Exploratory evaluation of early (68)Ga-FAPI-46 PET/CT volume-based parameters in systemic sclerosis-associated interstitial lung disease

系统性硬化症相关间质性肺疾病早期(68)Ga-FAPI-46 PET/CT容积参数的探索性评估

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Abstract

PURPOSE: Systemic sclerosis-associated interstitial lung disease (SSc-ILD) is a severe complication of SSc, characterised by progressive fibrosis and inflammation. Current diagnostic tools do not accurately differentiate progressors from non-progressors, limiting timely intervention. (68)Ga-FAPI-46 is a positron emission tomography (PET) tracer targeting fibroblast activation protein alpha (FAP), a marker of activated fibroblasts, with high affinity and retention. Optimal imaging timepoints and PET parameters for (68)Ga-FAPI-46 PET/CT imaging in fibroinflammatory disorders remain undefined. This exploratory study investigated early versus late (68)Ga-FAPI-46 PET parameters in evaluating SSc-ILD. METHODS: Early (10 min) and late (60 min) (68)Ga-FAPI-46 PET parameters were compared between progressive (n = 8) and non-progressive SSc-ILD (n = 14), defined by INBUILD trial criteria. PET parameters were correlated with pulmonary function test (PFT) and HRCT parameters. Optimal thresholds for identified PET parameters were determined by closest-to-(0,1) criterion. RESULTS: Early total lesion FAPI uptake (median TL-FAPI(10min) 1245 vs. 714, p = 0.020) and affected lung volume (median AV(10min) 514 ml vs. 368 ml, p = 0.042) were significantly higher in progressors than non-progressors. Early PET parameters showed stronger, more consistent correlations with PFT and quantitative HRCT parameters than late PET parameters. Volume-based compared to intensity-based PET parameters more consistently correlated with PFT and quantitative HRCT parameters. TL-FAPI(10min) threshold of 928 had the best diagnostic performance (AUC 0.80). CONCLUSION: This exploratory study showed that (68)Ga-FAPI-46 PET/CT imaging, specifically early volume-based PET parameters, was associated with patients with recent disease progression of SSc-ILD. Prospective validation in treatment-response studies is needed to confirm the clinical utility of these PET parameters and their identified preliminary thresholds.

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