank the EORTC-CLG study group members for their participation in the study; a complete list of the participating institutions and investigators appears in the Appendix. The authors would like to thank the EORTC HQ Data Management Department members (Séraphine Rosse, Lies Meirlaen, Liv Meert, Aurélie Dubois, Christine Waterkeyn, Alessandra Busato, Isabel VandeVelde, and Gabriel Solbu) for their support of this trial. This study was supported by the EORTC Charitable Trust Foundation; Vlaamse Liga Tegen Kanker, Belgian Federation Against Cancer, non-profit organization; and TéléVie and Kinderkankerfonds from Belgium.

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Correspondence to Pierre S. Rohrlich.

Ethics declarations

Informed consent was provided according to the Declaration of Helsinki. These protocols have been accepted by the EORTC Protocol Review Committee and by the ethics committee of each participating center.

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The authors declare that they have no conflict of interest.

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Appendix

Appendix

Information about the contributions of each person named as having participated in the study

  1. 1.

    Guarantor(s), i.e., person(s) who is (are) responsible for the integrity of the work as a whole:

    • Pauline Simon, Department of Pediatric Hematology-Oncology, CHU, Besançon, France; p1simon@chu-besancon.fr

    • Pierre S Rohrlich, Department of Pediatric Hematology-Oncology, CHU, Nice, France; rohrlich.ps@chu-nice.fr

    • Nicole Dastugue, Laboratory of Cytogenetics, University Hospital, Toulouse, France

    • Stefan Suciu, EORTC Headquarters, Brussels, Belgium, stefan.suciu@eortc.be

    The guarantors of this manuscript confirm that all persons designated as authors qualify for authorship and that each author has participated sufficiently in the work to take public responsibility for appropriate portions of the content.

  2. 2.

    Authors who participated in the conception of the study: Pauline SIMON, Pierre S Rohrlich, Stefan Suciu, and Nicole Dastugue

  3. 3.

    Design and methods. The following authors were responsible for specific investigations:

    • Yves Bertrand, Yves Benoit, Stefan Suciu, and Hélène Cavé developed the study design.

    • Nicolas Sirvent, Geneviève Plat, Antoine Thyss, Françoise Mechinaud, Vitor M Costa, Alina Ferster, Patrick Lutz, Françoise Mazingue, Dominique Plantaz, Emmanuel Plouvier, Yves Bertrand, Yves Benoit, and Pierre S Rohrlich were involved in the acquisition of clinical data.

    • Emmanuelle Clappier and Hélène Cave were responsible for molecular data.

    • Nicole Dastugue was responsible for the cytogenetics.

    • Stefan Suciu developed the analytical approach to the data.

  4. 4.

    Results. The following authors were responsible for specific portions of the results, including figures and tables:

    • Pauline Simon, Pierre S. Rohrlich, and Stefan Suciu were involved in the analysis and/or interpretation of data.

    • Stefan Suciu performed the statistical analyses.

    • Pauline Simon, Pierre S. Rohrlich, Stefan Suciu, and Nicole Dastugue prepared and are responsible for all figures and tables.

  5. 5.

    Writing the manuscript. The following authors were responsible for writing the manuscript:

    • Pauline Simon, Pierre S. Rohrlich, and Nicole Dastugue drafted the manuscript.

    • Emmanuelle Clappier, Hélène Cavé, Alina Ferster, Yves Bertrand, Yves Benoit, and Nicole Dastugue critically evaluated the manuscript and actively improved its scientific value.

    • Stefan Suciu, Emmanuelle Clappier, Hélène Cavé, Nicolas Sirvent, Geneviève Plat, Antoine Thyss, Françoise Mechinaud, Vitor M. Costa, Alina Ferster, Patrick Lutz, Françoise Mazingue, Dominique Plantaz, Emmanuel Plouvier, Yves Bertrand, Yves Benoit, and Nicole Dastugue approved the final version of the manuscript.

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Simon, P., Suciu, S., Clappier, E. et al. Different outcome of T cell acute lymphoblastic leukemia with translocation t(11;14) treated in two consecutive children leukemia group EORTC trials. Ann Hematol 95, 93–103 (2016). https://doi.org/10.1007/s00277-015-2515-8

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  • DOI: https://doi.org/10.1007/s00277-015-2515-8

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