Evidence map›Paper›PMID 35422977›Full record

ArticleJournal of healthcare engineering2022

Establishment and Evaluation of EGFR Mutation Prediction Model Based on Tumor Markers and CT Features in NSCLC.

Hao Zhang, Meng He, Ren'an Wan, Liangming Zhu, Xiangpeng Chu

Open access · hybridAbstract read
In one paragraph

Article in Journal of healthcare engineering, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Advances in laboratory medicine · 2025
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  2. Integrating ctDNA testing forAdvances in laboratory medicine · 2025
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  3. MVASA-HGN: multi-view adaptive semantic-aware heterogeneous graph network forQuantitative imaging in medicine and surgery · 2025
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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

5 authors at 2 institutions in 1 country.

Hao ZhangDepartment of Thoracic Surgery, Rizhao People's Hospital, Rizhao 276800, Shandong, China.
Meng HeDepartment of Thoracic Surgery, Rizhao People's Hospital, Rizhao 276800, Shandong, China.
Ren'an WanDepartment of Thoracic Surgery, Rizhao People's Hospital, Rizhao 276800, Shandong, China.
Liangming ZhuDepartment of Thoracic Surgery, Jinan Central Hospital, Jinan 250013, Shandong, China.
Xiangpeng ChuDepartment of Thoracic Surgery, Rizhao People's Hospital, Rizhao 276800, Shandong, China.ORCID 0000-0001-7164-9067
People’s Hospital of Rizhao · CNJinan Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lung cancer has become one of the leading causes of cancer deaths worldwide. EGFR gene mutation has been reported in up to 60% of Asian populations and is currently one of the main targets for genotype-targeted therapy for NSCLC. Objective: The objective is to determine if a complex model combining serum tumor makers and computed tomographic (CT) features can predict epidermal growth factor receptor (EGFR) mutation with higher accuracy. Results: Logistic regression analysis identified the predictive factors of EGFR mutation including nonsmoking, high expression level of Carcinoembryonic Antigen (CEA), low expression level of cytokeratin 19 fragments (CYFRA21-1), and subsolid density containing ground-glass opacity (GGO) component. Using the results of multivariate logistic regression analysis, we built a statistically determined clinical prediction model. The AUC of the complex prediction model increased significantly from 0.735 to 0.813 ( Conclusion: A complex model combining serum tumor makers and CT features is more accurate in predicting EGFR mutation status in NSCLC patients than using either serum variables or imaging features alone. Our finding for EGFR mutation is urgently needed and helpful in clinical practice.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntigens, NeoplasmBiomarkers, TumorErbB ReceptorsHumansKeratin-19Models, StatisticalMutationPrognosisRetrospective StudiesTomography, X-Ray Computedantigen CYFRA21.1Antigens, NeoplasmBiomarkers, TumorEGFR protein, humanErbB ReceptorsKeratin-19

Identifiers

PMID35422977
PMCPMC9005305
OpenAlexW4226156883

What OpenQuestion holds

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LicenceCC BY
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.