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评估18F-FDG大视野PET在肿瘤分期中的潜在应用价值:病变数量及摄取情况评估

Assessing the Potential Usefulness of FDG LAFOV-PET for Oncological Staging: An Evaluation of Lesion Number and Uptake.

作者信息

Dragonetti Valentino, Peluso Sara, Castellani Gastone, Fanti Stefano

机构信息

Nuclear Medicine, Alma Mater Studiorum-University of Bologna, 40126 Bologna, Italy.

Department of Medical and Surgical Sciences, Alma Mater Studiorum-University of Bologna, 40126 Bologna, Italy.

出版信息

Cancers (Basel). 2025 Jun 10;17(12):1927. doi: 10.3390/cancers17121927.

DOI:10.3390/cancers17121927
PMID:40563577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12191386/
Abstract

: In many cases, the detection of a single lesion could revolutionise patient clinical management; not all localisations, especially those with a low uptake and, consequently, a low Tumour-to-Background Ratio (TBR), are readily detectable using [F]F-FDG PET/CT. LAFOV-PET offers a potential enhancement in lesion detection, but the proportion of patients who would benefit from its use has yet to be determined. With the present analysis, we aimed to assess which clinical contexts the enhancement in lesion detection could affect the most. : This retrospective study included 764 patients who underwent [F]F-FDG PET/CT between January and April 2024. Data were obtained through a review of PET/CT reports. Inclusion criteria comprised patients who attended our centre for cancer pathologies or masses of undetermined nature (MUNs) in a staging setting, excluding patients who had undergone a prior [F]F-FDG PET/CT scan or who had received therapy for any cancer pathology. This analysis focused on the total number of lesions identified, as well as the SUVmax of the lesion with the highest uptake. We analysed the proportion of patients who were within the range of number of lesions between 1 and 2, as well as who had an SUVmax of the lesion with the highest uptake between 2 and 5, either in the whole patient population or in the pathologies with a larger numerosity in the present study. : Among the 862 scans analysed, 289 (34%) were found to be negative, while 573 (66%) presented at least one localisation. In total, 4.5% of patients presented both a lesion number of between 1 and 2 and an SUVmax of the lesion with the highest uptake between 2 and 5. Among the malignancies that were the most common in the analysed population, a higher-than-average proportion of patients meeting these criteria were found in melanoma (6.2%), breast cancer (5.9%), and multiple myeloma (4.8%) patients. Conversely, the conditions that presented a lower proportion of patients in this range were suffering from MUNs (4.0%), lung cancer (2.1%), head-neck cancer (2.1%), suspected lymphoma (2.0%), and colon cancer (0.0%). : Our analysis shows that almost 1 in 20 patients evaluated at oncological staging with [F]F-FDG PET/CT could benefit from the increased diagnostic sensitivity offered by LAFOV-PET scanners. These data, although preliminary, support the need for future prospective controlled studies to confirm the actual clinical impact of implementing LAFOV-PET in current practice.

摘要

在许多情况下,检测到单个病灶可能会彻底改变患者的临床管理;并非所有定位,尤其是那些摄取量低、因此肿瘤与本底比值(TBR)低的病灶,使用[F]F-FDG PET/CT都能轻易检测到。大视野PET有望提高病灶检测能力,但受益于其使用的患者比例尚未确定。通过本分析,我们旨在评估病灶检测能力的提高在哪些临床情况下影响最大。

这项回顾性研究纳入了2024年1月至4月期间接受[F]F-FDG PET/CT检查的764例患者。数据通过查阅PET/CT报告获得。纳入标准包括在分期检查中因癌症病理或性质未明的肿块(MUNs)到我们中心就诊的患者,排除之前接受过[F]F-FDG PET/CT扫描或接受过任何癌症病理治疗的患者。本分析重点关注识别出的病灶总数,以及摄取量最高的病灶的最大标准化摄取值(SUVmax)。我们分析了病灶数量在1至2个范围内,以及摄取量最高的病灶的SUVmax在2至5之间的患者比例,无论是在整个患者群体中,还是在本研究中数量较多的病理类型中。

在分析的862次扫描中,289次(34%)结果为阴性,而573次(66%)至少有一个定位。总体而言,4.5%的患者病灶数量在1至2个之间,且摄取量最高的病灶的SUVmax在2至5之间。在分析人群中最常见的恶性肿瘤中,黑色素瘤(6.2%)、乳腺癌(5.9%)和多发性骨髓瘤(4.8%)患者中符合这些标准的患者比例高于平均水平。相反,在此范围内患者比例较低的疾病包括MUNs(4.0%)、肺癌(2.1%)、头颈癌(2.1%)、疑似淋巴瘤(2.0%)和结肠癌(0.0%)。

我们的分析表明,在肿瘤分期时接受[F]F-FDG PET/CT检查的患者中,几乎每20人中有1人可能受益于大视野PET扫描仪提供的更高诊断敏感性。这些数据虽然是初步的,但支持未来进行前瞻性对照研究,以确认在当前实践中应用大视野PET的实际临床影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/33c6548693c7/cancers-17-01927-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/5ef4329da294/cancers-17-01927-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/ed56bd11674c/cancers-17-01927-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/f7b641a8e92b/cancers-17-01927-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/33c6548693c7/cancers-17-01927-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/5ef4329da294/cancers-17-01927-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/ed56bd11674c/cancers-17-01927-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/f7b641a8e92b/cancers-17-01927-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69a4/12191386/33c6548693c7/cancers-17-01927-g004.jpg

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本文引用的文献

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