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用于测定非小细胞肺癌患者液体活检中EGFR突变状态的游离DNA收集管的验证

Validation of Cell-Free DNA Collection Tubes for Determination of EGFR Mutation Status in Liquid Biopsy from NSCLC Patients.

作者信息

Sesé Marta, Somoza Rosa, Maestu Inmaculada, Ureste Maria Martín, Sanchez Alfredo, Cordoba Juan Felipe, Sansano Irene, Venturas Griselda, Ramón Y Cajal Santiago, Hernández-Losa Javier

机构信息

Translational Molecular Pathology, Vall d'Hebron Institute of Research (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain.

Spanish Biomedical Research Network Centre in Oncology (CIBERONC), Barcelona, Spain.

出版信息

Oncol Ther. 2019 Dec;7(2):131-139. doi: 10.1007/s40487-019-00099-9. Epub 2019 Aug 19.

Abstract

INTRODUCTION

Precision medicine has revolutionized the understanding and treatment of cancer by identifying subsets of patients who are amenable to specific treatments according to their molecular characteristics, as exemplified by epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC). Although tissue biopsy is the gold standard for determining molecular alterations in tumors, its limitations have prompted the development of new techniques for studying tumor biomarkers in liquid biopsies, such as mutation analysis in cell-free DNA (cfDNA). cfDNA analysis can accurately determine tumor progression and prognosis and more effectively identify appropriate targeted therapies. However, cfDNA is vulnerable, particularly during plasma sample shipping.

OBJECTIVE

We compared the cell- and DNA-stabilizing properties of cell-free DNA blood collection tubes (BCTs) with those of the traditional shipping method (frozen plasma) for EGFR mutation testing using the cobas EGFR Mutation Test v2 in a prospective cohort of 49 patients from three different Spanish hospitals.

METHODS

In total, 98 NSCLC samples, two from each patient, were studied; five of the 49 cases were considered invalid by cobas with one of the two shipping methods analyzed. After excluding these samples, we analyzed 88 samples from 44 patients. Considering the current methodology (frozen plasma) for sending samples as the gold standard, we evaluated the sensitivity and specificity of cfDNA BCT shipment.

RESULTS

The global agreement between the two methods was 95.4%, with 100% sensitivity and 94.6% specificity for the cfDNA BCTs. cfDNA BCTs had a positive predictive value of 81.8% and negative predictive value of 100%.

CONCLUSION

cfDNA BCTs have the same sensitivity for EGFR mutation analysis in liquid biopsy as the current methodology and very high specificity. They also have some additional advantages in terms of collection and further shipment. Therefore, cfDNA BCTs can be perfectly incorporated into the routine practice for EGFR mutation determination.

FUNDING

Roche Farma S.A., Spain.

摘要

引言

精准医学通过识别根据分子特征适合特定治疗的患者亚组,彻底改变了癌症的理解和治疗方式,非小细胞肺癌(NSCLC)中的表皮生长因子受体(EGFR)突变就是例证。尽管组织活检是确定肿瘤分子改变的金标准,但其局限性促使了用于研究液体活检中肿瘤生物标志物的新技术的发展,如游离DNA(cfDNA)中的突变分析。cfDNA分析可以准确确定肿瘤进展和预后,并更有效地识别合适的靶向治疗。然而,cfDNA很脆弱,尤其是在血浆样本运输过程中。

目的

我们在来自西班牙三家不同医院的49名患者的前瞻性队列中,使用cobas EGFR突变检测v2,比较了游离DNA采血试管(BCT)与传统运输方法(冷冻血浆)在EGFR突变检测中的细胞和DNA稳定特性。

方法

总共研究了98份NSCLC样本,每位患者两份;在分析的两种运输方法中,49例中有5例被cobas判定为无效。排除这些样本后,我们分析了来自44名患者的88份样本。以当前发送样本的方法(冷冻血浆)作为金标准,我们评估了cfDNA BCT运输的敏感性和特异性。

结果

两种方法的总体一致性为95.4%;cfDNA BCT的敏感性为100%,特异性为94.6%。cfDNA BCT的阳性预测值为81.8%,阴性预测值为100%。

结论

cfDNA BCT在液体活检中进行EGFR突变分析的敏感性与当前方法相同,且特异性非常高。它们在采集和进一步运输方面也有一些额外优势。因此,cfDNA BCT可以完美地纳入EGFR突变测定的常规实践中。

资金来源

西班牙罗氏制药公司。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e6/7360002/ac5dcdb5e8b7/40487_2019_99_Fig1_HTML.jpg

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