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e20613 Background: Accurate prediction of how patients with non-small cell lung cancer (NSCLC) will respond to immunotherapy is essential for customizing individual treatment plans. This research explores the use of radiomics analysis from pre-treatment CT scans as a method to predict the effectiveness of immunotherapy in individuals with NSCLC. Methods: This IRB-approved retrospective study investigated radiologic and clinical data from 159 patients with stage III-IV NSCLC treated with immunotherapy. Imaging responses were assessed according to RECIST 1.1 and immune-related RECIST (irRECIST) criteria at least twice during a 24-week period. Responses were categorized as complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD). 3D radiomics features were extracted from both the tumor and a 1 cm thick peritumoral region. A linear mixed-effect harmonization model was employed to correct for scanner-associated variations. A Random Forest algorithm was used to develop a classification model to predict response according to RECIST 1.1 or irRECIST. The dataset was split into training (70%) and test (30%) sets. The accuracy of predictions was evaluated using confusion matrix statistics and bootstrapping with 1,000 iterations for median and 95% confidence interval (CI). Results: Using RECIST 1.1 criteria, 41 patients (25.2%) achieved PR and CR(0.6), 62 (39.0%) achieved SD, and 56 (35.2%) achieved PD. IrRECIST criteria yielded slightly higher CR/PR rates with 52 patients (32.7%), while SD decreased to 65 (41.0%) and PD remained at 42 (26.4%). For predicting CR/PR and SD responses, the models achieved a sensitivity of 0.45 (95% CI: 0.38-0.50) and 0.64 (0.60-0.68) for irRECIST, compared to 0.34 (0.28-0.38) and 0.55 (0.52-0.60) for RECIST 1.1. The corresponding specificity was 0.85 (0.83-0.87) and 0.63 (0.59-0.67) for irRECIST, compared to 0.91 (0.89-0.93) and 0.67 (0.63-0.72) for RECIST 1.1. For predicting PD response, the models achieved a sensitivity of 0.49 (0.45-0.56) for irRECIST and 0.57 (0.52-0.62) for RECIST 1.1. The models' balanced accuracy for predicting CR/PR, SD, and PD were 0.65 (0.61-0.68), 0.64 (0.61-0.67), and 0.65 (0.63-0.69) for irRECIST, compared to 0.62 (0.59-0.64), 0.61 (0.59-0.64), and 0.62 (0.59-0.64) for RECIST 1.1, respectively. Conclusions: This study demonstrates the potential of pre-treatment CT radiomics to predict immunotherapy responses in NSCLC patients, offering insights into personalized treatment approaches. However, larger studies are needed to validate our findings.
Yadav et al. (Sat,) studied this question.
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