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

被引:3
作者
Huszno, Joanna [1 ]
Kolosza, Zofia [2 ]
Nycz-Bochenek, Marta [1 ]
Lisik, Matgorzata [1 ]
Mazur, Magdalena [3 ]
Pamula-Pitat, Jolanta [3 ]
Grzybowska, Ewa [4 ]
机构
[1] Maria Sklodowska Curie Natl Res Inst Oncol, Gliwice Branch, Genet Outpatient Clin, 15 Wybrzeze Armii Krajowej St, PL-44101 Gliwice, Poland
[2] Maria Sklodowska Curie Natl Res Inst Oncol, Gliwice Branch, Dept Biostat & Bioinformat, Gliwice, Poland
[3] Maria Sklodowska Curie Natl Res Inst Oncol, Gliwice Branch, Dept Genet & Mol Diagnost Canc, Gliwice, Poland
[4] Maria Sklodowska Curie Natl Res Inst Oncol, Gliwice Branch, Ctr Translat Res & Mol Biol Canc, Gliwice, Poland
来源
WSPOLCZESNA ONKOLOGIA-CONTEMPORARY ONCOLOGY | 2020年 / 24卷 / 02期
关键词
breast cancer; NOD2; mutation; family history of cancer; 3020INSC MUTATION; PREDISPOSES; ALLELE;
D O I
10.5114/wo.2020.97475
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:79 / 86
页数:8
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