Skip NavigationSkip to Content

Exosome-based detection of activating and resistance EGFR mutations from plasma of non-small cell lung cancer patients

  1. Author:
    Castellanos-Rizaldos, Elena
    Zhang, Xuan
    Tadigotla, Vasisht R
    Grimm, Dominik G
    Karlovich,Chris
    Raez, Luis E
    Skog, Johan K
  2. Author Address

    Exosome Diagnostics, a Bio-Techne brand, Waltham, Massachusetts, USA., Exosome Diagnostics, a Bio-Techne brand, Martinsried, Germany., Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, USA., Memorial Cancer Institute, Memorial Health Care System, Florida International University, Florida, USA.,
    1. Year: 2019
    2. Date: Apr 23
    3. Epub Date: 2019 04 23
  1. Journal: Oncotarget
    1. 10
    2. 30
    3. Pages: 2911-2920
  2. Type of Article: Article
  1. Abstract:

    Non-small cell lung cancer (NSCLC) is the most prevalent form of lung cancer and its molecular landscape has been extensively studied. The most common genetic alterations in NSCLC are mutations within the epidermal growth factor receptor (EGFR) gene, with frequencies between 10-40%. There are several molecular targeted therapies for patients harboring these mutations. Liquid biopsies constitute a flexible approach to monitor these mutations in real time as opposed to tissue biopsies that represent a single snap-shot in time. However, interrogating cell free DNA (cfDNA) has inherent biological limitations, especially at early or localized disease stages, where there is not enough tumor material released into the patient 39;s circulation. We developed a qPCR- based test (ExoDx EGFR) that interrogates mutations within EGFR using Exosomal RNA/DNA and cfDNA (ExoNA) derived from plasma in a cohort of 110 NSCLC patients. The performance of the assay yielded an overall sensitivity of 90% for L858R, 83% for T790M and 73% for exon 19 indels with specificities of 100%, 100%, and 96% respectively. In a subcohort of patients with extrathoracic disease (M1b and MX) the sensitivities were 92% (L858R), 95% (T790M), and 86% (exon 19 indels) with specificity of 100%, 100% and 94% respectively.

    See More

External Sources

  1. DOI: 10.18632/oncotarget.26885
  2. PMID: 31080561
  3. PMCID: PMC6499599
  4. PII : 26885

Library Notes

  1. Fiscal Year: FY2018-2019
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel