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通过新一代测序对难治性或耐药性浸润性乳腺癌进行分子特征分析

Molecular Characterization, Via Next-Generation Sequencing, of Refractory or Resistant Invasive Breast Carcinoma.

作者信息

Pose Lapausa Patricia, Soria Comes Teresa, Calabria Inés, Maestu Maiques Inmaculada

机构信息

Surgical Pathology, Hospital General Universitario, Valencia, ESP.

Oncology, Hospital Universitario de la Ribera, Alzira, ESP.

出版信息

Cureus. 2021 Nov 13;13(11):e19528. doi: 10.7759/cureus.19528. eCollection 2021 Nov.

Abstract

The most frequently diagnosed neoplasia in the world in 2020 was breast cancer (BC). On top of its high incidence, unexpected behavior as recurrence in patients, in spite of appropriate therapies, reaches 20%-30%. We believe that some molecular characteristics of tumors may lead to this bad behavior, and we can identify them with next-generation sequencing (NGS). We made a retrospective multicentric study, conducted to molecularly characterize, by means of a custom NGS panel, cases diagnosed with treatment-refractory or treatment-resistant invasive breast carcinoma, studied in formalin-fixed paraffin-embedded (FFPE) samples. The panel included 50 genes related to tumorigenesis, cancer evolution and targeted therapies. Twelve cases were included from three centers. Alterations of driver genes were found in all of the cases, and 75% harbored mutations in TP53. Furthermore, we found alterations that could be therapeutic targets in half of the patients, such as mutations in PIK3CA (33% cases), mTOR (8.3%) or BRCA1 (8.3%). Other significant molecular alterations were: the loss of SWI-SNF complex´s components, modified genes of the MAP kinase pathway and alterations in epidermal growth factor receptor (EGFR). Not all of them are known targets but prognostic significance was found. We conclude that NGS characterization of breast cancer in FFPE samples is a reproducible technique that can provide prognostic and predictive information about our patients and therefore, constitutes, in the near future, a valuable clinical tool in the context of precision medicine.

摘要

2020年全球诊断出的最常见肿瘤是乳腺癌(BC)。除了其高发病率外,尽管进行了适当治疗,但患者复发的意外情况发生率仍达到20%-30%。我们认为肿瘤的某些分子特征可能导致这种不良行为,并且我们可以通过下一代测序(NGS)来识别它们。我们进行了一项回顾性多中心研究,通过定制的NGS面板,对福尔马林固定石蜡包埋(FFPE)样本中诊断为治疗难治性或治疗抵抗性浸润性乳腺癌的病例进行分子特征分析。该面板包括50个与肿瘤发生、癌症进展和靶向治疗相关的基因。从三个中心纳入了12例病例。在所有病例中均发现了驱动基因的改变,75%的病例TP53存在突变。此外,我们在一半的患者中发现了可能成为治疗靶点的改变,例如PIK3CA(33%的病例)、mTOR(8.3%)或BRCA1(8.3%)的突变。其他显著的分子改变包括:SWI-SNF复合物成分的缺失、MAP激酶途径的修饰基因以及表皮生长因子受体(EGFR)的改变。并非所有这些都是已知靶点,但发现了其预后意义。我们得出结论,FFPE样本中乳腺癌的NGS特征分析是一种可重复的技术,能够为我们的患者提供预后和预测信息,因此在不久的将来,它将成为精准医学背景下一种有价值的临床工具。

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