Evidence map›Paper›PMID 39718015›Full record

ArticleCancer medicine2024

Machine Learning Enabled Prediction of Biologically Relevant Gene Expression Using CT-Based Radiomic Features in Non-Small Cell Lung Cancer.

Shrey S Sukhadia, Christoph Sadee, Olivier Gevaert, Shivashankar H Nagaraj

Abstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Insights into pet-based radiogenomics in oncology: an updated systematic review.European journal of nuclear medicine and molecular imaging · 2025
    Pooled it
  2. Pooled it
  3. Review
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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

4 authors.

Shrey S SukhadiaCentre for Genomics and Personalized Health and School of Biomedical Sciences, Queensland University of Technology, Brisbane, Queensland, Australia.
Christoph SadeeStanford Center for Biomedical Informatics Research, Department of Medicine and Biomedical Data Science, Stanford University, California, USA.
Olivier GevaertStanford Center for Biomedical Informatics Research, Department of Medicine and Biomedical Data Science, Stanford University, California, USA.
Shivashankar H NagarajCentre for Genomics and Personalized Health and School of Biomedical Sciences, Queensland University of Technology, Brisbane, Queensland, Australia.ORCID 0000-0003-3463-6835

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-small-cell lung cancer (NSCLC) remains a global health challenge, driving morbidity and mortality. The emerging field of radiogenomics utilizes statistical methods to correlate radiographic tumor features with genomic characteristics from biopsy samples. Radiomic techniques automate the precise extraction of imaging features from tumor regions in radiographic scans, which are subjected to machine learning (ML) to predict genomic attributes.

methodsIn a retrospective study of two NSCLC patient cohorts separated by 5 years, we performed a radiogenomic analysis of previously disseminated data from 2018 (n = 116) and newly acquired data from 2023 (n = 44) using RNA sequencing and lung CT images. Combining the data from two cohorts post binarization (of gene expression) or batch normalization (of radiomic features) in each cohort proved to be a better approach as compared to training the model on one cohort and validating on the other.

resultsOur ML-based radiogenomic modeling identified specific imaging features-wavelet, three-dimensional local binary patterns, and logarithmic sigma of gray-level variance-as predictive indicators for high (1) vs. low (0) gene expression of pivotal NSCLC-related genes: SLC35C1, BCL2L1, and MAPK1. These genes have recognized implications in a variety of biological pathways and mechanisms of drug resistance pertinent to NSCLC.

conclusionThe successful integration of heterogeneous radiogenomic datasets underscores the potential of imaging biomarkers in uncovering NSCLC biological processes through gene expression profiles.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMachine LearningTomography, X-Ray ComputedAgedBiomarkers, TumorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedRadiomicsRetrospective StudiesBiomarkers, Tumorgene expression and non‐small cell lung cancermachine learningradiogenomicsradiomics

Identifiers

PMID39718015
PMCPMC11667219

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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.