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

被引:2
作者
Sese, Marta [1 ,6 ]
Somoza, Rosa [1 ]
Maestu, Inmaculada [2 ]
Martin Ureste, Maria [2 ]
Sanchez, Alfredo [3 ]
Felipe Cordoba, Juan [4 ]
Sansano, Irene [5 ]
Venturas, Griselda [5 ]
Ramon y Cajal, Santiago [1 ,5 ,6 ]
Hernandez-Losa, Javier [1 ,5 ,6 ]
机构
[1] Univ Autonoma Barcelona, VHIR, Translat Mol Pathol, Barcelona, Spain
[2] Hosp Univ Doctor Peset, Dept Med Oncol, Valencia, Spain
[3] Consorci Hosp Prov Castello, Dept Med Oncol, Castellon de La Plana, Spain
[4] Hosp Arnau Vilanova, Dept Med Oncol, Lleida, Spain
[5] Hosp Univ Vall dHebron, Dept Pathol, Barcelona, Spain
[6] Spanish Biomed Res Network Ctr Oncol CIBERONC, Barcelona, Spain
关键词
Blood collection tubes; cfDNA; EGFR mutation analysis; NSCLC; CIRCULATING TUMOR DNA; LUNG-CANCER; SAMPLE STORAGE; PLASMA; CHEMOTHERAPY; AZD9291;
D O I
10.1007/s40487-019-00099-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 (R) 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 (R) 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.
引用
收藏
页码:131 / 139
页数:9
相关论文
共 35 条
  • [1] Concordance of Mutation Detection in Circulating Tumor DNA in Early Clinical Trials Using Different Blood Collection Protocols
    Ahlborn, Lise B.
    Madsen, Mette
    Jonson, Lars
    Nielsen, Finn C.
    Lassen, Ulrik
    Yde, Christina W.
    Mau-Sorensen, Morten
    [J]. CLINICAL LABORATORY, 2017, 63 (10) : 1755 - 1759
  • [2] Clinical Applications of Circulating Tumor Cells and Circulating Tumor DNA as Liquid Biopsy
    Alix-Panabieres, Catherine
    Pantel, Klaus
    [J]. CANCER DISCOVERY, 2016, 6 (05) : 479 - 491
  • [3] Clinical Validation of a PCR Assay for the Detection of EGFR Mutations in Non-Small-Cell Lung Cancer: Retrospective Testing of Specimens from the EURTAC Trial
    Benlloch, Susana
    Luisa Botero, Maria
    Beltran-Alamillo, Jordi
    Mayo, Clara
    Gimenez-Capitan, Ana
    de Aguirre, Itziar
    Queralt, Cristina
    Luis Ramirez, Jose
    Ramon y Cajal, Santiago
    Klughammer, Barbara
    Schlegel, Mariette
    Bordogna, Walter
    Chen, David
    Zhang, Guili
    Kovach, Barbara
    Shieh, Felice
    Palma, John F.
    Wu, Lin
    Lawrence, H. Jeffrey
    Taron, Miquel
    [J]. PLOS ONE, 2014, 9 (02):
  • [4] Liquid biopsy: monitoring cancer-genetics in the blood
    Crowley, Emily
    Di Nicolantonio, Federica
    Loupakis, Fotios
    Bardelli, Alberto
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2013, 10 (08) : 472 - 484
  • [5] Performance of Streck cfDNA Blood Collection Tubes for Liquid Biopsy Testing
    Diaz, Inga Medina
    Nocon, Annette
    Mehnert, Daniel H.
    Fredebohm, Johannes
    Diehl, Frank
    Holtrup, Frank
    [J]. PLOS ONE, 2016, 11 (11):
  • [6] Liquid Biopsies: Genotyping Circulating Tumor DNA
    Diaz, Luis A.
    Bardelli, Alberto
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (06) : 579 - +
  • [7] A new methodology to preserve the original proportion and integrity of cell-free fetal DNA in maternal plasma during sample processing and storage
    Fernando, M. R.
    Chen, K.
    Norton, S.
    Krzyzanowski, G.
    Bourne, D.
    Hunsley, B.
    Ryan, W. L.
    Bassett, C.
    [J]. PRENATAL DIAGNOSIS, 2010, 30 (05) : 418 - 424
  • [8] AZD9291 in TKI EGFR resistance in non-small cell lung cancer and the new concept of phase I trials
    Gil-Bazo, Ignacio
    Rolfo, Christian
    [J]. TRANSLATIONAL LUNG CANCER RESEARCH, 2016, 5 (01) : 85 - 88
  • [9] Liquid Biopsy Preservation Solutions for Standardized Pre-Analytical Workflows-Venous Whole Blood and Plasma
    Groelz, Daniel
    Hauch, Siegfried
    Schlumpberger, Martin
    Guenther, Kalle
    Voss, Thorsten
    Sprenger-Haussels, Markus
    Oelmueller, Uwe
    [J]. CURRENT PATHOBIOLOGY REPORTS, 2018, 6 (04) : 275 - 286
  • [10] Circulating Tumor DNA as a Liquid Biopsy for Cancer
    Heitzer, Ellen
    Ulz, Peter
    Geigl, Jochen B.
    [J]. CLINICAL CHEMISTRY, 2015, 61 (01) : 112 - 123