Increased lesion detectability in patients with locally advanced breast cancer-A pilot study using dynamic whole-body [18F]FDG PET/CT.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Mette Abildgaard Pedersen, André H Dias, Karin Hjorthaug, Lars C Gormsen, Joan Fledelius, Anna Lyhne Johnsson, Signe Borgquist, Trine Tramm, Ole Lajord Munk, Mikkel Holm Vendelbo
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引用次数: 0

Abstract

Background: Accurate diagnosis of axillary lymph node (ALN) metastases is essential for prognosis and treatment planning in breast cancer. Evaluation of ALN is done by ultrasound, which is limited by inter-operator variability, and by sentinel lymph node biopsy and/or ALN dissection, none of which are without risks and/or long-term complications. It is known that conventional 2-deoxy-2-[18F]fluoro-D-glucose ([18F]FDG) positron emission tomography/computed tomography (PET/CT) has limited sensitivity for ALN metastases. However, a recently developed dynamic whole-body (D-WB) [18F]FDG PET/CT scanning protocol, allowing for imaging of tissue [18F]FDG metabolic rate (MRFDG), has been shown to have the potential to increase lesion detectability. The study purpose was to examine detectability of malignant lesions in D-WB [18F]FDG PET/CT compared to conventional [18F]FDG PET/CT.

Results: This study prospectively included ten women with locally advanced breast cancer who were referred for an [18F]FDG PET/CT as part of their diagnostic work-up. They all underwent D-WB [18F]FDG PET/CT, consisting of a 6 min single bed dynamic scan over the chest region started at the time of tracer injection, a 64 min dynamic WB PET scan consisting of 16 continuous bed motion passes, and finally a contrast-enhanced CT scan, with generation of MRFDG parametric images. Lesion visibility was assessed by tumor-to-background and contrast-to-noise ratios using volumes of interest isocontouring tumors with a set limit of 50% of SUVmax and background volumes placed in the vicinity of tumors. Lesion visibility was best in the MRFDG images, with target-to-background values 2.28 (95% CI: 2.04-2.54) times higher than target-to-background values in SUV images, and contrast-to-noise values 1.23 (95% CI: 1.12-1.35) times higher than contrast-to-noise values in SUV images. Furthermore, five imaging experts visually assessed the images and three additional suspicious lesions were found in the MRFDG images compared to SUV images; one suspicious ALN, one suspicious parasternal lymph node, and one suspicious lesion located in the pelvic bone.

Conclusions: D-WB [18F]FDG PET/CT with MRFDG images show potential for improved lesion detectability compared to conventional SUV images in locally advanced breast cancer. Further validation in larger cohorts is needed.

Clinical trial registration: The trial is registered in clinicaltrials.gov, NCT05110443, https://www.

Clinicaltrials: gov/study/NCT05110443?term=NCT05110443&rank=1 .

提高局部晚期乳腺癌患者病灶的可探测性--一项使用动态全身[18F]FDG PET/CT 的试点研究。
背景:准确诊断腋窝淋巴结(ALN)转移对乳腺癌的预后和治疗计划至关重要。对腋窝淋巴结的评估主要通过超声波和前哨淋巴结活检及/或腋窝淋巴结清扫来进行,但超声波和前哨淋巴结活检受限于操作者之间的差异,而前哨淋巴结活检和/或腋窝淋巴结清扫均无风险和/或长期并发症。众所周知,传统的 2-脱氧-2-[18F]氟-D-葡萄糖([18F]FDG)正电子发射断层扫描/计算机断层扫描(PET/CT)对 ALN 转移的敏感性有限。然而,最近开发的动态全身(D-WB)[18F]FDG PET/CT 扫描方案允许对组织[18F]FDG 代谢率(MRFDG)进行成像,已被证明有可能提高病灶的可探测性。研究目的是检验 D-WB [18F]FDG PET/CT 与传统 [18F]FDG PET/CT 相比对恶性病变的可探测性:本研究前瞻性地纳入了十名患有局部晚期乳腺癌的女性患者,她们在诊断过程中都接受了[18F]FDG PET/CT检查。她们都接受了D-WB[18F]FDG PET/CT检查,包括注射示踪剂时开始的胸部区域6分钟单床动态扫描、由16个连续床移动通道组成的64分钟动态WB PET扫描,以及最后的对比增强CT扫描,并生成MRFDG参数图像。病变可见度是通过肿瘤与背景和对比度与噪声的比率来评估的,使用的感兴趣体积与肿瘤等高,SUVmax 设定为 50%,背景体积放置在肿瘤附近。MRFDG图像中的病变可见度最高,目标-背景值是SUV图像中目标-背景值的2.28倍(95% CI:2.04-2.54),对比度-噪声值是SUV图像中对比度-噪声值的1.23倍(95% CI:1.12-1.35)。此外,五位影像学专家对图像进行了目测评估,与 SUV 图像相比,MRFDG 图像中发现了三个额外的可疑病灶:一个可疑 ALN、一个可疑胸骨旁淋巴结和一个位于盆骨的可疑病灶:结论:与传统的 SUV 图像相比,D-WB [18F]FDG PET/CT 与 MRFDG 图像显示出在局部晚期乳腺癌中提高病灶可探测性的潜力。需要在更大的队列中进一步验证:该试验已在 clinicaltrials.gov 注册,编号为 NCT05110443,https://www.Clinicaltrials: gov/study/NCT05110443?term=NCT05110443&rank=1 。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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