Evidence map›Paper›PMID 32096372›Full record

ArticleSheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi2020

[Prediction of gene mutation in lung cancer based on deep learning and histomorphology analysis].

Quan Wang, Qin Shen, Zelin Zhang, Chengfei Cai, Haoda Lu, Xiaojun Zhou, Jun Xu

Open access · greenAbstract read
In one paragraph

Article in Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 21% of its field
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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. [Research on deep learning-based pathological image classification of pilonidal sinus].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. [Deep learning-based fully automated intelligent and precise diagnosis for melanocytic lesions].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2022
    Article
  6. Article
  7. Review
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

7 authors at 2 institutions in 1 country.

Quan WangSchool of Automation, Nanjing University of Information Science and Technology, Nanjing 210044, P.R.China;Jiangsu Key Laboratory of Large Data Analysis Technology, Nanjing 210044, P.R.China.
Qin ShenDepartment of Pathology, Nanjing General Hospital, Nanjing 210002, P.R.China.
Zelin ZhangSchool of Automation, Nanjing University of Information Science and Technology, Nanjing 210044, P.R.China;Jiangsu Key Laboratory of Large Data Analysis Technology, Nanjing 210044, P.R.China.
Chengfei CaiSchool of Automation, Nanjing University of Information Science and Technology, Nanjing 210044, P.R.China;Jiangsu Key Laboratory of Large Data Analysis Technology, Nanjing 210044, P.R.China.
Haoda LuSchool of Automation, Nanjing University of Information Science and Technology, Nanjing 210044, P.R.China;Jiangsu Key Laboratory of Large Data Analysis Technology, Nanjing 210044, P.R.China.
Xiaojun ZhouDepartment of Pathology, Nanjing General Hospital, Nanjing 210002, P.R.China.
Jun XuSchool of Automation, Nanjing University of Information Science and Technology, Nanjing 210044, P.R.China;Jiangsu Key Laboratory of Large Data Analysis Technology, Nanjing 210044, P.R.China.
Nanjing University of Information Science and Technology · CNNanjing General Hospital of Nanjing Military Command · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is a most common malignant tumor of the lung and is the cancer with the highest morbidity and mortality worldwide. For patients with advanced non-small cell lung cancer who have undergone epidermal growth factor receptor (EGFR) gene mutations, targeted drugs can be used for targeted therapy. There are many methods for detecting EGFR gene mutations, but each method has its own advantages and disadvantages. This study aims to predict the risk of EGFR gene mutation by exploring the association between the histological features of the whole slides pathology of non-small cell lung cancer hematoxylin-eosin (HE) staining and the patient's EGFR mutant gene. The experimental results show that the area under the curve (AUC) of the EGFR gene mutation risk prediction model proposed in this paper reached 72.4% on the test set, and the accuracy rate was 70.8%, which reveals the close relationship between histomorphological features and EGFR gene mutations in the whole slides pathological images of non-small cell lung cancer. In this paper, the molecular phenotypes were analyzed from the scale of the whole slides pathological images, and the combination of pathology and molecular omics was used to establish the EGFR gene mutation risk prediction model, revealing the correlation between the whole slides pathological images and EGFR gene mutation risk. It could provide a promising research direction for this field.

Indexed as

Deep LearningCarcinoma, Non-Small-Cell LungErbB ReceptorsHumansLung NeoplasmsMutationEGFR protein, humanErbB Receptorsdeep learninggene mutationhistopathological imagelung cancerprecision medicine

Identifiers

PMID32096372
PMCPMC9927658
OpenAlexW3012945969

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.