ArticleCancers2026
Multi-Institutional CT Scan-Based Radiomics for Predicting Tumor PD-L1 Expression in Patients with Advanced and Limited Non-Small Cell Lung Cancer.
Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
BACKGROUND/
objectivesImmune checkpoint inhibitors (ICIs) have revolutionized the treatment landscape of advanced non-small cell lung cancer (NSCLC), yet 70% of patients experience disease progression, underscoring the critical need for predictive biomarkers. Programmed death-ligand 1 (PD-L1) expression remains the most adopted biomarker for ICIs. With the emergence of machine learning, the development of radiomics algorithms based on CT scan images has demonstrated potential as a novel addition to the biomarker landscape in oncology. In this study, we aimed to develop a non-invasive surrogate of PD-L1 expression (rad-PDL1) derived from computed tomography (CT) scan imaging and compare its predictive value to pathological assessments. Furthermore, we evaluated its generalizability across advanced and limited-stage NSCLC.
methodsRadiomics features extracted from pretreatment CT were analyzed using a self-training pipeline that incorporated the feature tokenizer Transformer model to classify tumors as high vs. low PD-L1 expression. We included 482 advanced NSCLC patients treated with ICIs across three medical centers who were divided into training and hold-out validation sets. The algorithm was then further validated in an independent cohort of 51 patients with limited NSCLC treated with neoadjuvant ICI and chemotherapy.
resultsOur pipeline demonstrated strong predictive performance in primary and independent validation (AUC = 0.75 and 0.68, accuracy = 0.73 and 0.69, respectively), highlighting its generalizability and adaptability to various disease stages. Kaplan-Meier curves revealed a longer progression-free survival for patients in the high rad-PDL1.
conclusionsThese results demonstrate the feasibility of a CT-based radiomic surrogate of PD-L1 expression, showing partial generalization to an independent neoadjuvant cohort, while highlighting the need for larger prospective multi-site validation before clinical implementation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.