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MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy

High-risk neuroblastoma (HR-NB) includes MYCN-amplified stage 2/3, but reports covering anti-G(D2) immunotherapy, which recently became standard for HR-NB, do not provide details on this subset. We now report on all 20 MYCN-amplified stage 2/3 patients who received induction chemotherapy at our cent...

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Autores principales: Kushner, Brian H., LaQuaglia, Michael P., Modak, Shakeel, Wolden, Suzanne L., Basu, Ellen M., Roberts, Stephen S., Kramer, Kim, Yataghene, Karima, Cheung, Irene Y., Cheung, Nai-Kong V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707022/
https://www.ncbi.nlm.nih.gov/pubmed/29221128
http://dx.doi.org/10.18632/oncotarget.20513
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author Kushner, Brian H.
LaQuaglia, Michael P.
Modak, Shakeel
Wolden, Suzanne L.
Basu, Ellen M.
Roberts, Stephen S.
Kramer, Kim
Yataghene, Karima
Cheung, Irene Y.
Cheung, Nai-Kong V
author_facet Kushner, Brian H.
LaQuaglia, Michael P.
Modak, Shakeel
Wolden, Suzanne L.
Basu, Ellen M.
Roberts, Stephen S.
Kramer, Kim
Yataghene, Karima
Cheung, Irene Y.
Cheung, Nai-Kong V
author_sort Kushner, Brian H.
collection PubMed
description High-risk neuroblastoma (HR-NB) includes MYCN-amplified stage 2/3, but reports covering anti-G(D2) immunotherapy, which recently became standard for HR-NB, do not provide details on this subset. We now report on all 20 MYCN-amplified stage 2/3 patients who received induction chemotherapy at our center during the era of consolidation with anti-G(D2) antibody 3F8/ granulocyte-macrophage colony-stimulating factor (GM-CSF) (2000-2015). Early in this period, consolidation included autologous stem-cell transplantation (ASCT). Event-free survival (EFS) and overall survival (OS) were estimated using Kaplan-Meier analyses. With induction, 19/20 (95%) patients achieved complete/very good partial remission (CR/VGPR) but one had progressive disease with early death. One responder did not receive consolidation and died of relapse. Five-year post-diagnosis EFS/OS rates for all 20 patients were 72%/84%. The 18 CR/VGPR patients who received consolidation had EFS/OS 81%/94% at five years from starting 3F8/GM-CSF: 4/4 ASCT patients remained relapse-free, while 11/14 non-ASCT patients remained relapse-free and two of the three relapsed patients achieved 2(nd) CR (consolidated by retreatment with 3F8/GM-CSF) and remained in 2(nd) CR at 36+ and 95+ months post-relapse. The 14 non-ASCT patients had EFS/OS 73.5%/93% at five years from starting 3F8/GM-CSF. This subset appears to have a good prognosis with contemporary multi-modality therapy, possibly even without ASCT.
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spelling pubmed-57070222017-12-07 MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy Kushner, Brian H. LaQuaglia, Michael P. Modak, Shakeel Wolden, Suzanne L. Basu, Ellen M. Roberts, Stephen S. Kramer, Kim Yataghene, Karima Cheung, Irene Y. Cheung, Nai-Kong V Oncotarget Research Paper High-risk neuroblastoma (HR-NB) includes MYCN-amplified stage 2/3, but reports covering anti-G(D2) immunotherapy, which recently became standard for HR-NB, do not provide details on this subset. We now report on all 20 MYCN-amplified stage 2/3 patients who received induction chemotherapy at our center during the era of consolidation with anti-G(D2) antibody 3F8/ granulocyte-macrophage colony-stimulating factor (GM-CSF) (2000-2015). Early in this period, consolidation included autologous stem-cell transplantation (ASCT). Event-free survival (EFS) and overall survival (OS) were estimated using Kaplan-Meier analyses. With induction, 19/20 (95%) patients achieved complete/very good partial remission (CR/VGPR) but one had progressive disease with early death. One responder did not receive consolidation and died of relapse. Five-year post-diagnosis EFS/OS rates for all 20 patients were 72%/84%. The 18 CR/VGPR patients who received consolidation had EFS/OS 81%/94% at five years from starting 3F8/GM-CSF: 4/4 ASCT patients remained relapse-free, while 11/14 non-ASCT patients remained relapse-free and two of the three relapsed patients achieved 2(nd) CR (consolidated by retreatment with 3F8/GM-CSF) and remained in 2(nd) CR at 36+ and 95+ months post-relapse. The 14 non-ASCT patients had EFS/OS 73.5%/93% at five years from starting 3F8/GM-CSF. This subset appears to have a good prognosis with contemporary multi-modality therapy, possibly even without ASCT. Impact Journals LLC 2017-08-24 /pmc/articles/PMC5707022/ /pubmed/29221128 http://dx.doi.org/10.18632/oncotarget.20513 Text en Copyright: © 2017 Kushner et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Kushner, Brian H.
LaQuaglia, Michael P.
Modak, Shakeel
Wolden, Suzanne L.
Basu, Ellen M.
Roberts, Stephen S.
Kramer, Kim
Yataghene, Karima
Cheung, Irene Y.
Cheung, Nai-Kong V
MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy
title MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy
title_full MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy
title_fullStr MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy
title_full_unstemmed MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy
title_short MYCN-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-G(D2) immunotherapy
title_sort mycn-amplified stage 2/3 neuroblastoma: excellent survival in the era of anti-g(d2) immunotherapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5707022/
https://www.ncbi.nlm.nih.gov/pubmed/29221128
http://dx.doi.org/10.18632/oncotarget.20513
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