Radiomics and Delta-Radiomics Signatures to Predict Response and Survival in Patients with Non-Small-Cell Lung Cancer Treated with Immune Checkpoint Inhibitors.
François CousinThomas LouisSophie DheurFrank Aboubakar NanaBenoit GhayeMariaelena OcchipintiWim VosFabio BottariAstrid PaulusAnne SibilleFrédérique VaillantBernard DuysinxJulien GuiotRoland HustinxPublished in: Cancers (2023)
The aim of our study was to determine the potential role of CT-based radiomics in predicting treatment response and survival in patients with advanced NSCLC treated with immune checkpoint inhibitors. We retrospectively included 188 patients with NSCLC treated with PD-1/PD-L1 inhibitors from two independent centers. Radiomics analysis was performed on pre-treatment contrast-enhanced CT. A delta-radiomics analysis was also conducted on a subset of 160 patients who underwent a follow-up contrast-enhanced CT after 2 to 4 treatment cycles. Linear and random forest (RF) models were tested to predict response at 6 months and overall survival. Models based on clinical parameters only and combined clinical and radiomics models were also tested and compared to the radiomics and delta-radiomics models. The RF delta-radiomics model showed the best performance for response prediction with an AUC of 0.8 (95% CI: 0.65-0.95) on the external test dataset. The Cox regression delta-radiomics model was the most accurate at predicting survival with a concordance index of 0.68 (95% CI: 0.56-0.80) ( p = 0.02). The baseline CT radiomics signatures did not show any significant results for treatment response prediction or survival. In conclusion, our results demonstrated the ability of a CT-based delta-radiomics signature to identify early on patients with NSCLC who were more likely to benefit from immunotherapy.
Keyphrases
- contrast enhanced
- diffusion weighted
- magnetic resonance imaging
- magnetic resonance
- computed tomography
- diffusion weighted imaging
- dual energy
- small cell lung cancer
- lymph node metastasis
- newly diagnosed
- squamous cell carcinoma
- free survival
- dna methylation
- end stage renal disease
- combination therapy
- advanced non small cell lung cancer
- climate change
- genome wide