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Treatment and Outcome Analysis of 639 Relapsed Non-Hodgkin Lymphomas in Children and Adolescents and Resulting Treatment Recommendations
B. Burkhardt, M. Taj, N. Garnier, V. Minard-Colin, V. Hazar, K. Mellgren, T. Osumi, A. Fedorova, N. Myakova, J. Verdu-Amoros, M. Andres, E. Kabickova, A. Attarbaschi, AKS. Chiang, E. Bubanska, S. Donska, LL. Hjalgrim, J. Wachowiak, A. Pieczonka,...
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
DKS 2014.11A/B, DKS 2016.24A/B
Deutsche Kinderkrebsstiftung
NLK
Free Medical Journals
od 2009
PubMed Central
od 2009
Europe PubMed Central
od 2009
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Open Access Digital Library
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2009
PubMed
33923026
DOI
10.3390/cancers13092075
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
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.
2nd Department of Pediatrics Semmelweis University 1085 Budapest Hungary
Children's Cancer Centre National Centre for Child Health and Development Tokyo 104 0045 Japan
Department of Pediatric Hematology and Oncology Oslo University Hospital 0424 Oslo Norway
Department of Pediatric Hematology and Oncology University Hospital Valencia 46010 Valencia Spain
Department of Pediatric Oncology Royal Marsden Hospital Surrey SM2 5PT UK
Department of Pediatric Oncology University Children's Hospital Zurich 8032 Zürich Switzerland
Department of Pediatric Oncology University Hospital Le Fe 46026 Valencia Spain
Department of Pediatrics and Adolescent Medicine 2100 Copenhagen Denmark
Hannover Medical School Department of Pediatric Hematology and Oncology 30625 Hannover Germany
Hospices Civils de Lyon Institute of Pediatric Hematology and Oncology 69002 Lyon France
National Research Centre for Pediatric Hematology Oncology and Immunology 129090 Moscow Russia
Pediatric Hematology and Oncology University Medical Centre Hamburg Eppendorf 20246 Hamburg Germany
Princess Máxima Centre for Pediatric Oncology 3584 CS Utrecht The Netherlands
Citace poskytuje Crossref.org
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