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Results and conclusions of the European Intergroup EURO-LB02 trial in children and adolescents with lymphoblastic lymphoma.
Landmann, Eva; Burkhardt, Birgit; Zimmermann, Martin; Meyer, Ulrike; Woessmann, Wilhelm; Klapper, Wolfram; Wrobel, Grazyna; Rosolen, Angelo; Pillon, Marta; Escherich, Gabriele; Attarbaschi, Andishe; Beishuizen, Auke; Mellgren, Karin; Wynn, Robert; Ratei, Richard; Plesa, Adriana; Schrappe, Martin; Reiter, Alfred; Bergeron, Christophe; Patte, Catherine; Bertrand, Yves.
Afiliação
  • Landmann E; Department of Pediatric Hematology and Oncology, Justus-Liebig-University, Giessen, Germany.
  • Burkhardt B; Department of Pediatric Hematology and Oncology, Children's University Hospital, Münster, Germany birgit.burkhardt@ukmuenster.de.
  • Zimmermann M; Department of Pediatric Hematology and Oncology, Hannover Medical School, Germany.
  • Meyer U; Department of Pediatric Hematology and Oncology, Justus-Liebig-University, Giessen, Germany.
  • Woessmann W; Department of Pediatric Hematology and Oncology, Justus-Liebig-University, Giessen, Germany.
  • Klapper W; Department of Hematopathology and Lymph Node Registry, University Hospital, Kiel, Germany.
  • Wrobel G; Department of Bone Marrow Transplantation, Children's Oncology and Hematology, Wroclaw Medical University, Poland.
  • Rosolen A; Clinica di Oncoematologia Pediatrica, Università di Padova, Italy.
  • Pillon M; Clinica di Oncoematologia Pediatrica, Università di Padova, Italy.
  • Escherich G; Clinic for Pediatric Hematology and Oncology, University Medical Center, Hamburg, Germany.
  • Attarbaschi A; Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Austria.
  • Beishuizen A; Department of Pediatric Hematology/Oncology, Erasmus MC - Sophia Children's Hospital, Rotterdam, the Netherlands and the Dutch Childhood Oncology Group, the Hague, the Netherlands.
  • Mellgren K; Department of Pediatric Oncology and Hematology, The Queen Silvia Children's Hospital, Göteborg, Sweden.
  • Wynn R; Central Manchester University Hospitals, Great Britain.
  • Ratei R; Department of Hematology, Oncology and Tumor Immunology, Helios Klinikum, Berlin-Buch, Germany.
  • Plesa A; Department of Hematopathology and Flow Cytometry, CHU, Lyon-HCL, France.
  • Schrappe M; Department of Pediatrics, Christian-Albrechts-University, Kiel, Germany.
  • Reiter A; Department of Pediatric Hematology and Oncology, Justus-Liebig-University, Giessen, Germany.
  • Bergeron C; Institut d'Hematologie et d'Oncologie Pediatrique, Centre Léon Bérard and HCL, Claude Bernard University, Lyon, France.
  • Patte C; Department of Gustave Roussy, Villejuif, France.
  • Bertrand Y; Institut d'Hematologie et d'Oncologie Pediatrique, Centre Léon Bérard and HCL, Claude Bernard University, Lyon, France.
Haematologica ; 102(12): 2086-2096, 2017 12.
Article em En | MEDLINE | ID: mdl-28983060
In the European Intergroup EURO-LB02 trial, children and adolescents with lymphoblastic lymphoma underwent the non-Hodgkin lymphoma Berlin-Frankfurt-Münster protocol without prophylactic cranial radiotherapy. The primary aims of this trial were to test whether replacing prednisone with dexamethasone during induction increases event-free survival in the subgroups with T-cell lymphoblastic lymphoma and whether therapy duration could be reduced from 24 to 18 months (factorial design, randomizations). These questions could not be answered due to premature closure of the trial. Here we report on the secondary aims of the trial: whether the results of the NHL-BFM90 study could be reproduced and evaluation of disease features and prognostic factors. Three hundred and nineteen patients (66 with precursor B-cell lymphoblastic lymphoma, 233 with T-cell lymphoblastic lymphoma, 12 with mixed phenotype, 8 not classifiable) were enrolled. In induction, 215 patients received prednisone and 104 patients received dexamethasone. The median follow-up was 6.8 years (range, 3.0-10.3). The 5-year event-free survival was 82±2% [12 toxic deaths, 5 secondary malignancies, 43 non-response/relapse (central nervous system n=9; all received prednisone during induction)]. The event-free survival rate was 80±5% for patients with precursor B-cell lymphoblastic lymphoma, 82±3% for those with T-cell lymphoblastic lymphoma, and 100% for patients with a mixed phenotype. During induction, significantly more grade III/IV toxicities were observed in patients receiving dexamethasone, resulting in significant treatment delays. The number of toxic deaths did not differ significantly. The only variable associated with outcome was performance status at diagnosis. The 90% event-free survival rate for patients with T-cell lymphoblastic lymphoma shown in study NHL-BFM90 was not replicated, mainly due to more toxic deaths and central nervous system relapses. Dexamethasone in induction may prevent central nervous system relapse more effectively than prednisone but produces a higher burden of toxicity. (#NCT00275106).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: Haematologica Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Europa Idioma: En Revista: Haematologica Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Alemanha