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Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age

INTRODUCTION: The purpose of the present study was to characterise patients with breast cancer (BC) and NOD2-mutation (age ≥ 50 years) according to their clinicopathological factors or family history. Patients aged ≥ 50 years were compared with the control group and with NOD2-mutation carriers aged...

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Autores principales: Huszno, Joanna, Kolosza, Zofia, Nycz-Bochenek, Marta, Lisik, Małgorzata, Mazur, Magdalena, Pamuła-Piłat, Jolanta, Grzybowska, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403763/
https://www.ncbi.nlm.nih.gov/pubmed/32774132
http://dx.doi.org/10.5114/wo.2020.97475
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author Huszno, Joanna
Kolosza, Zofia
Nycz-Bochenek, Marta
Lisik, Małgorzata
Mazur, Magdalena
Pamuła-Piłat, Jolanta
Grzybowska, Ewa
author_facet Huszno, Joanna
Kolosza, Zofia
Nycz-Bochenek, Marta
Lisik, Małgorzata
Mazur, Magdalena
Pamuła-Piłat, Jolanta
Grzybowska, Ewa
author_sort Huszno, Joanna
collection PubMed
description INTRODUCTION: The purpose of the present study was to characterise patients with breast cancer (BC) and NOD2-mutation (age ≥ 50 years) according to their clinicopathological factors or family history. Patients aged ≥ 50 years were compared with the control group and with NOD2-mutation carriers aged < 50 years. MATERIAL AND METHODS: Prognostic factors were analysed in patients with BC with confirmed NOD2 c.3016_3017insC (n = 150) mutations. The control group was selected from patients with BC without mutations (n = 376). RESULTS: There were significant differences between NOD2-mutation carriers and the control group aged ≥ 50 years, according to HER2 overexpression (p = 0.0001), ER (–) (p = 0.007), PR (–) (p = 0.003), T1–T2 (p = 0.011), and G3 (p = 0.036). Similarly, significant differences were observed between NOD2-mutation carriers and the control group aged < 50 years, according to HER2 overexpression (p = 0.0001), ER (–) (p = 0.049), and N (+) (p = 0.038). In patients aged ≥ 50 years, family history of cancer, including BC, was observed more often in NOD2-mutation carriers compared with the control group of patients (OR = 1.66; p = 0.072, for BC in family history: OR = 2.65; p = 0.002). NOD2-mutation carriers aged ≥ 50 years had significantly less frequent G3 (p = 0.004) and HER2 overexpression (p = 0.043) compared with patients with NOD2 mutation aged < 50 years. CONCLUSIONS: The presence of the NOD2 mutation is not only characteristic of younger patients but also in patients > 50 years of age. In NOD2-mutation carriers aged ≥ 50 years, the presence of larger tumour size, G3, or HER2 overexpression were lower compared with younger patients with NOD2 mutation.
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spelling pubmed-74037632020-08-07 Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age Huszno, Joanna Kolosza, Zofia Nycz-Bochenek, Marta Lisik, Małgorzata Mazur, Magdalena Pamuła-Piłat, Jolanta Grzybowska, Ewa Contemp Oncol (Pozn) Original Paper INTRODUCTION: The purpose of the present study was to characterise patients with breast cancer (BC) and NOD2-mutation (age ≥ 50 years) according to their clinicopathological factors or family history. Patients aged ≥ 50 years were compared with the control group and with NOD2-mutation carriers aged < 50 years. MATERIAL AND METHODS: Prognostic factors were analysed in patients with BC with confirmed NOD2 c.3016_3017insC (n = 150) mutations. The control group was selected from patients with BC without mutations (n = 376). RESULTS: There were significant differences between NOD2-mutation carriers and the control group aged ≥ 50 years, according to HER2 overexpression (p = 0.0001), ER (–) (p = 0.007), PR (–) (p = 0.003), T1–T2 (p = 0.011), and G3 (p = 0.036). Similarly, significant differences were observed between NOD2-mutation carriers and the control group aged < 50 years, according to HER2 overexpression (p = 0.0001), ER (–) (p = 0.049), and N (+) (p = 0.038). In patients aged ≥ 50 years, family history of cancer, including BC, was observed more often in NOD2-mutation carriers compared with the control group of patients (OR = 1.66; p = 0.072, for BC in family history: OR = 2.65; p = 0.002). NOD2-mutation carriers aged ≥ 50 years had significantly less frequent G3 (p = 0.004) and HER2 overexpression (p = 0.043) compared with patients with NOD2 mutation aged < 50 years. CONCLUSIONS: The presence of the NOD2 mutation is not only characteristic of younger patients but also in patients > 50 years of age. In NOD2-mutation carriers aged ≥ 50 years, the presence of larger tumour size, G3, or HER2 overexpression were lower compared with younger patients with NOD2 mutation. Termedia Publishing House 2020-07-03 2020 /pmc/articles/PMC7403763/ /pubmed/32774132 http://dx.doi.org/10.5114/wo.2020.97475 Text en Copyright © 2020 Termedia 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 (http://creativecommons.org/licenses/by-nc-sa/4.0/)
spellingShingle Original Paper
Huszno, Joanna
Kolosza, Zofia
Nycz-Bochenek, Marta
Lisik, Małgorzata
Mazur, Magdalena
Pamuła-Piłat, Jolanta
Grzybowska, Ewa
Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age
title Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age
title_full Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age
title_fullStr Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age
title_full_unstemmed Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age
title_short Clinicopathological characteristics of breast cancer patients with NOD2 mutation according to age
title_sort clinicopathological characteristics of breast cancer patients with nod2 mutation according to age
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403763/
https://www.ncbi.nlm.nih.gov/pubmed/32774132
http://dx.doi.org/10.5114/wo.2020.97475
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