Predicting [90Y]Y-FAPI-46 Tumor Absorbed Dose from Single-Time-Point [68Ga]Ga-FAPI-46 PET/CT Imaging.

IF 9.1
Masao Watanabe, Walter Jentzen, Ken Herrmann, David Kersting, Pedro Fragoso Costa
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Abstract

Radiolabeled fibroblast activation protein (FAP)-targeting peptides, such as 90Y-FAPI-46, have increasingly been used to treat various tumor entities, with preliminary reports indicating therapeutic responses with acceptable toxicity profiles. Dosimetry can be used to maximize antitumor capability and minimize side effects. The aim of this study was to investigate whether 90Y-FAPI-46 tumor dosimetry can be predicted by diagnostic 68Ga-FAPI-46 PET/CT data. Methods: Fourteen patients with 24 lesions underwent a single-time-point 68Ga-FAPI-46 PET/CT scan and 3 90Y-FAPI-46 PET/CT scans for dosimetry within a 3-mo interval. Tumors were identified on PET images, and the anatomic tumor volume was measured on low-dose CT. Tumor uptake extrapolated at time of injection, time-integrated activity coefficient (TIAC), and tumor absorbed dose were calculated as reference values using 90Y-FAPI-46 data and compared with the corresponding predicted values using 68Ga-FAPI-46 data by means of a single-time-point dosimetry model. Correlations between 90Y-FAPI-46- and 68Ga-FAPI-46-based values were assessed. Results: In calculating the predicted values using a single-time-point 68Ga-FAPI-46 PET/CT, the mean effective half-life of 90Y-FAPI-46 across all lesions was 8.44 ± 1.73 h. The mean ± SD ratio (i.e., the predicted values using 68Ga-FAPI-46 data divided by the reference 90Y-FAPI-46 data) were 0.93 ± 0.39, 0.77 ± 0.35, and 0.77 ± 0.35 for tumor uptake, TIAC, and tumor absorbed dose, respectively. In the Bland-Altman analysis, mean differences (bias) ± SD of the percent differences of tumor uptake, TIAC, and tumor absorbed dose were -16.11% ± 43.28% (95% CI, -100.90 to 68.73%; Spearman ρ = 0.91; P < 0.0001), -32.60% ± 41.26% (95% CI, -113.50 to 48.26%; Spearman ρ = 0.91; P < 0.0001), and -33.35% ± 40.19% (95% CI, -112.10 to 45.43%; Spearman ρ = 0.77; P < 0.0001), respectively. Conclusion: Tumor uptake, TIAC, and tumor absorbed dose on 90Y-FAPI-46 PET/CT and 68Ga-FAPI-46 PET/CT were highly correlated, although the values on 68Ga-FAPI-46 PET/CT tended to be lower than those on 90Y-FAPI-46 PET/CT. Predicted values on 68Ga-FAPI-46 PET/CT can help clinicians with diagnostic stratification and patient selection, with intratherapeutic verification remaining necessary before any individualization of administered activity.

单时间点[68Ga]Ga-FAPI-46 PET/CT成像预测肿瘤吸收剂量[90Y]
放射性标记成纤维细胞活化蛋白(FAP)靶向肽,如90Y-FAPI-46,已越来越多地用于治疗各种肿瘤实体,初步报告表明治疗反应具有可接受的毒性特征。剂量测定可以最大限度地提高抗肿瘤能力,减少副作用。本研究的目的是探讨90Y-FAPI-46肿瘤剂量学是否可以通过诊断性68Ga-FAPI-46 PET/CT数据预测。方法:14例患者共24个病灶,每隔3个月分别进行单时间点68Ga-FAPI-46 PET/CT扫描和3次90Y-FAPI-46 PET/CT扫描,进行剂量测定。在PET图像上识别肿瘤,并在低剂量CT上测量解剖肿瘤体积。采用90Y-FAPI-46数据计算注射时外推的肿瘤摄取、时间积分活度系数(TIAC)和肿瘤吸收剂量作为参考值,并通过单时间点剂量学模型与68Ga-FAPI-46数据的预测值进行比较。评估90Y-FAPI-46和68ga - fapi -46值之间的相关性。结果:使用单时间点68Ga-FAPI-46 PET/CT计算预测值时,90Y-FAPI-46在所有病变中的平均有效半衰期为8.44±1.73 h,肿瘤摄取、TIAC和肿瘤吸收剂量的平均±SD比(即使用68Ga-FAPI-46数据的预测值除以参考数据90Y-FAPI-46)分别为0.93±0.39、0.77±0.35和0.77±0.35。在Bland-Altman分析中,肿瘤摄取、TIAC和肿瘤吸收剂量的平均差异(偏差)±SD分别为-16.11%±43.28% (95% CI, -100.90 ~ 68.73%; Spearman ρ = 0.91; P < 0.0001)、-32.60%±41.26% (95% CI, -113.50 ~ 48.26%; Spearman ρ = 0.91; P < 0.0001)和-33.35%±40.19% (95% CI, -112.10 ~ 45.43%; Spearman ρ = 0.77; P < 0.0001)。结论:90Y-FAPI-46 PET/CT和68Ga-FAPI-46 PET/CT上的肿瘤摄取、TIAC和肿瘤吸收剂量高度相关,但68Ga-FAPI-46 PET/CT上的数值有低于90Y-FAPI-46 PET/CT的趋势。68Ga-FAPI-46 PET/CT的预测值可以帮助临床医生进行诊断分层和患者选择,在任何个体化给药活动之前,仍有必要进行治疗内验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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