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

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Veröffentlicht in:Cancers 2021-04, Vol.13 (9), p.2075
Hauptverfasser: 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, Felix, Csoka, Monika, Krivan, Gergely, Palma, Julia, Burke, G A Amos, Beishuizen, Auke, Koeppen, Kristin, Mueller, Stephanie, Herbrueggen, Heidi, Woessmann, Wilhelm, Zimmermann, Martin, Balduzzi, Adriana, Pillon, Marta
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container_end_page
container_issue 9
container_start_page 2075
container_title Cancers
container_volume 13
creator 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, Felix
Csoka, Monika
Krivan, Gergely
Palma, Julia
Burke, G A Amos
Beishuizen, Auke
Koeppen, Kristin
Mueller, Stephanie
Herbrueggen, Heidi
Woessmann, Wilhelm
Zimmermann, Martin
Balduzzi, Adriana
Pillon, Marta
description 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.
doi_str_mv 10.3390/cancers13092075
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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 &lt; 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.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13092075</identifier><identifier>PMID: 33923026</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adolescents ; Anaplastic large-cell lymphoma ; B-cell lymphoma ; Bone marrow ; Burkitt's lymphoma ; Children ; Clinical trials ; Diagnosis ; Hematopoietic stem cells ; Immune system ; Leukemia ; Lymphocytes B ; Lymphoma ; Non-Hodgkin's lymphoma ; Patients ; Risk factors ; Stem cell transplantation ; Teenagers</subject><ispartof>Cancers, 2021-04, Vol.13 (9), p.2075</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. 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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 &lt; 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. 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Shing</au><au>Bubanska, Eva</au><au>Donska, Svetlana</au><au>Hjalgrim, Lisa Lyngsie</au><au>Wachowiak, Jacek</au><au>Pieczonka, Anna</au><au>Uyttebroeck, Anne</au><au>Lazic, Jelena</au><au>Loeffen, Jan</au><au>Buechner, Jochen</au><au>Niggli, Felix</au><au>Csoka, Monika</au><au>Krivan, Gergely</au><au>Palma, Julia</au><au>Burke, G A Amos</au><au>Beishuizen, Auke</au><au>Koeppen, Kristin</au><au>Mueller, Stephanie</au><au>Herbrueggen, Heidi</au><au>Woessmann, Wilhelm</au><au>Zimmermann, Martin</au><au>Balduzzi, Adriana</au><au>Pillon, Marta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment and Outcome Analysis of 639 Relapsed Non-Hodgkin Lymphomas in Children and Adolescents and Resulting Treatment Recommendations</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2021-04-25</date><risdate>2021</risdate><volume>13</volume><issue>9</issue><spage>2075</spage><pages>2075-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><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 &lt; 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.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>33923026</pmid><doi>10.3390/cancers13092075</doi><orcidid>https://orcid.org/0000-0002-7107-618X</orcidid><orcidid>https://orcid.org/0000-0003-4853-4354</orcidid><orcidid>https://orcid.org/0000-0002-5879-0610</orcidid><orcidid>https://orcid.org/0000-0002-1151-829X</orcidid><orcidid>https://orcid.org/0000-0001-5644-424X</orcidid><orcidid>https://orcid.org/0000-0003-2671-9972</orcidid><orcidid>https://orcid.org/0000-0001-5536-6788</orcidid><orcidid>https://orcid.org/0000-0002-1089-5325</orcidid><orcidid>https://orcid.org/0000-0002-4680-603X</orcidid><orcidid>https://orcid.org/0000-0002-9285-6898</orcidid><orcidid>https://orcid.org/0000-0001-5848-4501</orcidid><orcidid>https://orcid.org/0000-0002-1559-8223</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 2072-6694
ispartof Cancers, 2021-04, Vol.13 (9), p.2075
issn 2072-6694
2072-6694
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8123268
source MDPI - Multidisciplinary Digital Publishing Institute; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
subjects Adolescents
Anaplastic large-cell lymphoma
B-cell lymphoma
Bone marrow
Burkitt's lymphoma
Children
Clinical trials
Diagnosis
Hematopoietic stem cells
Immune system
Leukemia
Lymphocytes B
Lymphoma
Non-Hodgkin's lymphoma
Patients
Risk factors
Stem cell transplantation
Teenagers
title Treatment and Outcome Analysis of 639 Relapsed Non-Hodgkin Lymphomas in Children and Adolescents and Resulting Treatment Recommendations
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