18F-FAPI-42 PET/CT和18F-FDG PET/CT在恶性消化系统肿瘤患者中的对比研究

IF 3 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Molecular Imaging and Biology Pub Date : 2025-02-01 Epub Date: 2025-01-13 DOI:10.1007/s11307-025-01982-w
Min Xiong, HongJi You, Jingmin Feng, Yipei Liu, Xiaoming Luo, Ying Liu, Sheng-Nan Jiang
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引用次数: 0

摘要

目的:放射性核素标记成纤维细胞活化蛋白抑制剂(FAPI)是一种新兴的肿瘤示踪剂。我们试图评估18F- fapi -42 PET/CT与同时使用2-脱氧-2[18F]氟-d -葡萄糖(18F- fdg) PET/CT在恶性消化系统肿瘤患者原发性和转移性病变中的摄取和诊断性能,并确定其潜在的临床益处。方法:纳入42例同时行18F-FDG PET/CT和18F-FAPI-42 PET/CT诊断、分期和再分期的患者(男30例,女12例,平均年龄56.71±13.26岁)。定量数据包括标准化摄取值(SUV)、肿瘤与肝脏比值(TLR)和肿瘤与血液池比值(TBR)进行分析。两名独立的阅读者对PET/CT图像上的病变数量和位置进行了视觉评估。使用Cohen’s kappa (κ)计算两次检查之间的观察者间一致性。结果:原发肿瘤部位包括肝脏(n = 20)、胃(n = 9)、胰腺(n = 5)和肠道(n = 10)。与18F-FDG相比,在大多数原发性和转移性病变中检测到更强的18F-FAPI-42摄取和更高的肿瘤-背景对比度,有助于提高诊断准确率,范围从95.24%到100%。此外,在原发性、局部和远处转移性病变中,特别是在多发性肝脏和腹膜转移性病变中,还可见18F-FAPI-42摄取。基于患者的观察者间一致性从中等到强烈不等,原发肿瘤观察到次优结果(κ = 0.441, P = 0.01),转移性肝脏和骨病变观察到较好的结果(κ = 1和0.896),p18f - fapi -42 PET/CT导致40.48%(17/42)患者改变治疗策略,而18F-FDG PET/CT仅导致4.8%(2/42)患者改变治疗方案。结论:在特定的消化系统恶性肿瘤患者中,我们的研究表明,与18F-FDG相比,18F-FAPI-42 PET/CT具有更高的吸收率和更好的病变可视化,是评估原发肿瘤和转移以及辅助分期、再分期和决策的有希望的替代方法。此外,它可能有助于fap靶向治疗或免疫治疗的治疗选择和疗效评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
18F-FAPI-42 PET/CT and 18F-FDG PET/CT in Patients with Malignant Digestive System Neoplasms: A Head-to-Head Comparative Study.

Purpose: Radionuclide-labeled fibroblast activation protein inhibitor (FAPI) is an emerging tumor tracer. We sought to assess the uptake and diagnostic performance of 18F-FAPI-42 PET/CT compared with simultaneous 2-deoxy-2[18F]fluoro-D-glucose (18F-FDG) PET/CT in primary and metastatic lesions in patients with malignant digestive system neoplasms and to determine the potential clinical benefit.

Procedures: Forty-two patients (men = 30, women = 12, mean age = 56.71 ± 13.26 years) who underwent 18F-FDG PET/CT and 18F-FAPI-42 PET/CT simultaneously for diagnosis, staging, and restaging were enrolled. Quantitative data, including standardized uptake value (SUV), tumor-to-liver ratio (TLR), and tumor-to-blood pool ratio (TBR), were analyzed. Two independent readers performed a visual assessment of lesion number and location on PET/CT images. Interobserver agreement between two examinations was calculated using Cohen's kappa (κ).

Results: Primary tumor locations included the liver (n = 20), stomach (n = 9), pancreas (n = 5), and intestine (n = 10). More intense 18F-FAPI-42 uptake and higher tumor-to-background contrast were detected in most primary and metastatic lesions compared with 18F-FDG, contributing to improved diagnostic accuracy ranging from 95.24% to 100%. Moreover, additional lesions showing 18F-FAPI-42 uptake in primary, locoregional and distant metastatic lesions were visualized, especially in multiple liver and peritoneal metastases. Patient-based interobserver agreement varied from moderate to strong, with suboptimal outcomes observed in primary tumors (κ = 0.441, P = 0.01) and preferable results derived from metastatic liver and bone lesions (κ = 1 and 0.896, both P < 0.01). 18F-FAPI-42 PET/CT resulted in modified treatment strategies for 40.48% (17/42) of patients, while 18F-FDG PET/CT led to altered therapeutic regimens in only 4.8% (2/42) of patients.

Conclusions: In selected patients with malignant digestive system neoplasms, our study shows that 18F-FAPI-42 PET/CT is a promising alternative for assessing primary tumors and metastases and aiding staging, restaging, and decision-making, with higher uptake and better lesion visualization compared with 18F-FDG. Additionally, it may shed light into the treatment selection and response assessment for FAP-targeted therapy or immunotherapy.

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来源期刊
CiteScore
6.90
自引率
3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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