TY - JOUR
T1 - Treatment and Outcome Analysis of 639 Relapsed Non-Hodgkin Lymphomas in Children and Adolescents and Resulting Treatment Recommendations
AU - Burkhardt, Birgit
AU - Taj, Mary
AU - Garnier, Nathalie
AU - Minard-Colin, Veronique
AU - Hazar, Volkan
AU - Mellgren, Karin
AU - Osumi, Tomoo
AU - Fedorova, Alina
AU - Myakova, Natalia
AU - Verdu-Amoros, Jaime
AU - Andres, Mara
AU - Kabickova, Edita
AU - Attarbaschi, Andishe
AU - Chiang, Alan Kwok Shing
AU - Bubanska, Eva
AU - Donska, Svetlana
AU - Hjalgrim, Lisa Lyngsie
AU - Wachowiak, Jacek
AU - Pieczonka, Anna
AU - Uyttebroeck, Anne
AU - Lazic, Jelena
AU - Loeffen, Jan
AU - Buechner, Jochen
AU - Niggli, Felix
AU - Csoka, Monika
AU - Krivan, Gergely
AU - Palma, Julia
AU - Burke, G A Amos
AU - Beishuizen, Auke
AU - Koeppen, Kristin
AU - Mueller, Stephanie
AU - Herbrueggen, Heidi
AU - Woessmann, Wilhelm
AU - Zimmermann, Martin
AU - Balduzzi, Adriana
AU - Pillon, Marta
PY - 2021/4/25
Y1 - 2021/4/25
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85104606116&partnerID=8YFLogxK
U2 - 10.3390/cancers13092075
DO - 10.3390/cancers13092075
M3 - Journal article
C2 - 33923026
SN - 2072-6694
VL - 13
JO - Cancers
JF - Cancers
IS - 9
M1 - 2075
ER -