An approach for developing a blood-based screening panel for lung cancer based on clonal hematopoietic mutations

PLoS One. 2024 Aug 22;19(8):e0307232. doi: 10.1371/journal.pone.0307232. eCollection 2024.

Abstract

Early detection can significantly reduce mortality due to lung cancer. Presented here is an approach for developing a blood-based screening panel based on clonal hematopoietic mutations. Animal model studies suggest that clonal hematopoietic mutations in tumor infiltrating immune cells can modulate cancer progression, representing potential predictive biomarkers. The goal of this study was to determine if the clonal expansion of these mutations in blood samples could predict the occurrence of lung cancer. A set of 98 potentially pathogenic clonal hematopoietic mutations in tumor infiltrating immune cells were identified using sequencing data from lung cancer samples. These mutations were used as predictors to develop a logistic regression machine learning model. The model was tested on sequencing data from a separate set of 578 lung cancer and 545 non-cancer samples from 18 different cohorts. The logistic regression model correctly classified lung cancer and non-cancer blood samples with 94.12% sensitivity (95% Confidence Interval: 92.20-96.04%) and 85.96% specificity (95% Confidence Interval: 82.98-88.95%). Our results suggest that it may be possible to develop an accurate blood-based lung cancer screening panel using this approach. Unlike most other "liquid biopsies" currently under development, the approach presented here is based on standard sequencing protocols and uses a relatively small number of rationally selected mutations as predictors.

MeSH terms

  • Aged
  • Biomarkers, Tumor / blood
  • Biomarkers, Tumor / genetics
  • Early Detection of Cancer* / methods
  • Female
  • Humans
  • Logistic Models
  • Lung Neoplasms* / blood
  • Lung Neoplasms* / diagnosis
  • Lung Neoplasms* / genetics
  • Machine Learning
  • Male
  • Middle Aged
  • Mutation*

Substances

  • Biomarkers, Tumor

Grants and funding

This work was funded by the VCOM 2023 REAP grant #1038624(RA). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.