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Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study
BACKGROUND: We conducted a retrospective analysis to investigate treatment results and prognostic factors of pediatric neuroblastoma patients. METHODS: This retrospective study was carried out analyzing the medical records of patients with the pathological diagnosis of neuroblastoma seen at South Eg...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018370/ https://www.ncbi.nlm.nih.gov/pubmed/21182799 http://dx.doi.org/10.1186/1755-7682-3-37 |
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author | El-Sayed, Mohamed I Ali, Amany M Sayed, Heba A Zaky, Eman M |
author_facet | El-Sayed, Mohamed I Ali, Amany M Sayed, Heba A Zaky, Eman M |
author_sort | El-Sayed, Mohamed I |
collection | PubMed |
description | BACKGROUND: We conducted a retrospective analysis to investigate treatment results and prognostic factors of pediatric neuroblastoma patients. METHODS: This retrospective study was carried out analyzing the medical records of patients with the pathological diagnosis of neuroblastoma seen at South Egypt Cancer Institute, Assiut University during the period from January 2001 and January 2010. After induction chemotherapy, response according to international neuoblastoma response criteria was assessed. Radiotherapy to patients with residual primary tumor was applied. Overall and event free survival (OAS and EFS) rates were estimated using Graphed prism program. The Log-rank test was used to examine differences in OAS and EFS rates. Cox-regression multivariate analysis was done to determine the independent prognostic factors affecting survival rates. RESULTS: Fifty three cases were analyzed. The median follow-up duration was 32 months and ranged from 2 to 84 months. The 3-year OAS and EFS rates were 39.4% and 29.3% respectively. Poor prognostic factors included age >1 year of age, N-MYC amplification, and high risk group. The majority of patients (68%) presented in high risk group, where treatment outcome was poor, as only 21% of patients survived for 3 year. CONCLUSION: Multivariate analysis confirmed only the association between survival and risk group. However, in univariate analysis, local radiation therapy resulted in significant survival improvement. Therefore, radiotherapy should be given to patients with residual tumor evident after induction chemotherapy and surgery. Future attempts to improve OAS in high risk group patients with aggressive chemotherapy and bone marrow transplantation should be considered. |
format | Text |
id | pubmed-3018370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30183702011-01-11 Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study El-Sayed, Mohamed I Ali, Amany M Sayed, Heba A Zaky, Eman M Int Arch Med Original Research BACKGROUND: We conducted a retrospective analysis to investigate treatment results and prognostic factors of pediatric neuroblastoma patients. METHODS: This retrospective study was carried out analyzing the medical records of patients with the pathological diagnosis of neuroblastoma seen at South Egypt Cancer Institute, Assiut University during the period from January 2001 and January 2010. After induction chemotherapy, response according to international neuoblastoma response criteria was assessed. Radiotherapy to patients with residual primary tumor was applied. Overall and event free survival (OAS and EFS) rates were estimated using Graphed prism program. The Log-rank test was used to examine differences in OAS and EFS rates. Cox-regression multivariate analysis was done to determine the independent prognostic factors affecting survival rates. RESULTS: Fifty three cases were analyzed. The median follow-up duration was 32 months and ranged from 2 to 84 months. The 3-year OAS and EFS rates were 39.4% and 29.3% respectively. Poor prognostic factors included age >1 year of age, N-MYC amplification, and high risk group. The majority of patients (68%) presented in high risk group, where treatment outcome was poor, as only 21% of patients survived for 3 year. CONCLUSION: Multivariate analysis confirmed only the association between survival and risk group. However, in univariate analysis, local radiation therapy resulted in significant survival improvement. Therefore, radiotherapy should be given to patients with residual tumor evident after induction chemotherapy and surgery. Future attempts to improve OAS in high risk group patients with aggressive chemotherapy and bone marrow transplantation should be considered. BioMed Central 2010-12-24 /pmc/articles/PMC3018370/ /pubmed/21182799 http://dx.doi.org/10.1186/1755-7682-3-37 Text en Copyright ©2010 El-Sayed et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research El-Sayed, Mohamed I Ali, Amany M Sayed, Heba A Zaky, Eman M Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
title | Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
title_full | Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
title_fullStr | Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
title_full_unstemmed | Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
title_short | Treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
title_sort | treatment results and prognostic factors of pediatric neuroblastoma: a retrospective study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018370/ https://www.ncbi.nlm.nih.gov/pubmed/21182799 http://dx.doi.org/10.1186/1755-7682-3-37 |
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