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在真实世界数据集中文本特征的胸腺瘤。

Genomic characterization of thymic epithelial tumors in a real-world dataset.

机构信息

Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan.

Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan.

出版信息

ESMO Open. 2023 Oct;8(5):101627. doi: 10.1016/j.esmoop.2023.101627. Epub 2023 Sep 12.

Abstract

BACKGROUND

Thymic epithelial tumors (TETs) are rare neoplasms arising in the mediastinum, including thymic carcinomas and thymomas. Due to their rarity, little is known about the genomic profiles of TETs. Herein, we investigated the genomic characteristics of TETs evaluated in a large comprehensive genomic profiling database in a real-world setting.

METHODS

We included data from two different cohorts: Foundation Medicine Inc. (FMI) in the United States and the Center for Cancer Genomics and Advanced Therapeutics (C-CAT) in Japan. Samples profiled were examined for all classes of alterations in 253 genes targeted across all assays. Tumor mutational burden (TMB) and microsatellite instability (MSI) were also evaluated.

RESULTS

A total of 794 patients were collected in our study, including 722 cases from FMI and 72 cases from C-CAT. In the FMI data, CDKN2A (39.9%), TP53 (30.2%) and CDKN2B (24.6%) were frequently altered in thymic carcinoma, versus TP53 (7.8%), DNMT3A (6.8%), and CDKN2A (5.8%) in thymoma. TMB-high (≥10 mutations/Mb) and MSI were present in 7.0% and 2.3% of thymic carcinomas, and 1.6% and 0.3% of thymomas, respectively. Within C-CAT data, CDKN2A (38.5%), TP53 (36.5%) and CDKN2B (30.8%) were also frequently altered in thymic carcinoma, while alterations of TSC1, SETD2 and LTK (20.0% each) were found in thymoma.

CONCLUSIONS

To the best of our knowledge, this is the largest cohort in which genomic alterations, TMB and MSI status of TETs were investigated. Potential targets for treatment previously unbeknownst in TETs are identified in this study, entailing newfound opportunities to advance therapeutic development.

摘要

背景

胸腺瘤(TET)是一种罕见的纵隔起源的上皮性肿瘤,包括胸腺癌和胸腺瘤。由于其罕见性,对 TET 的基因组特征知之甚少。在此,我们在真实环境下,通过大型综合基因组分析数据库,研究了 TET 的基因组特征。

方法

我们纳入了来自美国 Foundation Medicine Inc.(FMI)和日本癌症基因组和先进治疗中心(C-CAT)的两个不同队列的数据。对所有检测中靶向的 253 个基因的所有类别改变进行了样本分析。还评估了肿瘤突变负荷(TMB)和微卫星不稳定性(MSI)。

结果

本研究共收集了 794 例患者,其中 FMI 有 722 例,C-CAT 有 72 例。在 FMI 数据中,CDKN2A(39.9%)、TP53(30.2%)和 CDKN2B(24.6%)在胸腺癌中频繁改变,而在胸腺瘤中,TP53(7.8%)、DNMT3A(6.8%)和 CDKN2A(5.8%)则改变较少。TMB-高(≥10 突变/Mb)和 MSI 在胸腺癌中分别为 7.0%和 2.3%,在胸腺瘤中分别为 1.6%和 0.3%。在 C-CAT 数据中,CDKN2A(38.5%)、TP53(36.5%)和 CDKN2B(30.8%)在胸腺癌中也经常改变,而 TSC1、SETD2 和 LTK 的改变(各 20.0%)则在胸腺瘤中发现。

结论

据我们所知,这是研究 TET 基因组改变、TMB 和 MSI 状态的最大队列。本研究确定了 TET 中以前未知的治疗靶点,为推进治疗发展提供了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ad6/10594028/2949bb60b36c/gr1.jpg

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