| Literature DB >> 31036768 |
Jeong-Seon Ryu1, Jun Hyeok Lim2, Myoung Kyu Lee3, Seung Jae Lee4, Hyun-Jung Kim2, Min Jeong Kim2, Mi Hwa Park2, Jung Soo Kim2, Hae-Seong Nam2, Nuri Park2, Seok Joong Yong2.
Abstract
A blood-based approach such as circulating tumor DNA remains challenging in diagnosis for early-stage disease. Bronchial washing (BW) is a minimally invasive procedure that yields fluids that may contain tumor DNA. Therefore, we prospectively enrolled 12 patients with early-stage non-small cell lung cancer without endoscopically visible tumors. Somatic mutations were analyzed using ultra-deep next-generation sequencing in 48 paired specimens (primary tumor tissue, normal tissue, BW supernatant, and BW precipitate). In primary tumors, 130 missense mutations/indels (5-16 per patient) and 20 driver mutations (0-3 per patient) were found. Concordance of driver mutations between BW fluids and primary tumors was 95.0%. The allele frequencies for missense mutations/indels in BW supernatants significantly correlated with those in primary tumors and were higher than those in BW precipitates. These findings suggest that BW supernatants are reflective of tumor-associated mutations and could be used for early-stage lung cancer diagnosis. © AlphaMed Press 2019.Entities:
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Year: 2019 PMID: 31036768 PMCID: PMC6656449 DOI: 10.1634/theoncologist.2019-0147
Source DB: PubMed Journal: Oncologist ISSN: 1083-7159