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Nat Commun ; 12(1): 5060, 2021 08 20.
Article in English | MEDLINE | ID: mdl-34417454

ABSTRACT

Non-invasive approaches for cell-free DNA (cfDNA) assessment provide an opportunity for cancer detection and intervention. Here, we use a machine learning model for detecting tumor-derived cfDNA through genome-wide analyses of cfDNA fragmentation in a prospective study of 365 individuals at risk for lung cancer. We validate the cancer detection model using an independent cohort of 385 non-cancer individuals and 46 lung cancer patients. Combining fragmentation features, clinical risk factors, and CEA levels, followed by CT imaging, detected 94% of patients with cancer across stages and subtypes, including 91% of stage I/II and 96% of stage III/IV, at 80% specificity. Genome-wide fragmentation profiles across ~13,000 ASCL1 transcription factor binding sites distinguished individuals with small cell lung cancer from those with non-small cell lung cancer with high accuracy (AUC = 0.98). A higher fragmentation score represented an independent prognostic indicator of survival. This approach provides a facile avenue for non-invasive detection of lung cancer.


Subject(s)
Circulating Tumor DNA/metabolism , DNA Fragmentation , Lung Neoplasms/diagnosis , Lung Neoplasms/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Apoptosis , Carcinoma, Non-Small-Cell Lung/diagnosis , Carcinoma, Non-Small-Cell Lung/genetics , Carcinoma, Non-Small-Cell Lung/pathology , Cell Line, Tumor , Diagnosis, Differential , Early Detection of Cancer , Female , Genome, Human , Humans , Lung Neoplasms/pathology , Male , Middle Aged , Models, Biological , Neoplasm Metastasis , Neoplasm Staging , Small Cell Lung Carcinoma/diagnosis , Small Cell Lung Carcinoma/genetics , Small Cell Lung Carcinoma/pathology , Young Adult
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