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[F]四氟硼酸盐PET-CT相较于[I]碘闪烁扫描术对复发性分化型甲状腺癌的增量诊断价值。

Incremental diagnostic value of [F]tetrafluoroborate PET-CT compared to [I]iodine scintigraphy in recurrent differentiated thyroid cancer.

作者信息

Dittmann Matthias, Gonzalez Carvalho José Manuel, Rahbar Kambiz, Schäfers Michael, Claesener Michael, Riemann Burkhard, Seifert Robert

机构信息

Department of Nuclear Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, 48149, Münster, Germany.

European Institute for Molecular Imaging (EIMI), University of Münster, Münster, Germany.

出版信息

Eur J Nucl Med Mol Imaging. 2020 Oct;47(11):2639-2646. doi: 10.1007/s00259-020-04727-9. Epub 2020 Apr 4.

DOI:10.1007/s00259-020-04727-9
PMID:32248325
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7515952/
Abstract

INTRODUCTION

Efficient therapy of recurrent differentiated thyroid cancer (DTC) is dependent on precise molecular imaging techniques targeting the human sodium iodide symporter (hNIS), which is a marker both of thyroid and DTC cells. Various iodine isotopes have been utilized for detecting DTC; however, these come with unfavorable radiation exposure and image quality ([I]iodine) or limited availability ([I]iodine). In contrast, [F]tetrafluoroborate (TFB) is a novel radiolabeled PET substrate of hNIS, results in PET images with high-quality and low radiation doses, and should therefore be suited for imaging of DTC. The aim of the present study was to compare the diagnostic performance of [F]TFB-PET to the clinical reference standard [I]iodine scintigraphy in patients with recurrent DTC.

METHODS

Twenty-five patients with recurrent DTC were included in this retrospective analysis. All patients underwent [F]TFB-PET combined with either CT or MRI due to newly discovered elevated TG levels, antiTG levels, sonographically suspicious cervical lymph nodes, or combinations of these findings. Correlative [I]iodine whole-body scintigraphy (dxWBS) including SPECT-CT was present for all patients; correlative [F]FDG-PET-CT was present for 21 patients. Histological verification of [F]TFB positive findings was available in 4 patients.

RESULTS

[F]TFB-PET detected local recurrence or metastases of DTC in significantly more patients than conventional [I]iodine dxWBS and SPECT-CT (13/25 = 52% vs. 3/25 = 12%, p = 0.002). The diagnosis of 6 patients with cervical lymph node metastases that showed mildly increased FDG metabolism but negative [I]iodine scintigraphy was changed: [F]TFB-PET revealed hNIS expression in the metastases, which were therefore reclassified as only partly de-differentiated (histological confirmation present in two patients). Highest sensitivity for detecting recurrent DTC had the combination of [F]TFB-PET-CT/MRI with [F]FDG-PET-CT (64%).

CONCLUSION

In the present cohort, [F]TFB-PET shows higher sensitivity and accuracy than [I]iodine WBS and SPECT-CT in detecting recurrent DTC. The combination of [F]TFB-PET with [F]FDG-PET-CT seems a reasonable strategy to characterize DTC tumor manifestations with respect to their differentiation and thereby also individually plan and monitor treatment. Future prospective studies evaluating the potential of [F]TFB-PET in recurrent DTC are warranted.

摘要

引言

复发性分化型甲状腺癌(DTC)的有效治疗依赖于针对人钠碘同向转运体(hNIS)的精确分子成像技术,hNIS是甲状腺和DTC细胞的标志物。各种碘同位素已被用于检测DTC;然而,这些方法存在辐射暴露和图像质量不佳([I]碘)或可用性有限([I]碘)的问题。相比之下,[F]四氟硼酸盐(TFB)是一种新型的hNIS放射性标记PET底物,可产生高质量和低辐射剂量的PET图像,因此应适用于DTC的成像。本研究的目的是比较[F]TFB-PET与临床参考标准[I]碘闪烁扫描在复发性DTC患者中的诊断性能。

方法

本回顾性分析纳入了25例复发性DTC患者。由于新发现的甲状腺球蛋白(TG)水平升高、抗TG水平升高、超声检查可疑的颈部淋巴结或这些发现的组合,所有患者均接受了[F]TFB-PET联合CT或MRI检查。所有患者均进行了包括SPECT-CT的相关[I]碘全身闪烁扫描(dxWBS);21例患者进行了相关的[F]FDG-PET-CT检查。4例患者可获得[F]TFB阳性结果的组织学验证。

结果

[F]TFB-PET检测到DTC局部复发或转移的患者明显多于传统的[I]碘dxWBS和SPECT-CT(13/25 = 52% vs. 3/25 = 12%,p = 0.002)。6例颈部淋巴结转移患者的诊断发生了改变,这些患者的FDG代谢轻度增加但[I]碘闪烁扫描为阴性:[F]TFB-PET显示转移灶中有hNIS表达,因此这些转移灶被重新分类为仅部分去分化(2例患者有组织学证实)。[F]TFB-PET-CT/MRI与[F]FDG-PET-CT联合检测复发性DTC的敏感性最高(64%)。

结论

在本队列中,[F]TFB-PET在检测复发性DTC方面显示出比[I]碘WBS和SPECT-CT更高的敏感性和准确性。[F]TFB-PET与[F]FDG-PET-CT联合似乎是一种合理的策略,可根据DTC肿瘤表现的分化情况进行特征化,从而也能单独规划和监测治疗。有必要进行未来的前瞻性研究,评估[F]TFB-PET在复发性DTC中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/d31861f1ff74/259_2020_4727_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/672f659e87f5/259_2020_4727_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/91924aff0d90/259_2020_4727_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/b21ad57fb468/259_2020_4727_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/d31861f1ff74/259_2020_4727_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/672f659e87f5/259_2020_4727_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/9c7b8c3e0ea6/259_2020_4727_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/91924aff0d90/259_2020_4727_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/b21ad57fb468/259_2020_4727_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/7515952/d31861f1ff74/259_2020_4727_Fig5_HTML.jpg

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