ArticleScientific reports2026
Deep learning and radiomics models in patients with advanced non-small cell lung cancer treated with immunotherapy combined with stereotactic radiotherapy.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.
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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.
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.
Phase I/II Trial of MK-3475 and Hypofractionated Stereotactic Radiation Therapy in Patients With NSCLC
Randomized Phase II, 2-arm Study of Pembrolizumab After High Dose Radiation (SBRT) Versus Pembrolizumab Alone in Patients With Advanced Non-small Cell Lung Cancer
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Authors and funding
14 authors.
Funding
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Abstract
Quantitative imaging is an emerging field that may allow prediction of oncological outcomes. We investigate whether radiomics and deep learning can predict outcomes in metastatic non-small cell lung cancer utilizing randomized trials of PD-1 inhibitors + /- stereotactic ablative body radiotherapy: PEMBRO-RT(NCT02492568), NIVORAD(ACTRN12616000352404) and MDACC(NCT02444741). A random forest model developed on PEMBRO-RT using radiomics features had an AUC of 0.57 for prediction of per-lesion progressive disease on immunotherapy compared to an AUC of 0.92 for a deep learning model. A random forest survival model using radiomics features for overall survival (progression free survival) had a concordance index of 0.63(0.59) and improved to 0.67(0.65) by adding clinical features, including PD-L1 and treatment arm. Validation on NIVORAD and MDACC revealed reduced AUCs. Overall, a deep learning compared to a radiomics model demonstrated excellent predictive value for per-lesion progressive disease for patients on immunotherapy. Models had reduced performance on external validation. Research improving generalizability is required for clinical translation.
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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.