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An approach for developing a blood-based screening panel for lung cancer based on clonal hematopoietic mutations
被引:0
|作者:
Anandakrishnan, Ramu
[1
,2
]
Shahidi, Ryan
[1
]
Dai, Andrew
[1
]
Antony, Veneeth
[1
]
Zyvoloski, Ian J.
[3
]
机构:
[1] Edward Via Coll Osteopath Med, Biomed Sci, Blacksburg, VA 24060 USA
[2] Virginia Tech, Maryland Virginia Coll Vet Med, Blacksburg, VA 24061 USA
[3] Univ Maryland, Baltimore, MD USA
来源:
关键词:
CLINICAL VALIDATION;
EXPRESSION;
IDENTIFICATION;
CELLS;
D O I:
10.1371/journal.pone.0307232
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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.
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