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The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience

AIM OF THE STUDY: Neuroblastoma (NBL) is one of the most common extracranial tumours occurring in children with N-Myc gene amplification, acknowledged as a marker of poor prognosis. We assessed the frequency of N-Myc amplification and its impact on NBL markers and on the treatment outcome. MATERIAL...

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Autores principales: Kaczówka, Przemysław, Wieczorek, Aleksandra, Czogała, Małgorzata, Książek, Teofila, Szewczyk, Katarzyna, Balwierz, Walentyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377415/
https://www.ncbi.nlm.nih.gov/pubmed/30783385
http://dx.doi.org/10.5114/wo.2018.81402
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author Kaczówka, Przemysław
Wieczorek, Aleksandra
Czogała, Małgorzata
Książek, Teofila
Szewczyk, Katarzyna
Balwierz, Walentyna
author_facet Kaczówka, Przemysław
Wieczorek, Aleksandra
Czogała, Małgorzata
Książek, Teofila
Szewczyk, Katarzyna
Balwierz, Walentyna
author_sort Kaczówka, Przemysław
collection PubMed
description AIM OF THE STUDY: Neuroblastoma (NBL) is one of the most common extracranial tumours occurring in children with N-Myc gene amplification, acknowledged as a marker of poor prognosis. We assessed the frequency of N-Myc amplification and its impact on NBL markers and on the treatment outcome. MATERIAL AND METHODS: Among 160 children with NBL treated from 1991 to 2015 in one centre 140 patients had known N-Myc gene status, and they were enrolled in the study. The analysed group was divided into two subgroups: with and without N-Myc amplification (25 and 115 children, respectively). Association of N-Myc amplification with stage of the disease, levels of biochemical parameters, overall survival (OS) and failure-free survival (FFS) were analysed. RESULTS: The frequency of N-Myc amplification was 17.9%. Most children with N-Myc amplification (64%) were classified to stage 4 NBL. The levels of biochemical markers of NBL: ferritin, dopamine, NSE, and LDH were significantly higher in the group with N-Myc amplification, whereas the levels of VMA and HVA were lower. OS and FFS were significantly lower in children with N-Myc amplification in comparison to children from the control group (OS 53% vs. 76%, p = 0.03; FFS 50% vs. 72%, p = 0.03). The impact of N-Myc amplification on the treatment outcome was significant in patients with stage 4 NBL and children under one year of age. CONCLUSIONS: N-Myc amplification is a crucial prognostic factor in neuroblastoma, which is associated with almost all features related with poor prognosis and a higher probability of unfavourable outcome.
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spelling pubmed-63774152019-02-19 The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience Kaczówka, Przemysław Wieczorek, Aleksandra Czogała, Małgorzata Książek, Teofila Szewczyk, Katarzyna Balwierz, Walentyna Contemp Oncol (Pozn) Original Paper AIM OF THE STUDY: Neuroblastoma (NBL) is one of the most common extracranial tumours occurring in children with N-Myc gene amplification, acknowledged as a marker of poor prognosis. We assessed the frequency of N-Myc amplification and its impact on NBL markers and on the treatment outcome. MATERIAL AND METHODS: Among 160 children with NBL treated from 1991 to 2015 in one centre 140 patients had known N-Myc gene status, and they were enrolled in the study. The analysed group was divided into two subgroups: with and without N-Myc amplification (25 and 115 children, respectively). Association of N-Myc amplification with stage of the disease, levels of biochemical parameters, overall survival (OS) and failure-free survival (FFS) were analysed. RESULTS: The frequency of N-Myc amplification was 17.9%. Most children with N-Myc amplification (64%) were classified to stage 4 NBL. The levels of biochemical markers of NBL: ferritin, dopamine, NSE, and LDH were significantly higher in the group with N-Myc amplification, whereas the levels of VMA and HVA were lower. OS and FFS were significantly lower in children with N-Myc amplification in comparison to children from the control group (OS 53% vs. 76%, p = 0.03; FFS 50% vs. 72%, p = 0.03). The impact of N-Myc amplification on the treatment outcome was significant in patients with stage 4 NBL and children under one year of age. CONCLUSIONS: N-Myc amplification is a crucial prognostic factor in neuroblastoma, which is associated with almost all features related with poor prognosis and a higher probability of unfavourable outcome. Termedia Publishing House 2018-12-31 2018 /pmc/articles/PMC6377415/ /pubmed/30783385 http://dx.doi.org/10.5114/wo.2018.81402 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Kaczówka, Przemysław
Wieczorek, Aleksandra
Czogała, Małgorzata
Książek, Teofila
Szewczyk, Katarzyna
Balwierz, Walentyna
The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience
title The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience
title_full The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience
title_fullStr The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience
title_full_unstemmed The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience
title_short The role of N-Myc gene amplification in neuroblastoma childhood tumour – single-centre experience
title_sort role of n-myc gene amplification in neuroblastoma childhood tumour – single-centre experience
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377415/
https://www.ncbi.nlm.nih.gov/pubmed/30783385
http://dx.doi.org/10.5114/wo.2018.81402
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