The Proliferation Saturation Index (PSI) model is a patient-specific mathematical model designed to simulate and predict tumour volume regression (TVR) during radiation therapy (RT) using early treatment response dynamics. This study validates the PSI model in an independent external cohort of patients with non-small cell lung cancer (NSCLC) using previously derived model parameters. In a cohort of 71 patients, treated with definitive RT alone (55Gy/20#) tumour volume measurements extracted from 6 Cone Beam CT (CBCT) scans acquired on days 1, 2 and 3 and weekly thereafter. Model predictions of TVR at final CBCT (CBCT6) were made using tumour volume dynamics recorded from CBCT 1-3, CBCT 1-4 and CBCT 1-5. Agreement between predicted and actual volumes were assessed using the coefficient of Determination (R²) and Pearson Correlation Coefficient (PCC). Model predictions showed strong agreement with measured volumes, improving with additional input data: R² increased from 0.81 (3 inputs) to 0.94 (5 inputs), and PCC rose from 0.90 to 0.97. Prediction using data from approximately Day 10 of RT (CBCT4) yielded R² = 0.91 and PCC = 0.95. The model demonstrated strong performance in identifying poor responders (TVR ≤10%) with sensitivity of 77.7%, specificity of 73.6%, and a negative predictive value of 90.7%. Sensitivity analysis confirmed model stability with under ±20% parameter variation. This external validation confirms the PSI model’s reproducibility and robustness in predicting TVR in NSCLC patients treated with definitive RT, supporting its integration into personalised RT planning strategies.
Barrett et al. (Sun,) studied this question.