Evidence map›Paper›PMID 42375379›Full record

ArticleFrontiers in immunology2026

Comparative evaluation of machine learning models for predicting PD-L1 high expression in resectable NSCLC: a dual-center study integrating [

Jiong Lin, Xin Li, Jiming Tang, Haijie Xu, Xirui Lin, Chaoquan He, Peishen Li, Jiayin Wu, Weixing Huang, Hansheng Wu

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jiong LinDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Xin LiShantou University Medical College, Shantou, China.
Jiming TangDepartment of Thoracic Surgery, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China.
Haijie XuDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Xirui LinDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Chaoquan HeDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Peishen LiDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Jiayin WuDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Weixing HuangJoint Cardiac Surgery Center, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.
Hansheng WuDepartment of Thoracic Surgery, The First Affiliated Hospital of Shantou University Medical College, Shantou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Accurate prediction of programmed death-ligand 1 (PD-L1) high expression (tumor proportion score [TPS] ≥50%) is important for identifying patients with resectable non-small cell lung cancer (NSCLC) who may benefit from neoadjuvant chemoimmunotherapy (nCIT). This study aimed to evaluate eight machine learning (ML) algorithms and develop a non-invasive, [ Methods: A retrospective, dual-center cohort of 269 patients with stage IB-IIIB resectable NSCLC who underwent [ Results: Of the 269 enrolled patients, 79.9% were male and 32.0% were older than 65 years. LASSO regression identified five core predictors: smoking status, histological type, T stage, histological grade, and SUVmax. In the independent external validation set, Support Vector Machine (SVM) (AUC = 0.858), Random Forest (RF) (AUC = 0.849), and Logistic Regression (LR) (AUC = 0.833) demonstrated good discriminative performance. However, DeLong's test indicated no statistically significant advantage of the complex models over the traditional LR model (all adjusted P = 1.000). Prioritizing model transparency and interpretability, an LR-based nomogram was established, which exhibited favorable calibration and provided clinical net benefit across a wide range of threshold probabilities in both cohorts. Conclusions: We developed and validated an interpretable, [

Indexed as

B7-H1 AntigenCarcinoma, Non-Small-Cell LungLung NeoplasmsMachine LearningPositron Emission Tomography Computed TomographyAgedClassification AlgorithmsFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedNeoplasm StagingPrediction AlgorithmsPredictive Learning ModelsRadiopharmaceuticalsB7-H1 AntigenCD274 protein, humanFluorodeoxyglucose F18Radiopharmaceuticalsmachine learningneoadjuvant chemoimmunotherapynomogramnon-small cell lung cancerPD-L1PET/CT

Identifiers

PMID42375379
PMCPMC13311110

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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.