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Circulating tumor DNA as an early cancer detection tool

Journal

PHARMACOLOGY & THERAPEUTICS
Volume 207, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2019.107458

Keywords

Circulating tumor DNA; Early detection; Cell-free DNA; Cancer screening; Cancer detection

Funding

  1. National Cancer Institute (NCI) of the National Institutes of Health (NIH) [P30CA33572, K08CA234394]
  2. TGEN-City of Hope Precision Medicine Pilot Award
  3. City of Hope Cancer Control and Populations Sciences Pilot Award

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Circulating tumor DNA holds substantial promise as an early detection biomarker, particularly for cancers that do not have currently accepted screening methodologies, such as ovarian, pancreatic, and gastric cancers. Many features intrinsic to ctDNA analysis may be leveraged to enhance its use as an early cancer detection biomarker: including ctDNA fragment lengths, DNA copy number variations, and associated patient phenotypic information. Furthermore, ctDNA testing may be synergistically used with other multi-omic biomarkers to enhance early detection. For instance, assays may incorporate early detection proteins (i.e., CA-125), epigenetic markers, circulating tumor RNA, nucleosomes, exosomes, and associated immune markers. Many companies are currently competing to develop a marketable early cancer detection test that leverages ctDNA. Although some hurdles (like early stage disease assay accuracy, high implementation costs, confounding from clonal hematopoiesis, and lack of clinical utility studies) need to be addressed before integration into healthcare, ctDNA assays hold substantial potential as an early cancer screening test. (C) 2019 Elsevier Inc. All rights reserved.

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