Treatment and Outcome Analysis of 639 Relapsed Non-Hodgkin Lymphomas in Children and Adolescents and Resulting Treatment Recommendations

Birgit Burkhardt(University Hospital Münster), Mary Taj(Royal Marsden Hospital), Nathalie Garnier(Hospices Civils de Lyon), Véronique Minard‐Colin(Université Paris-Saclay), Volkan Hazar(Antalya IVF), Karin Mellgren(Sahlgrenska University Hospital), Tomoo Osumi, Alina Fedorova(Belarusian Research Center For Pediatric Oncology and Hematology), N. V. Myakova, Jaime Verdú‐Amorós(Hospital Clínico Universitario de Valencia), Mara Andrés(Hospital Universitari i Politècnic La Fe), Edita Kabíčková(Charles University), Andishe Attarbaschi(St Anna Children's Hospital), Aks Chiang(Queen Mary Hospital), Eva Bubanská, S. Donska, Lisa Lyngsie Hjalgrim, Jacek Wachowiak(Poznan University of Medical Sciences), Anna Pieczonka(Poznan University of Medical Sciences), Anne Uyttebroeck(KU Leuven), Jelena Lazić(University of Belgrade), Jan Loeffen(Princess Máxima Center), Jochen Buechner(Oslo University Hospital), Felix Niggli(University Children's Hospital Zurich), Monika Csóka(Semmelweis University), Gergely Kriván(National Center for Epidemiology), Julia Palma(Hospital Luis Calvo Mackenna), G.A. Amos Burke(Cambridge University Hospitals NHS Foundation Trust), Auke Beishuizen(Princess Máxima Center), Kristin Koeppen(University Hospital Münster), Stephanie Mueller(University Hospital Münster), Heidi Herbrueggen(University Hospital Münster), Wilhelm Woessmann(Universität Hamburg), Martin Zimmermann(Medizinische Hochschule Hannover), Adriana Balduzzi(University of Milano-Bicocca), Marta Pillon(University of Padua)
Cancers
April 25, 2021
Cited by 46Open Access
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Abstract

Despite poor survival, controversies remain in the treatment for refractory or relapsed pediatric non-Hodgkin lymphoma (r/r NHL). The current project aimed to collect international experience on the re-induction treatment of r/r NHL, hematopoietic stem cell transplantation (HSCT), risk factors associated with outcome, and to suggest treatment recommendations. Inclusion criteria were (i) refractory disease, disease progression or relapse of any NHL subtype except anaplastic large cell lymphoma, (ii) age < 18 years at initial diagnosis, (iii) diagnosis in/after January 2000. Data from 639 eligible patients were evaluable. The eight-year probability of overall survival was 34 ± 2% with highly significant differences according to NHL subtypes: 28 ± 3% for 254 Burkitt lymphoma/leukemia, 50 ± 6% for 98 diffuse large B-cell lymphomas, 57 ± 8% for 41 primary mediastinal large B-cell lymphomas, 27 ± 3% for 177 T-lymphoblastic lymphomas, 52 ± 10% for 34 precursor-B-cell lymphoblastic lymphomas and 30 ± 9% for 35 patients with rare NHL subtypes. Subtype-specific factors associated with survival and treatment recommendations are suggested. There were no survivors without HSCT, except in few very small subgroups. Conclusions: There is an urgent need to further improve survival in r/r NHL. The current study provides the largest real-world series, which underlines the role of HSCT and suggests treatment recommendations.


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