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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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 < 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. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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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 < 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><subject>Adolescents</subject><subject>Anaplastic large-cell lymphoma</subject><subject>B-cell lymphoma</subject><subject>Bone marrow</subject><subject>Burkitt's lymphoma</subject><subject>Children</subject><subject>Clinical trials</subject><subject>Diagnosis</subject><subject>Hematopoietic stem cells</subject><subject>Immune system</subject><subject>Leukemia</subject><subject>Lymphocytes B</subject><subject>Lymphoma</subject><subject>Non-Hodgkin's lymphoma</subject><subject>Patients</subject><subject>Risk factors</subject><subject>Stem cell 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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 < 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> |
fulltext | fulltext |
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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