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循环游离 DNA 突变在间变性甲状腺癌中的临床应用。

Clinical Utility of Circulating Cell-Free DNA Mutations in Anaplastic Thyroid Carcinoma.

机构信息

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Department of Endocrinology, Diabetes and Metabolism, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Thyroid. 2021 Aug;31(8):1235-1243. doi: 10.1089/thy.2020.0296. Epub 2021 Apr 19.

Abstract

Anaplastic thyroid carcinoma (ATC) is an aggressive thyroid cancer that requires a rapid diagnosis and treatment to achieve disease control. Gene mutation profiling of circulating cell-free DNA (cfDNA) in peripheral blood may help to facilitate early diagnosis and treatment selection. The relatively rapid turnaround time compared with conventional tumor mutation testing is a major advantage. The objectives of this study were to examine the concordance of ATC-related mutations detected in cfDNA with those detected in the corresponding tumor tissue, and to determine the prognostic significance of cfDNA mutations in ATC patients. The ATC patients who were diagnosed and treated at The University of Texas MD Anderson Cancer Center between January 2015 and February 2018 and who had cfDNA testing were included in this study. cfDNA was collected by blood draw and was analyzed by next-generation sequencing (NGS) using the Guardant360-73 gene platform. A total of 87 patients were included in the study. The most frequently mutated genes detected in cfDNA were , and . In 28 treatment naive ATC patients, the concordance rate of detected mutations in , and between cfDNA and matched tissue NGS was 82.1%, 92.9%, and 92.9%, respectively. Patients with a mutation detected on cfDNA had worse overall survival (OS) ( = 0.03). This association was observed across various treatment modalities, including surgery, cytotoxic chemotherapy, radiation, and BRAF inhibitor (BRAFi) therapy. With regard to treatment, BRAFi therapy significantly improved ATC OS ( = 0.003). cfDNA is a valuable tool to evaluate a tumor's molecular profile in ATC patients. We identified high concordance rates between the gene mutations identified via cfDNA analysis and those identified from the NGS of the corresponding tumor tissue sequencing. Identified mutations in cfDNA can potentially provide timely information to guide treatment selection and evaluate the prognosis in patients with ATC.

摘要

间变性甲状腺癌(ATC)是一种侵袭性甲状腺癌,需要快速诊断和治疗以控制疾病。外周血循环无细胞游离 DNA(cfDNA)的基因突变分析可能有助于早期诊断和治疗选择。与传统肿瘤突变检测相比,其相对较快的周转时间是一个主要优势。本研究的目的是检查 cfDNA 中检测到的与相应肿瘤组织中检测到的 ATC 相关突变的一致性,并确定 cfDNA 突变在 ATC 患者中的预后意义。

在 2015 年 1 月至 2018 年 2 月期间在德克萨斯大学 MD 安德森癌症中心诊断和治疗的 ATC 患者,并进行了 cfDNA 检测,这些患者被纳入本研究。通过采血收集 cfDNA,并使用 Guardant360-73 基因平台进行下一代测序(NGS)分析。本研究共纳入 87 例患者。在 cfDNA 中检测到的最常见突变基因是 、 、 和 。在 28 例未经治疗的 ATC 患者中,cfDNA 和匹配组织 NGS 中检测到的 、 和 突变的一致性率分别为 82.1%、92.9%和 92.9%。在 cfDNA 上检测到 突变的患者总体生存率(OS)更差(=0.03)。这种关联在包括手术、细胞毒性化疗、放疗和 BRAF 抑制剂(BRAFi)治疗在内的各种治疗方式中均观察到。关于治疗,BRAFi 治疗显著改善了 ATC 的 OS(=0.003)。

cfDNA 是评估 ATC 患者肿瘤分子谱的有价值工具。我们发现通过 cfDNA 分析鉴定的基因突变与通过相应肿瘤组织测序的 NGS 鉴定的基因突变之间具有很高的一致性。cfDNA 中鉴定的突变可能为指导治疗选择和评估 ATC 患者的预后提供及时的信息。

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