Evidence map›Paper›PMID 36173022›Full record

ArticleJournal of applied clinical medical physics2022

Uniqueness of radiomic features in non-small cell lung cancer.

Gary Ge, Jie Zhang

Abstract read
In one paragraph

Article in Journal of applied clinical medical physics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Uniqueness of radiomic features in non-small cell lung cancer.Journal of applied clinical medical physics · 2022
    Article
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

2 authors.

Gary GeDepartment of Radiology, University of Kentucky, Lexington, Kentucky, 40536, USA.
Jie ZhangDepartment of Radiology, University of Kentucky, Lexington, Kentucky, 40536, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe uniqueness of radiomic features, combined with their reproducibility, determines the reliability of radiomic studies. This study is to test the hypothesis that radiomic features extracted from a defined region of interest (ROI) are unique to the underlying structure (e.g., tumor). APPROACH: Two cohorts of non-small cell lung cancer (NSCLC) patients were retrospectively retrieved from a GE and a Siemens CT scanner. The lung nodules (ROI) were delineated manually and radiomic features were extracted using IBEX. The same ROI was then translocated randomly to four other tissue regions of the same set of images: adipose, heart, lung beyond nodule, and muscle for radiomic feature extraction. Coefficient of variation (CV) within different ROIs and concordance correlation coefficient (CCC) between lung nodule and a given tissue region were calculated to test to determine feature uniqueness. The radiomic features were considered nonunique when (1) the CV < 10% and CCC > 0.85 for over 50% of patients; and (2) the CCC > 0.85 appeared in ≥2 tissue regions beyond the defined region.

resultsIn total, 14 patients from GE and 18 patients from Siemens are analyzed. The results show that 12 features fall below the 10% CV threshold for over 50% of patients in the GE cohort and 29 features in the Siemens cohort. According to CCC, 18 radiomic features in GE and 16 features in Siemens are identified as nonunique, with 11 overlapping features. Combining CV and CCC, 9 of 123 calculated features (7.3%) are identified as nonunique to a defined ROI.

conclusionsRadiomic feature uniqueness should be considered to improve the reliability of radiomics study.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsHumansReproducibility of ResultsRetrospective StudiesTomography, X-Ray Computedconcordance correlation coefficientfeature uniquenesslung cancerNSCLCradiomic features

Identifiers

PMID36173022
PMCPMC9797180

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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.