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dc.contributor.author Burkhardt, B
dc.contributor.author Taj, M
dc.contributor.author Garnier, N
dc.contributor.author Minard-Colin, V
dc.contributor.author Hazar, V
dc.contributor.author Mellgren, K
dc.contributor.author Osumi, T
dc.contributor.author Fedorova, A
dc.contributor.author Myakova, N
dc.contributor.author Verdu-Amoros, J
dc.contributor.author Andres, M
dc.contributor.author Kabickova, E
dc.contributor.author Attarbaschi, A
dc.contributor.author Chiang, AKS
dc.contributor.author Bubanska, E
dc.contributor.author Donska, S
dc.contributor.author Hjalgrim, LL
dc.contributor.author Wachowiak, J
dc.contributor.author Pieczonka, A
dc.contributor.author Uyttebroeck, A
dc.contributor.author Lazic, J
dc.contributor.author Loeffen, J
dc.contributor.author Buechner, J
dc.contributor.author Niggli, F
dc.contributor.author Csóka, Monika
dc.contributor.author Kriván, Gergely
dc.contributor.author Palma, J
dc.contributor.author Amos, Burke GA
dc.contributor.author Beishuizen, A
dc.contributor.author Koeppen, K
dc.contributor.author Mueller, S
dc.contributor.author Herbrueggen, H
dc.contributor.author Woessmann, W
dc.contributor.author Zimmermann, M
dc.contributor.author Balduzzi, A
dc.contributor.author Pillon, M
dc.date.accessioned 2022-03-07T08:19:51Z
dc.date.available 2022-03-07T08:19:51Z
dc.date.issued 2021
dc.identifier 85104606116
dc.identifier.citation journalVolume=13;journalIssueNumber=9;pagination=2075, pages: 18;journalTitle=CANCERS;journalAbbreviatedTitle=CANCERS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8995
dc.identifier.uri doi:10.3390/cancers13092075
dc.description.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. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
dc.relation.ispartof urn:issn:2072-6694
dc.title Treatment and outcome analysis of 639 relapsed non-hodgkin lymphomas in children and adolescents and resulting treatment recommendations
dc.type Journal Article
dc.date.updated 2022-01-06T19:24:52Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 31997765
dc.identifier.wos 000649881100001
dc.identifier.pubmed 33923026
dc.contributor.department SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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