Evidence map›Paper›PMID 40688590›Full record

ArticleOncology letters2025

Predicting pathological staging of non-small cell lung cancer using a multi-task radiomics model integrating intratumoral and peritumoral features.

Ruonan Pan, Xiaoqian Lu, Xin Dong, Liang Guo, Xiang Li, Dianbo Cao

Abstract read
In one paragraph

Article in Oncology letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

6 authors.

Ruonan PanDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Xiaoqian LuDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Xin DongDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Liang GuoDepartment of Pathology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Xiang LiDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Dianbo CaoDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological staging is essential for guiding treatment decisions and determining prognosis in patients with non-small cell lung cancer (NSCLC). The present study aimed to establish a model using intratumoral and peritumoral features from computed tomography radiomics data and a multi-task learning algorithm, and evaluate its predictive performance for the pathological stage of NSCLC. Data from 198 eligible patients with NSCLC from The Cancer Imaging Archive database were retrospectively analyzed, which was used to develop four radiomics models to classify the pathological stages of NSCLC. These models combined the traditional random forest and multi-task random forest algorithms with the volumes of interest for the intratumoral region alone and with the intratumoral and peritumoral regions combined. Subsequently, the data from 90 patients from a real-world dataset were collected for use as an external test set. Diagnostic performance was evaluated using accuracy, precision, sensitivity, specificity, F1 scores and receiver operating characteristic curves. The results revealed that, in the internal test set, the area under the curve (AUC) values for model 1 (single-task model based on the intratumoral region), model 2 (single-task model combining intra- and peritumoral regions), model 3 (multi-task model based on the intratumoral region) and model 4 (multi-task model combining intra- and peritumoral regions) were 0.814, 0.900, 0.896 and 0.938, respectively. In the external test set, the AUC values were 0.821, 0.921, 0.858 and 0.939, separately. Moreover, the results of the DeLong test indicated that the AUC difference between model 1 and 4 was statistically significant (P<0.05). In conclusion, the multi-task radiomic model incorporating both intratumoral and peritumoral regions demonstrated favorable diagnostic efficacy in the predictive pathological staging of NSCLC.

Indexed as

intratumoral regionmulti-taskNSCLCpathological stagingperitumoral regionradiomics

Identifiers

PMID40688590
PMCPMC12273780

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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.