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      [ 18F]FAPI-42 PET/CT in differentiated thyroid cancer: diagnostic performance, uptake values, and comparison with 2-[ 18F]FDG PET/CT

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          Abstract

          Purpose

          This study aimed to assess the diagnostic performance of [ 18F]FAPI-42 PET/CT and compare it with that of 2-[ 18F]FDG PET/CT in patients with differentiated thyroid cancer (DTC) with biochemical elevations in Tg or anti-Tg antibodies.

          Methods

          A total of 42 patients with DTC with biochemical elevations in Tg or anti-Tg antibodies underwent [ 18F]FAPI-42 PET/CT as part of this study; of which, 11 additionally underwent 2-[ 18F]FDG PET/CT within 7 days. Images were semi-quantitatively and visually interpreted, and the quantity, location, and uptake values of lesions were noted. The diagnostic capacity of [ 18F]FAPI-42 PET/CT and biomarkers affecting the uptake of [ 18F]FAPI-42 were evaluated. In addition, the diagnostic performance and uptake of [ 18F]FAPI-42 and 2-[ 18F]FDG were compared, and the correlation between lesion diameter and quantitative parameters was investigated.

          Results

          A total of 161 lesions were detected in 27 (64%) patients on [ 18F]FAPI-42 PET/CT. FAPI-positive local recurrence showed the highest uptake intensity, followed by lymphatic, other site-associated (bone and pleura), and pulmonary lesions (mean SUV max, 4.7 versus 3.7 versus 3.0 versus 2.2, respectively; P < 0.0001). The levels of TSH, Tg, and Tg-Ab did not affect the uptake value of lesions (median SUV max: 2.4 versus 3.2, P = 0.56; 2.9 versus 2.4, P = 0.0935; 2.8 versus 2.6, P = 0.0525, respectively). A total of 90 positive lesions were detected in 7 patients using both modalities. All positive lesions showed statistically higher uptake of 2-[ 18F]FDG than that of [ 18F]FAPI-42 (SUV max, 2.6 versus 2.1; P = 0.026). However, the SUV max of [ 18F]FAPI-42 was higher than that of 2-[ 18F]FDG in local recurrences and lymphatic lesions (SUV max, 4.2 versus 2.9 and 3.9 versus 3.4, respectively; P > 0.05).

          Conclusion

          [ 18F]FAPI-42 can be used for detecting lesions and reflecting FAP expression during local recurrence and metastasis in patients with DTC with biochemical elevations in Tg or anti-Tg antibodies. The diagnostic performance of [ 18F]FAPI-42 PET/CT is comparable with that of 2-[ 18F]FDG PET/CT in such patients.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s00259-022-06067-2.

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          Most cited references31

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          Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries

          This article provides an update on the global cancer burden using the GLOBOCAN 2020 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer. Worldwide, an estimated 19.3 million new cancer cases (18.1 million excluding nonmelanoma skin cancer) and almost 10.0 million cancer deaths (9.9 million excluding nonmelanoma skin cancer) occurred in 2020. Female breast cancer has surpassed lung cancer as the most commonly diagnosed cancer, with an estimated 2.3 million new cases (11.7%), followed by lung (11.4%), colorectal (10.0 %), prostate (7.3%), and stomach (5.6%) cancers. Lung cancer remained the leading cause of cancer death, with an estimated 1.8 million deaths (18%), followed by colorectal (9.4%), liver (8.3%), stomach (7.7%), and female breast (6.9%) cancers. Overall incidence was from 2-fold to 3-fold higher in transitioned versus transitioning countries for both sexes, whereas mortality varied <2-fold for men and little for women. Death rates for female breast and cervical cancers, however, were considerably higher in transitioning versus transitioned countries (15.0 vs 12.8 per 100,000 and 12.4 vs 5.2 per 100,000, respectively). The global cancer burden is expected to be 28.4 million cases in 2040, a 47% rise from 2020, with a larger increase in transitioning (64% to 95%) versus transitioned (32% to 56%) countries due to demographic changes, although this may be further exacerbated by increasing risk factors associated with globalization and a growing economy. Efforts to build a sustainable infrastructure for the dissemination of cancer prevention measures and provision of cancer care in transitioning countries is critical for global cancer control.
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              FDG PET/CT: EANM procedure guidelines for tumour imaging: version 2.0

              The purpose of these guidelines is to assist physicians in recommending, performing, interpreting and reporting the results of FDG PET/CT for oncological imaging of adult patients. PET is a quantitative imaging technique and therefore requires a common quality control (QC)/quality assurance (QA) procedure to maintain the accuracy and precision of quantitation. Repeatability and reproducibility are two essential requirements for any quantitative measurement and/or imaging biomarker. Repeatability relates to the uncertainty in obtaining the same result in the same patient when he or she is examined more than once on the same system. However, imaging biomarkers should also have adequate reproducibility, i.e. the ability to yield the same result in the same patient when that patient is examined on different systems and at different imaging sites. Adequate repeatability and reproducibility are essential for the clinical management of patients and the use of FDG PET/CT within multicentre trials. A common standardised imaging procedure will help promote the appropriate use of FDG PET/CT imaging and increase the value of publications and, therefore, their contribution to evidence-based medicine. Moreover, consistency in numerical values between platforms and institutes that acquire the data will potentially enhance the role of semiquantitative and quantitative image interpretation. Precision and accuracy are additionally important as FDG PET/CT is used to evaluate tumour response as well as for diagnosis, prognosis and staging. Therefore both the previous and these new guidelines specifically aim to achieve standardised uptake value harmonisation in multicentre settings.
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                Author and article information

                Contributors
                fuwei19700513@163.com
                maojingsong163@163.com
                Journal
                Eur J Nucl Med Mol Imaging
                Eur J Nucl Med Mol Imaging
                European Journal of Nuclear Medicine and Molecular Imaging
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                1619-7070
                1619-7089
                10 December 2022
                10 December 2022
                2023
                : 50
                : 4
                : 1205-1215
                Affiliations
                [1 ]GRID grid.443385.d, ISNI 0000 0004 1798 9548, Department of Nuclear Medicine, Affiliated Hospital, , Guilin Medical University, ; Guilin, China
                [2 ]GRID grid.443385.d, ISNI 0000 0004 1798 9548, Department of Vascular Intervention, Affiliated Hospital, , Guilin Medical University, ; Guilin, China
                [3 ]Xiamen Key Laboratory of Endocrine-Related Cancer Precision Medicine, Xiamen, 361101 China
                Article
                6067
                10.1007/s00259-022-06067-2
                9931817
                36495325
                5c8b42a8-6dff-4405-98f5-9ac5f33b01de
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 9 September 2022
                : 28 November 2022
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2023

                Radiology & Imaging
                [18f]fapi-42,2-[18f]fdg,differentiated thyroid cancer,pet/ct
                Radiology & Imaging
                [18f]fapi-42, 2-[18f]fdg, differentiated thyroid cancer, pet/ct

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