Evidence map›Paper›PMID 39172974›Full record

ArticlePloS one2024

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

Ramu Anandakrishnan, Ryan Shahidi, Andrew Dai, Veneeth Antony, Ian J Zyvoloski

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ramu AnandakrishnanEdward Via College of Osteopathic Medicine, Biomedical Sciences, Blacksburg, Virginia, United States of America.ORCID 0000-0003-0422-3984
Ryan ShahidiEdward Via College of Osteopathic Medicine, Biomedical Sciences, Blacksburg, Virginia, United States of America.
Andrew DaiEdward Via College of Osteopathic Medicine, Biomedical Sciences, Blacksburg, Virginia, United States of America.
Veneeth AntonyEdward Via College of Osteopathic Medicine, Biomedical Sciences, Blacksburg, Virginia, United States of America.
Ian J ZyvoloskiUniversity of Maryland, Baltimore, Maryland, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Early Detection of CancerLung NeoplasmsMutationAgedBiomarkers, TumorFemaleHumansLogistic ModelsMachine LearningMaleMiddle AgedBiomarkers, Tumor

Identifiers

PMID39172974
PMCPMC11341013

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.