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Peer-reviewedCC BYFrontiers in immunology

Clinical variables and quantitative CT radiomics for mortality risk stratification after acute exacerbation of idiopathic inflammatory myopathy-associated interstitial lung disease

  1. 1Department of Radiology, The First Affiliated Hospital of Xi’an Jiaotong University , ,

Abstract

Background: Acute exacerbation (AE) is the most lethal event of idiopathic inflammatory myopathy-associated interstitial lung disease (IIM-ILD). This exploratory study compared clinical, radiomics, and combined predictor strategies across five survival-learning algorithms for survival risk stratification.

Methods: We retrospectively analyzed 78 patients with AE-IIM-ILD and divided them into a training cohort (n = 54; 20 deaths) and a held-out internal testing cohort (n = 24; 9 deaths), stratified by observed mortality event status. Three predictor strategies were evaluated: a clinical strategy comprising PaO ₂ /FiO ₂ ratio, neutrophil percentage (NEU%), and arthritis-related symptoms; a radiomics strategy comprising two selected radiomics features; and a combined strategy comprising PaO ₂ /FiO ₂ ratio, arthritis-related symptoms, and a composite radiomics score (Rad-score). Each strategy was evaluated using five survival-learning algorithms. Harrell’s concordance index (C-index) was the primary discrimination metric, with mean time-dependent area under the curve (AUC) used as a secondary measure.

Results: During the 1-year follow-up, 29 deaths were observed. Performance rankings varied across predictor strategies, algorithms, and evaluation metrics. The combined-Random Survival Forest configuration demonstrated the highest training-cohort C-index among the 15 configurations. Its mean time-dependent AUC was 0.923 (95% CI: 0.860–0.970) in the training cohort and 0.915 (95% CI: 0.736–0.986) in the testing cohort, with corresponding C-indices of 0.874 (95% CI: 0.803–0.940) and 0.842 (95% CI: 0.673–0.971), respectively. The model stratified patients into high- and low-risk groups with distinct observed survival trajectories.

Conclusion: In this exploratory cohort, integrating selected clinical variables with a quantitative CT Rad-score using RSF showed promising numerical discrimination and risk-stratification performance. These findings suggest that clinical and quantitative imaging information may provide complementary prognostic information after AE-IIM-ILD.

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BibTeX
@article{he2026clinical,
  title = {{Clinical variables and quantitative CT radiomics for mortality risk stratification after acute exacerbation of idiopathic inflammatory myopathy-associated interstitial lung disease}},
  author = {Liyu He and Yanrong Chen and Jingping Zhang and Kai Yang and Shuo Yu and Yaqi Yan and Yuhan Bian and Youmin Guo and Chenwang Jin},
  journal = {Frontiers in immunology},
  year = {2026},
  month = oct,
  doi = {10.3389/fimmu.2026.1917500},
  url = {https://europepmc.org/article/PMC/PMC13672662},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Clinical variables and quantitative CT radiomics for mortality risk stratification after acute exacerbation of idiopathic inflammatory myopathy-associated interstitial lung disease
AU  - Liyu He
AU  - Yanrong Chen
AU  - Jingping Zhang
AU  - Kai Yang
AU  - Shuo Yu
AU  - Yaqi Yan
AU  - Yuhan Bian
AU  - Youmin Guo
AU  - Chenwang Jin
PY  - 2026
DA  - 2026/10/02
JO  - Frontiers in immunology
DO  - 10.3389/fimmu.2026.1917500
UR  - https://europepmc.org/article/PMC/PMC13672662
AB  - Background: Acute exacerbation (AE) is the most lethal event of idiopathic inflammatory myopathy-associated interstitial lung disease (IIM-ILD). This exploratory study compared clinical, radiomics, and combined predictor strategies across five survival-learning algorithms for survival risk stratification.  Methods: We retrospectively analyzed 78 patients with AE-IIM-ILD and divided them into a training cohort (n = 54; 20 deaths) and a held-out internal testing cohort (n = 24; 9 deaths), stratified by observed mortality event status. Three predictor strategies were evaluated: a clinical strategy comprising PaO ₂ /FiO ₂ ratio, neutrophil percentage (NEU%), and arthritis-related symptoms; a radiomics strategy comprising two selected radiomics features; and a combined strategy comprising PaO ₂ /FiO ₂ ratio, arthritis-related symptoms, and a composite radiomics score (Rad-score). Each strategy was evaluated using five survival-learning algorithms. Harrell’s concordance index (C-index) was the primary discrimination metric, with mean time-dependent area under the curve (AUC) used as a secondary measure.  Results: During the 1-year follow-up, 29 deaths were observed. Performance rankings varied across predictor strategies, algorithms, and evaluation metrics. The combined-Random Survival Forest configuration demonstrated the highest training-cohort C-index among the 15 configurations. Its mean time-dependent AUC was 0.923 (95% CI: 0.860–0.970) in the training cohort and 0.915 (95% CI: 0.736–0.986) in the testing cohort, with corresponding C-indices of 0.874 (95% CI: 0.803–0.940) and 0.842 (95% CI: 0.673–0.971), respectively. The model stratified patients into high- and low-risk groups with distinct observed survival trajectories.  Conclusion: In this exploratory cohort, integrating selected clinical variables with a quantitative CT Rad-score using RSF showed promising numerical discrimination and risk-stratification performance. These findings suggest that clinical and quantitative imaging information may provide complementary prognostic information after AE-IIM-ILD.
SN  - 1664-3224
ER  -