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AIM: The study aimed to evaluate whether there is any correlation between metabolic parameters derived from baseline fluorine-18 fluorodeoxyglucose (F-18 FDG) PET-computed tomography (CT) and programmed death-ligand 1 (PDL-1) expression in patients with metastatic non-small cell lung carcinoma (NSCLC). METHODS: 33 biopsy-proven metastatic NSCLC patients were included. On immunohistochemistry, a tumor proportion score (TPS) of ≥1% was considered PDL-1 positive, while a TPS of <1% was considered negative. Metabolic parameters of the F-18 FDG PET-CT scan were obtained by drawing a region of interest around the index lung lesion. Data were analyzed using Shapiro-Wilk test of normality, unpaired t-tests/Mann-Whitney U test, Spearman's rank correlation, Youden's index, and receiver operator characteristic (ROC) analysis. RESULTS: Spearman's correlation analysis demonstrated a moderate positive correlation (r = 0.466, P = 0.0063) between maximum standardized uptake value (SUVmax) and overall PDL-1 expression. Similarly, a moderate positive correlation was noted between SUVmax and tumors with positive PDL-1 expression (r = 0.643, P = 0.013), with mean SUVmax in PD-L1-positive tumors being significantly higher (P = 0.032). The ROC curve analysis yielded a cutoff value of SUVmax >18 to differentiate between PDL-1-positive and -negative tumors with a sensitivity of 57.1% and specificity of 89.5%. Total lesion glycolysis (TLG) and metabolic tumor volume (MTV) showed no significant association with PDL-1 expression (P = 0.58 and P = 0.88, respectively). CONCLUSION: The study indicates that SUVmax has the potential to be used as a noninvasive biomarker for predicting PDL-1 expression in NSCLC. No significant difference was noted in the median MTV and TLG values between the PDL-1-positive and -negative groups.
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Kumar et al. (2026) studied this question.
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