An <sup>18</sup>F-FDG PET/CT and Mean Lung Dose Model to Predict Early Radiation Pneumonitis in Stage III Non-Small Cell Lung Cancer Patients Treated with Chemoradiation and Immunotherapy.

Thor, Maria; Lee, Chen; Sun, Lian; Patel, Purvi; Apte, Aditya; Grkovski, Milan; Shepherd, Annemarie F; Gelblum, Daphna Y et al. · J Nucl Med · 2024

Where this comes from

Abstract

Radiation pneumonitis (RP) that develops early (i.e., within 3 mo) (RP<sub>Early</sub>) after completion of concurrent chemoradiation (cCRT) leads to treatment discontinuation and poorer survival for patients with stage III non-small cell lung cancer. Since no RP<sub>Early</sub> risk model exists, we explored whether published RP models and pretreatment <sup>18</sup>F-FDG PET/CT-derived features predict RP<sub>Early</sub> <b>Methods:</b> One hundred sixty patients with stage III non-small cell lung cancer treated with cCRT and consolidative immunotherapy were analyzed for RP<sub>Early</sub> Three published RP models that included the mean lung dose (MLD) and patient characteristics were examined. Pretreatment <sup>18</sup>F-FDG PET/CT normal-lung SUV featured included the following: 10th percentile of SUV (SUV<sub>P10</sub>), 90th percentile of SUV (SUV<sub>P90</sub>), SUV<sub>max</sub>, SUV<sub>mean</sub>, minimum SUV, and SD. Associations between models/features and RP<sub>Early</sub> were assessed using area under the receiver-operating characteristic curve (AUC), <i>P</i> values, and the Hosmer-Lemeshow test (pHL). The cohort was randomly split, with similar RP<sub>Early</sub> rates, into a 70%/30% derivation/internal validation subset. <b>Results:</b> Twenty (13%) patients developed RP<sub>Early</sub> Predictors for RP<sub>Early</sub> were MLD alone (AUC, 0.72; <i>P</i> = 0.02; pHL, 0.87), SUV<sub>P10</sub>, SUV<sub>P90,</sub> and SUV<sub>mean</sub> (AUC, 0.70-0.74; <i>P</i> = 0.003-0.006; pHL, 0.67-0.70). The combined MLD and SUV<sub>P90</sub> model generalized in the validation subset and was deemed the final RP<sub>Early</sub> model (RP<sub>Early</sub> risk = 1/[1+e<sup>(-</sup> <i><sup>x</sup></i> <sup>)</sup>]; <i>x</i> = -6.08 + [0.17 × MLD] + [1.63 × SUV<sub>P90</sub>]). The final model refitted in the 160 patients indicated improvement over the published MLD-alone model (AUC, 0.77 vs. 0.72; <i>P</i> = 0.0001 vs. 0.02; pHL, 0.65 vs. 0.87). <b>Conclusion:</b> Patients at risk for RP<sub>Early</sub> can be detected with high certainty by combining the normal lung's MLD and pretreatment <sup>18</sup>F-FDG PET/CT SUV<sub>P90</sub> This refined model can be used to identify patients at an elevated risk for premature immunotherapy discontinuation due to RP<sub>Early</sub> and could allow for interventions to improve treatment outcomes.

Medical subject headings