Evidence map›Paper›PMID 37095981›Full record

ArticleHeliyon2023

Deep learning-powered 3D segmentation derives factors associated with lymphovascular invasion and prognosis in clinical T1 stage non-small cell lung cancer.

Zhichao Zuo, Xiaohong Fan, Yao Tang, Yang Zhang, Xin Peng, Weihua Zeng, Ying Zeng

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Zhichao ZuoDepartment of Radiology, Xiangtan Central Hospital, Xiangtan, Hunan, 411000, China.
Xiaohong FanThe School of Mathematics and Computational Science, Xiangtan University, Xiangtan, Hunan, 411105, China.
Yao TangDepartment of Pathology, Xiangtan Central Hospital, Xiangtan, Hunan, 411000, China.
Yang ZhangDepartment of Pathology, Xiangtan Central Hospital, Xiangtan, Hunan, 411000, China.
Xin PengDepartment of Radiology, Xiangtan Central Hospital, Xiangtan, Hunan, 411000, China.
Weihua ZengDepartment of Radiology, Xiangtan Central Hospital, Xiangtan, Hunan, 411000, China.
Ying ZengDepartment of Radiology, Xiangtan Central Hospital, Xiangtan, Hunan, 411000, China.
Xiangyang Central Hospital · CNXiangtan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lymphovascular invasion (LVI) is an invasive biologic behavior that affects the treatment and prognosis of patients with early-stage lung cancer. This study aimed to identify LVI diagnostic and prognostic biomarkers using deep learning-powered 3D segmentation with artificial intelligence (AI) technology. Methods: Between January 2016 and October 2021, we enrolled patients with clinical T1 stage non-small cell lung cancer (NSCLC). We used commercially available AI software (Dr. Wise system, Deep-wise Corporation, China) to extract quantitative AI features of pulmonary nodules automatically. Dimensionality reduction was achieved through least absolute shrinkage and selection operator regression; subsequently, the AI score was calculated.Then, the univariate and multivariate analysis was further performed on the AI score and patient baseline parameters. Results: Among 175 enrolled patients, 22 tested positive for LVI at pathology review. Based on the multivariate logistic regression results, we incorporated the AI score, carcinoembryonic antigen, spiculation, and pleural indentation into the nomogram for predicting LVI. The nomogram showed good discrimination (C-index = 0.915 [95% confidence interval: 0.89-0.94]); moreover, calibration of the nomogram revealed good predictive ability (Brier score = 0.072). Kaplan-Meier analysis revealed that relapse-free survival and overall survival were significantly higher among patients with a low-risk AI score and without LVI than those among patients with a high-risk AI score (p = 0.008 and p = 0.002, respectively) and with LVI (p = 0.013 and p = 0.008, respectively). Conclusions: Our findings indicate that a high-risk AI score is a diagnostic biomarker for LVI in patients with clinical T1 stage NSCLC; accordingly, it can serve as a prognostic biomarker for these patients.

Indexed as

3D segmentationArtificial intelligenceClinical T1 stage non-small cell lung cancerDeep learningLymphovascular invasion

Identifiers

PMID37095981
PMCPMC10121934
OpenAlexW4362584373

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Registered trials

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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.