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Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma

BACKGROUND: Allogeneic stem cell transplantation (allo-SCT) and donor lymphocyte infusions (DLI) may induce a graft-versus-tumor effect in pediatric sarcoma patients. Here, we describe general feasibility, toxicity and efficacy of DLI after allo-SCT. RESULTS: 4 of 8 patients responded. ES#4 had stab...

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Autores principales: Schober, Sebastian J., von Luettichau, Irene, Wawer, Angela, Steinhauser, Maximilian, Salat, Christoph, Schwinger, Wolfgang, Ussowicz, Marek, Antunovic, Petar, Castagna, Luca, Kolb, Hans-Jochem, Burdach, Stefan E.G., Thiel, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978262/
https://www.ncbi.nlm.nih.gov/pubmed/29854312
http://dx.doi.org/10.18632/oncotarget.25228
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author Schober, Sebastian J.
von Luettichau, Irene
Wawer, Angela
Steinhauser, Maximilian
Salat, Christoph
Schwinger, Wolfgang
Ussowicz, Marek
Antunovic, Petar
Castagna, Luca
Kolb, Hans-Jochem
Burdach, Stefan E.G.
Thiel, Uwe
author_facet Schober, Sebastian J.
von Luettichau, Irene
Wawer, Angela
Steinhauser, Maximilian
Salat, Christoph
Schwinger, Wolfgang
Ussowicz, Marek
Antunovic, Petar
Castagna, Luca
Kolb, Hans-Jochem
Burdach, Stefan E.G.
Thiel, Uwe
author_sort Schober, Sebastian J.
collection PubMed
description BACKGROUND: Allogeneic stem cell transplantation (allo-SCT) and donor lymphocyte infusions (DLI) may induce a graft-versus-tumor effect in pediatric sarcoma patients. Here, we describe general feasibility, toxicity and efficacy of DLI after allo-SCT. RESULTS: 4 of 8 patients responded. ES#4 had stable disease (SD) for 9 months after DLI and RMS#4 partial response for 8 months with combined hyperthermia/chemotherapy. In ES#4, DLI led to SD for 6 months and reverted residual disease before allo-SCT into complete remission. After DLI, ES#4 and RMS#4 developed acute GvHD (°III–°IV), ES#4 also developed chronic GvHD. 5 patients including ES#4 lived longer than expected. Median survival after allo-SCT was 2.3 years, post-relapse survival (PRS) was 13 months. Off note, HLA-mismatched DLI were associated with a trend towards increased survival after allo-SCT and increased PRS compared to HLA-matched DLI (23 versus 3 months). MATERIALS AND METHODS: We studied eight adolescents and young adults (AYAs) with advanced Ewing sarcoma (ES#1-4) and rhabdomyosarcoma (RMS#1-4) who received DLI. Escalating doses ranged from 2.5 × 10(4) to 1 × 10(8) CD3(+) cells/kg body weight. AYAs were evaluated for response to DLI, graft-versus-host disease (GvHD) and survival. CONCLUSIONS: DLI after allo-SCT may control advanced pediatric sarcoma in AYAs with controllable toxicity.
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spelling pubmed-59782622018-05-31 Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma Schober, Sebastian J. von Luettichau, Irene Wawer, Angela Steinhauser, Maximilian Salat, Christoph Schwinger, Wolfgang Ussowicz, Marek Antunovic, Petar Castagna, Luca Kolb, Hans-Jochem Burdach, Stefan E.G. Thiel, Uwe Oncotarget Research Paper BACKGROUND: Allogeneic stem cell transplantation (allo-SCT) and donor lymphocyte infusions (DLI) may induce a graft-versus-tumor effect in pediatric sarcoma patients. Here, we describe general feasibility, toxicity and efficacy of DLI after allo-SCT. RESULTS: 4 of 8 patients responded. ES#4 had stable disease (SD) for 9 months after DLI and RMS#4 partial response for 8 months with combined hyperthermia/chemotherapy. In ES#4, DLI led to SD for 6 months and reverted residual disease before allo-SCT into complete remission. After DLI, ES#4 and RMS#4 developed acute GvHD (°III–°IV), ES#4 also developed chronic GvHD. 5 patients including ES#4 lived longer than expected. Median survival after allo-SCT was 2.3 years, post-relapse survival (PRS) was 13 months. Off note, HLA-mismatched DLI were associated with a trend towards increased survival after allo-SCT and increased PRS compared to HLA-matched DLI (23 versus 3 months). MATERIALS AND METHODS: We studied eight adolescents and young adults (AYAs) with advanced Ewing sarcoma (ES#1-4) and rhabdomyosarcoma (RMS#1-4) who received DLI. Escalating doses ranged from 2.5 × 10(4) to 1 × 10(8) CD3(+) cells/kg body weight. AYAs were evaluated for response to DLI, graft-versus-host disease (GvHD) and survival. CONCLUSIONS: DLI after allo-SCT may control advanced pediatric sarcoma in AYAs with controllable toxicity. Impact Journals LLC 2018-04-27 /pmc/articles/PMC5978262/ /pubmed/29854312 http://dx.doi.org/10.18632/oncotarget.25228 Text en Copyright: © 2018 Schober et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Schober, Sebastian J.
von Luettichau, Irene
Wawer, Angela
Steinhauser, Maximilian
Salat, Christoph
Schwinger, Wolfgang
Ussowicz, Marek
Antunovic, Petar
Castagna, Luca
Kolb, Hans-Jochem
Burdach, Stefan E.G.
Thiel, Uwe
Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
title Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
title_full Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
title_fullStr Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
title_full_unstemmed Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
title_short Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
title_sort donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978262/
https://www.ncbi.nlm.nih.gov/pubmed/29854312
http://dx.doi.org/10.18632/oncotarget.25228
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