[<sup>18</sup>F]AlF-NOTA-FAPI-04 PET/CT for Predicting Pathologic Response of Resectable Esophageal Squamous Cell Carcinoma to Neoadjuvant Camrelizumab and Chemotherapy: A Phase II Clinical Trial

This single-center, single-arm, phase II trial (ChiCTR2100050057) investigated the ability of <sup>18</sup>F-labeled fibroblast activation protein inhibitor ([<sup>18</sup>F]AlF-NOTA-FAPI-04, denoted as <sup>18</sup>F-FAPI) PET/CT to predict the response to neoadjuvant camrelizumab plus chemotherapy (nCC) in locally advanced esophageal squamous cell carcinoma (LA-ESCC). <b>Methods:</b> This study included 32 newly diagnosed LA-ESCC participants who underwent <sup>18</sup>F-FAPI PET/CT at baseline, of whom 23 also underwent scanning after 2 cycles of nCC. The participants underwent surgery after 2 cycles of nCC. Recorded PET parameters included maximum, peak, and mean SUVs and tumor-to-background ratios (TBRs), metabolic tumor volume, and total lesion FAP expression. PET parameters were compared between patient groups with good and poor pathologic responses, and the predictive performance for treatment response was analyzed. <b>Results:</b> The good and poor response groups each included 16 participants (16/32, 50.0%). On <sup>18</sup>F-FAPI PET/CT, the posttreatment SUVs were significantly lower in good responders than in poor responders, whereas the changes in SUVs with treatment were significantly higher (all <i>P</i> < 0.05). SUV<sub>max</sub> (area under the curve [AUC], 0.87; <i>P</i> = 0.0026), SUV<sub>peak</sub> (AUC, 0.89; <i>P</i> = 0.0017), SUV<sub>mean</sub> (AUC, 0.88; <i>P</i> = 0.0021), TBR<sub>max</sub> (AUC, 0.86; <i>P</i> = 0.0031), and TBR<sub>mean</sub> (AUC, 0.88; <i>P</i> = 0.0021) after nCC were significant predictors of pathologic response to nCC, with sensitivities of 63.64%-81.82% and specificities of 83.33%-100%. Changes in SUV<sub>max</sub> (AUC, 0.81; <i>P</i> = 0.0116), SUV<sub>peak</sub> (AUC, 0.82; <i>P</i> = 0.0097), SUV<sub>mean</sub> (AUC, 0.81; <i>P</i> = 0.0116), and TBR<sub>mean</sub> (AUC, 0.74; <i>P</i> = 0.0489) also were significant predictors of the pathologic response to nCC, with sensitivities and specificities in similar ranges. <b>Conclusion:</b> <sup>18</sup>F-FAPI PET/CT parameters after treatment and their changes from baseline can predict the pathologic response to nCC in LA-ESCC participants.

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Publication Details

Journal
Journal of Nuclear Medicine
Published
2024-09-26
DOI
https://doi.org/10.2967/jnumed.124.268557
Citations
9
Primary Topic
Esophageal Cancer Research and Treatment
Type
article
Field-Weighted Citation Impact
5.15

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article

[18F]AlF-NOTA-FAPI-04 PET/CT for Predicting Pathologic Response of Resectable Esophageal Squamous Cell Carcinoma to Neoadjuvant Camrelizumab and Chemotherapy: A Phase II Clinical Trial

Xinying Hu, Zhendan Wang, Shuanghu Yuan, Shuguang Liu et al.
9 citations
Journal of Nuclear Medicine
Esophageal Cancer Research and Treatment
5.15
article

[18F]AlF-NOTA-FAPI-04 PET/CT for Predicting Pathologic Response of Resectable Esophageal Squamous Cell Carcinoma to Neoadjuvant Camrelizumab and Chemotherapy: A Phase II Clinical Trial

Xinying Hu, Zhendan Wang, Shuanghu Yuan, Shuguang Liu, Yuchun Wei, Yuhong Sun, Jinming Yu, Qiming Qin, Yinjun Dong, Jingjie Qin
article en
9 citations

Abstract

This single-center, single-arm, phase II trial (ChiCTR2100050057) investigated the ability of <sup>18</sup>F-labeled fibroblast activation protein inhibitor ([<sup>18</sup>F]AlF-NOTA-FAPI-04, denoted as <sup>18</sup>F-FAPI) PET/CT to predict the response to neoadjuvant camrelizumab plus chemotherapy (nCC) in locally advanced esophageal squamous cell carcinoma (LA-ESCC). <b>Methods:</b> This study included 32 newly diagnosed LA-ESCC participants who underwent <sup>18</sup>F-FAPI PET/CT at baseline, of whom 23 also underwent scanning after 2 cycles of nCC. The participants underwent surgery after 2 cycles of nCC. Recorded PET parameters included maximum, peak, and mean SUVs and tumor-to-background ratios (TBRs), metabolic tumor volume, and total lesion FAP expression. PET parameters were compared between patient groups with good and poor pathologic responses, and the predictive performance for treatment response was analyzed. <b>Results:</b> The good and poor response groups each included 16 participants (16/32, 50.0%). On <sup>18</sup>F-FAPI PET/CT, the posttreatment SUVs were significantly lower in good responders than in poor responders, whereas the changes in SUVs with treatment were significantly higher (all <i>P</i> < 0.05). SUV<sub>max</sub> (area under the curve [AUC], 0.87; <i>P</i> = 0.0026), SUV<sub>peak</sub> (AUC, 0.89; <i>P</i> = 0.0017), SUV<sub>mean</sub> (AUC, 0.88; <i>P</i> = 0.0021), TBR<sub>max</sub> (AUC, 0.86; <i>P</i> = 0.0031), and TBR<sub>mean</sub> (AUC, 0.88; <i>P</i> = 0.0021) after nCC were significant predictors of pathologic response to nCC, with sensitivities of 63.64%-81.82% and specificities of 83.33%-100%. Changes in SUV<sub>max</sub> (AUC, 0.81; <i>P</i> = 0.0116), SUV<sub>peak</sub> (AUC, 0.82; <i>P</i> = 0.0097), SUV<sub>mean</sub> (AUC, 0.81; <i>P</i> = 0.0116), and TBR<sub>mean</sub> (AUC, 0.74; <i>P</i> = 0.0489) also were significant predictors of the pathologic response to nCC, with sensitivities and specificities in similar ranges. <b>Conclusion:</b> <sup>18</sup>F-FAPI PET/CT parameters after treatment and their changes from baseline can predict the pathologic response to nCC in LA-ESCC participants.

Journal of Nuclear MedicineVol. 65(11)
University of Science and Technology of China (CN), Shandong Tumor Hospital (CN), Shandong First Medical University (CN)
Jiangsu Hengrui Medicine
Zero hunger
Openalex Percentile: Top 4%
Esophageal Cancer Research and Treatment
5.15
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