Treatment and outcome analysis of 639 relapsed non-hodgkin lymphomas in children and adolescents and resulting treatment recommendations
Artículo
Open/ Download
Access note
Acceso abierto
Publication date
2021Metadata
Show full item record
Cómo citar
Burkhardt, Birgit
Cómo citar
Treatment and outcome analysis of 639 relapsed non-hodgkin lymphomas in children and adolescents and resulting treatment recommendations
Author
- Burkhardt, Birgit;
- Taj, Mary;
- Garnier, Nathalie;
- Minard Colin, Veronique;
- Hazar, Volkan;
- Mellgren, Karin;
- Osumi, Tomoo;
- Fedorova, Alina;
- Myakova, Natalia;
- Verdu Amoros, Jaime;
- Andres, Mara;
- Kabickova, Edita;
- Attarbaschi, Andishe;
- Chiang, Alan Kwok Shing;
- Bubanska, Eva;
- Donska, Svetlana;
- Hjalgrim, Lisa Lyngsie;
- Wachowiak, Jacek;
- Pieczonka, Anna;
- Uyttebroeck, Anne;
- Lazic, Jelena;
- Loeffen, Jan;
- Buechner, Jochen;
- Niggli, Félix;
- Csoka, Monika;
- Krivan, Gergely;
- Palma Behnke, Julia Irene;
- Burke, G. A. Amos;
- Beishuizen, Auke;
- Koeppen, Kristin;
- Mueller, Stephanie;
- Herbrueggen, Heidi;
- Woessmann, Wilhelm;
- Zimmermann, Martin;
- Balduzzi, Adriana;
- Pillon, Marta;
Abstract
Simple Summary: Despite very poor survival, controversies remain in the treatment for refractory
or relapsed non-Hodgkin lymphoma (r/r NHL) in children and adolescents. The current project identifies
and reports international experience on re-induction treatment of r/r NHL, hematopoietic stem
cell transplantation, risk factors associated with outcome, and suggests treatment recommendations.
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.
Patrocinador
Deutsche Kinderkrebsstiftung DKS 2014.11A/B
DKS 2016.24A/B
Indexation
Artículo de publícación WoS
Quote Item
Cancers 2021, 13, 2075
Collections
The following license files are associated with this item: