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Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma
The impact of bone marrow (BM) GD2-positive cells on survival has been evaluated in 145 Italian children with localised neuroblastoma (NB) evaluated at diagnosis by anti-GD2 immunocytochemistry. Nineteen of these (13.1%) were found to be BM GD2-positive, with the number of positive cells ranging bet...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361437/ https://www.ncbi.nlm.nih.gov/pubmed/18182983 http://dx.doi.org/10.1038/sj.bjc.6604179 |
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author | Corrias, M V Parodi, S Haupt, R Lacitignola, L Negri, F Sementa, A R Dau, D Scuderi, F Carlini, B Bianchi, M Casale, F Faulkner, L Garaventa, A |
author_facet | Corrias, M V Parodi, S Haupt, R Lacitignola, L Negri, F Sementa, A R Dau, D Scuderi, F Carlini, B Bianchi, M Casale, F Faulkner, L Garaventa, A |
author_sort | Corrias, M V |
collection | PubMed |
description | The impact of bone marrow (BM) GD2-positive cells on survival has been evaluated in 145 Italian children with localised neuroblastoma (NB) evaluated at diagnosis by anti-GD2 immunocytochemistry. Nineteen of these (13.1%) were found to be BM GD2-positive, with the number of positive cells ranging between 1 and 155 out of 1 × 10(6) total cells analysed. Seven/19 (38.8%) GD2-positive vs 12/126 (9.5%) GD2-negative patients relapsed. The 5-year event-free survival (EFS) and overall survival of the GD2-positive patients was significantly worse than that of the GD2-negative ones (62.2 vs 89.9%, P<0.001; and 74.9 vs 95.9%, P=0.005, respectively). GD2 positivity was not associated to other known risk factors, and in particular to Myc-N amplification and 1p deletion. Among Myc-N-negative patients, the EFS of those negative for both GD2 and 1p deletion was significantly better than in children positive for either one of these two markers (EFS=96.9 vs 66.0%, P<0.001). In conclusion, GD2 positivity may represent a prognostic marker for patients with non-metastatic NB without Myc-N amplification, and its combination with genetic alterations might help identifying patients that require a more careful follow-up. |
format | Text |
id | pubmed-2361437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23614372009-09-10 Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma Corrias, M V Parodi, S Haupt, R Lacitignola, L Negri, F Sementa, A R Dau, D Scuderi, F Carlini, B Bianchi, M Casale, F Faulkner, L Garaventa, A Br J Cancer Clinical Study The impact of bone marrow (BM) GD2-positive cells on survival has been evaluated in 145 Italian children with localised neuroblastoma (NB) evaluated at diagnosis by anti-GD2 immunocytochemistry. Nineteen of these (13.1%) were found to be BM GD2-positive, with the number of positive cells ranging between 1 and 155 out of 1 × 10(6) total cells analysed. Seven/19 (38.8%) GD2-positive vs 12/126 (9.5%) GD2-negative patients relapsed. The 5-year event-free survival (EFS) and overall survival of the GD2-positive patients was significantly worse than that of the GD2-negative ones (62.2 vs 89.9%, P<0.001; and 74.9 vs 95.9%, P=0.005, respectively). GD2 positivity was not associated to other known risk factors, and in particular to Myc-N amplification and 1p deletion. Among Myc-N-negative patients, the EFS of those negative for both GD2 and 1p deletion was significantly better than in children positive for either one of these two markers (EFS=96.9 vs 66.0%, P<0.001). In conclusion, GD2 positivity may represent a prognostic marker for patients with non-metastatic NB without Myc-N amplification, and its combination with genetic alterations might help identifying patients that require a more careful follow-up. Nature Publishing Group 2008-01-29 2008-01-08 /pmc/articles/PMC2361437/ /pubmed/18182983 http://dx.doi.org/10.1038/sj.bjc.6604179 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Corrias, M V Parodi, S Haupt, R Lacitignola, L Negri, F Sementa, A R Dau, D Scuderi, F Carlini, B Bianchi, M Casale, F Faulkner, L Garaventa, A Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
title | Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
title_full | Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
title_fullStr | Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
title_full_unstemmed | Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
title_short | Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
title_sort | detection of gd2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361437/ https://www.ncbi.nlm.nih.gov/pubmed/18182983 http://dx.doi.org/10.1038/sj.bjc.6604179 |
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