Evidence map›Paper›PMID 33428651›Full record

ArticlePloS one2021

Robust radiogenomics approach to the identification of EGFR mutations among patients with NSCLC from three different countries using topologically invariant Betti numbers.

Kenta Ninomiya, Hidetaka Arimura, Wai Yee Chan, Kentaro Tanaka, Shinichi Mizuno, Nadia Fareeda Muhammad Gowdh, Nur Adura Yaakup, Chong-Kin Liam, Chee-Shee Chai, Kwan Hoong Ng

Erratum issuedAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 4 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

11 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  8. Feature selection methods and predictive models in CT lung cancer radiomics.Journal of applied clinical medical physics · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Kenta NinomiyaDivision of Medical Quantum Science, Department of Health Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0000-0002-9566-4875
Hidetaka ArimuraFaculty of Medical Sciences, Division of Medical Quantum Science, Department of Health Sciences, Kyushu University, Fukuoka, Japan.
Wai Yee ChanFaculty of Medicine, Department of Biomedical Imaging, University of Malaya, Kuala Lumpur, Malaysia.
Kentaro TanakaDepartment of Respiratory Medicine, Kyushu University Hospital, Fukuoka, Japan.
Shinichi MizunoDivision of Medical Sciences and Technology, Department of Health Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Nadia Fareeda Muhammad GowdhFaculty of Medicine, Department of Biomedical Imaging, University of Malaya, Kuala Lumpur, Malaysia.ORCID 0000-0002-1534-6034
Nur Adura YaakupFaculty of Medicine, Department of Biomedical Imaging, University of Malaya, Kuala Lumpur, Malaysia.
Chong-Kin LiamFaculty of Medicine, Department of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Chee-Shee ChaiFaculty of Medicine and Health Science, Department of Medicine, University Malaysia Sarawak, Kota Samarahan, Sarawak, Malaysia.
Kwan Hoong NgFaculty of Medicine, Department of Biomedical Imaging, University of Malaya, Kuala Lumpur, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo propose a novel robust radiogenomics approach to the identification of epidermal growth factor receptor (EGFR) mutations among patients with non-small cell lung cancer (NSCLC) using Betti numbers (BNs). MATERIALS AND

methodsContrast enhanced computed tomography (CT) images of 194 multi-racial NSCLC patients (79 EGFR mutants and 115 wildtypes) were collected from three different countries using 5 manufacturers' scanners with a variety of scanning parameters. Ninety-nine cases obtained from the University of Malaya Medical Centre (UMMC) in Malaysia were used for training and validation procedures. Forty-one cases collected from the Kyushu University Hospital (KUH) in Japan and fifty-four cases obtained from The Cancer Imaging Archive (TCIA) in America were used for a test procedure. Radiomic features were obtained from BN maps, which represent topologically invariant heterogeneous characteristics of lung cancer on CT images, by applying histogram- and texture-based feature computations. A BN-based signature was determined using support vector machine (SVM) models with the best combination of features that maximized a robustness index (RI) which defined a higher total area under receiver operating characteristics curves (AUCs) and lower difference of AUCs between the training and the validation. The SVM model was built using the signature and optimized in a five-fold cross validation. The BN-based model was compared to conventional original image (OI)- and wavelet-decomposition (WD)-based models with respect to the RI between the validation and the test.

resultsThe BN-based model showed a higher RI of 1.51 compared with the models based on the OI (RI: 1.33) and the WD (RI: 1.29).

conclusionThe proposed model showed higher robustness than the conventional models in the identification of EGFR mutations among NSCLC patients. The results suggested the robustness of the BN-based approach against variations in image scanner/scanning parameters.

Indexed as

AdultAgedAged, 80 and overArea Under CurveCarcinoma, Non-Small-Cell LungErbB ReceptorsFemaleHumansImage Processing, Computer-AssistedJapanLung NeoplasmsMalaysiaMaleMiddle AgedMutationROC CurveEGFR protein, humanErbB Receptors

Identifiers

PMID33428651
PMCPMC7799813

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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.