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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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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. |
format | Online Article Text |
id | pubmed-5707022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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