Evidence map›Paper›PMID 36047542›Full record

ArticleKorean journal of radiology2022

Combination of

Shen Li, Yadi Li, Min Zhao, Pengyuan Wang, Jun Xin

Abstract read
In one paragraph

Article in Korean journal of radiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 3 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

18 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Predictive value ofFrontiers in oncology · 2024
    Pooled it
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. ExplainableJournal of cancer research and clinical oncology · 2024
    Article
  10. New Oncologic Imaging Section in theKorean journal of radiology · 2024
    Article
  11. Article
  12. Review
  13. The predictive value of [EJNMMI research · 2023
    Article
  14. Article
  15. Prediction of EGFR mutation status in lung adenocarcinoma based onAmerican journal of nuclear medicine and molecular imaging · 2023
    Article
  16. Review
  17. OptimalFrontiers in oncology · 2023
    Article
  18. 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

5 authors.

Shen LiDepartment of Radiology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID 0000-0003-1530-5221
Yadi LiDepartment of Radiology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID 0000-0001-9473-8839
Min ZhaoPharmaceutical Diagnostics, GE Healthcare, Beijing, China.ORCID 0000-0002-7154-8415
Pengyuan WangDepartment of Radiology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID 0000-0003-2441-1384
Jun XinDepartment of Radiology, Shengjing Hospital of China Medical University, Shenyang, China. xinj@sj-hospital.org.ORCID 0000-0001-5660-6368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo identify epidermal growth factor receptor (EGFR) mutations in lung adenocarcinoma based on MATERIALS AND

methodsWe retrospectively analyzed 179 patients with lung adenocarcinoma. They were randomly assigned to training (n = 125) and testing (n = 54) cohorts in a 7:3 ratio. A total of 2632 radiomics features were extracted from the tumor region of interest from the PET (1316) and CT (1316) images. Six PET/CT radiomics features that remained after the feature selection step were used to calculate the radiomics model score (rad-score). Subsequently, a combined clinical and radiomics model was constructed based on sex, smoking history, tumor diameter, and rad-score. The performance of the combined model in identifying EGFR mutations was assessed using a receiver operating characteristic (ROC) curve. Furthermore, in a subsample of 99 patients, a PET/CT radiomics model for distinguishing 19 del and 21 L858R EGFR mutational subtypes was established, and its performance was evaluated.

resultsThe area under the ROC curve (AUROC) and accuracy of the combined clinical and PET/CT radiomics models were 0.882 and 81.6%, respectively, in the training cohort and 0.837 and 74.1%, respectively, in the testing cohort. The AUROC and accuracy of the radiomics model for distinguishing between 19 del and 21 L858R EGFR mutational subtypes were 0.708 and 66.7%, respectively, in the training cohort and 0.652 and 56.7%, respectively, in the testing cohort.

conclusionThe combined clinical and PET/CT radiomics model could identify the EGFR mutational status in lung adenocarcinoma with moderate accuracy. However, distinguishing between EGFR 19 del and 21 L858R mutational subtypes was more challenging using PET/CT radiomics.

Indexed as

Adenocarcinoma of LungLung NeoplasmsErbB ReceptorsFluorodeoxyglucose F18HumansMutationPositron Emission Tomography Computed TomographyRetrospective StudiesErbB ReceptorsFluorodeoxyglucose F18Epidermal growth factor receptorLung adenocarcinomaPET/CTPredictionRadiomics

Identifiers

PMID36047542
PMCPMC9434738

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.