Early Detection of Molecular Residual Disease in Localized Lung Cancer by Circulating Tumor DNA Profiling
Stanford Medicine · Stanford University · +2 more institutions
Abstract
Abstract Identifying molecular residual disease (MRD) after treatment of localized lung cancer could facilitate early intervention and personalization of adjuvant therapies. Here, we apply cancer personalized profiling by deep sequencing (CAPP-seq) circulating tumor DNA (ctDNA) analysis to 255 samples from 40 patients treated with curative intent for stage I–III lung cancer and 54 healthy adults. In 94% of evaluable patients experiencing recurrence, ctDNA was detectable in the first posttreatment blood sample, indicating reliable identification of MRD. Posttreatment ctDNA detection preceded radiographic progression in 72% of patients by a median of 5.2 months, and 53% of patients harbored ctDNA mutation…
Citation impact
- FWCI
- 22.70
- Percentile
- 100%
- References
- 34
Authors
27- AAAadel A. Chaudhuri
Stanford Medicine, Stanford University
- JJJacob J. Chabon
California Institute for Regenerative Medicine, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University
- AFAlexander F. Lovejoy
Stanford Medicine, Stanford University
- AMAaron M. Newman
California Institute for Regenerative Medicine, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University
- HSHenning Stehr
Stanford University
Topics & keywords
- Medicine
- Circulating tumor DNA
- Lung cancer
- Oncology
- Minimal residual disease
- Internal medicine
- Cancer
- Disease
- Good health and well-being