# Fusing data from CT deep learning, CT radiomics and peripheral blood immune profiles to diagnose lung cancer in a cohort of patients experiencing symptoms

**Authors:** Rami Mustapha, Balaji Ganeshan, Sam Ellis, Luigi Dolcetti, Mukunthan Tharmakulasingam, Karen DeSouza, Xiaolan Jiang, Courtney Savage, Sheena Lim, Emily Chan, Andrew Thornton, Luke Hoy, Raymond Endozo, Rob Shortman, Darren Walls, Shih-Hsin Chen, Mark Rowley, Anthony C.C. Coolen, Ashley M. Groves, Julia A. Schnabel, Thida Win, Paul R. Barber, Tony Ng

PMC · DOI: 10.1016/j.ebiom.2026.106173 · eBioMedicine · 2026-02-19

## TL;DR

This study combines CT scan data and blood immune profiles to improve lung cancer diagnosis in symptomatic patients.

## Contribution

A novel diagnostic approach fusing CT deep learning, radiomics, and immune profiles to enhance lung cancer detection.

## Key findings

- Single modality signatures achieved AUCs of 0.69 (immune), 0.70 (CTTA), and 0.73 (DLA).
- The combined signature achieved a higher ROC AUC of 0.81 with 72% sensitivity and 77% specificity.
- Fusing immune and CT data improves diagnostic accuracy for lung cancer in symptomatic patients.

## Abstract

Lung cancer is the leading cause of cancer-related deaths. Diagnosis at late stages is common due to the largely non-specific nature of presenting symptoms contributing to high mortality. There is a lack of specific, minimally invasive low-cost tests to screen patients ahead of the diagnostic biopsy.

344 patients experiencing symptoms from the lung clinic of Lister hospital suspected of lung cancer were recruited. Predictive covariates were successfully generated on 170 patients from Computed Tomography (CT) scans using CT Texture Analysis (CTTA) and Deep Learning Autoencoders (DLA) as well as from peripheral blood data for immunity using high depth flow-cytometry and for exosome protein components. Predictive signatures were formed by combining covariates using Bayesian regression on a randomly chosen 128-patient training set and validated on a 42-patient held-out set. Final signatures were generated by fusing the data sources at different levels.

Immune, CTTA and DLA single modality signatures had overall AUCs of 0.69, 0.70 and 0.73 respectively. The final combined signature had a ROC AUC of 0.81. The overall sensitivity and specificity were 0.72 and 0.77 respectively.

Combining immune monitoring with CT scan data is an effective approach to improving sensitivity and specificity of Lung cancer screening even in patients experiencing symptoms.

CRUK [C1519/A27375], 10.13039/100010269Wellcome Trust/EPSRC Centre for Medical Engineering [WT203148/Z/16/Z], NIHR Clinical Research Facility at 10.13039/501100004941Guy's and St Thomas' NHS Foundation Trust, NIHR Biomedical Research Centre.

## Linked entities

- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, LAMP1 (lysosome associated membrane protein 1) [NCBI Gene 3916] {aka CD107a, LAMPA, LGP120}, CDK1 (cyclin dependent kinase 1) [NCBI Gene 983] {aka CDC2, CDC28A, P34CDC2}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, KLRA1P (killer cell lectin like receptor A1, pseudogene) [NCBI Gene 10748] {aka KLRA1, KLRAP1, LY49L, Ly-49L, Ly49}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, KIR3DL1 (killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1) [NCBI Gene 3811] {aka CD158E1, KIR, KIR3DL1/S1, NKAT-3, NKAT3, NKB1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 80380] {aka B7DC, Btdc, CD273, PD-L2, PDCD1L2, PDL2}
- **Diseases:** Hypoxia (MESH:D000860), non (MESH:C580335), lupus (MESH:D008180), celiac disease (MESH:D002446), tumorigenesis (MESH:D063646), DLA (MESH:D007859), lesion (MESH:D009059), head and neck cancer (MESH:D006258), Cancer (MESH:D009369), Lung (MESH:D008171), Lung Cancer (MESH:D008175), prostate cancer (MESH:D011471), melanoma (MESH:D008545), inflammation (MESH:D007249), renal cell carcinoma (MESH:D002292), HIV (MESH:D015658), allergic reaction (MESH:D004342), breast cancer (MESH:D001943), LDCT (MESH:C000719218), infection (MESH:D007239), CRC (MESH:D015179), death (MESH:D003643), metastasis (MESH:D009362)
- **Chemicals:** lactate (MESH:D019344), 18 F-fluorodeoxyglucose (MESH:D019788), A27375 (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12936772/full.md

## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936772/full.md

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Source: https://tomesphere.com/paper/PMC12936772