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胚系 TP53 基因突变检测在早发性乳腺癌中的应用:一项全国性队列研究的结果。

TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

机构信息

Department of Genetics, University Medical Center Utrecht, PO Box 85090, 3508 AB, Utrecht, The Netherlands.

Family Cancer Clinic, Netherlands Cancer Institute, Amsterdam, The Netherlands.

出版信息

Fam Cancer. 2019 Apr;18(2):273-280. doi: 10.1007/s10689-018-00118-0.

Abstract

Early-onset breast cancer may be due to Li-Fraumeni Syndrome (LFS). Current national and international guidelines recommend that TP53 genetic testing should be considered for women with breast cancer diagnosed before the age of 31 years. However, large studies investigating TP53 mutation prevalence in this population are scarce. We collected nationwide laboratory records for all young breast cancer patients tested for TP53 mutations in the Netherlands. Between 2005 and 2016, 370 women diagnosed with breast cancer younger than 30 years of age were tested for TP53 germline mutations, and eight (2.2%) were found to carry a (likely) pathogenic TP53 sequence variant. Among BRCA1/BRCA2 mutation negative women without a family history suggestive of LFS or a personal history of multiple LFS-related tumours, the TP53 mutation frequency was < 1% (2/233). Taking into consideration that TP53 mutation prevalence was comparable or even higher in some studies selecting patients with breast cancer onset at older ages or HER2-positive breast cancers, raises the question of whether a very early age of onset is an appropriate single TP53 genetic testing criterion.

摘要

早发性乳腺癌可能是由于 Li-Fraumeni 综合征(LFS)引起的。目前,国家和国际指南建议,对于 31 岁以下诊断为乳腺癌的女性,应考虑进行 TP53 基因检测。然而,在这一人群中进行 TP53 突变流行率的大型研究却很少。我们收集了荷兰全国范围内所有接受 TP53 基因突变检测的年轻乳腺癌患者的实验室记录。在 2005 年至 2016 年间,对 370 名年龄小于 30 岁诊断为乳腺癌的女性进行了 TP53 种系突变检测,发现 8 名(2.2%)携带(可能)致病性 TP53 序列变异。在 BRCA1/BRCA2 突变阴性且无提示 LFS 的家族史或多个 LFS 相关肿瘤个人史的女性中,TP53 突变频率<1%(2/233)。考虑到在一些选择年龄较大的乳腺癌发病或 HER2 阳性乳腺癌患者的研究中,TP53 突变的流行率相当或更高,这就提出了一个问题,即非常早的发病年龄是否是一个合适的单一 TP53 基因检测标准。

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