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The value of [18F]FDG PET/CT in avoiding overtreatment of 131l avidity pulmonary metastasis of differentiated thyroid cancer
- Department of Nuclear Medicine, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
open access
Abstract
Introduction: We usually use 131I-whole body scan (131I-WBS) and serum thyroglobulin (Tg) values to determine whether differentiated thyroid cancer (DTC) patients need to receive 131I treatment, but not all 131I-avid (functioning) patients have a good response to 131I therapy. Our study aims to assess the data of [18F]fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography ([18F] FDG PET/CT) to research the status of 131I-avid pulmonary metastases (PMs) and the prognosis of the patients.
Material and methods: The 131I-avid PMs of DTC patients who underwent [18F]FDG PET/CT scans were included. The maximum standardized uptake value (SUVmax), metabolic tumour volume (MTV), and total lesion glycolysis (TLG) were used to estimate [18F]FDG uptake. The mean follow-up period was 34.14 ± 18.64 months. Progression-free survival (PFS) was estimated by the Kaplan-Meier method. The study was based on per-patient and per-lesion analyses.
Results: Among the 42 included patients, 34 (34/42, 81%) showed [18F]FDG uptake, which was defined as abnormal foci (SUVmax > 1.0) in the lungs. SUVmax, MTV, TLG, and tumour size were the factors that influenced the outcome of 131I treatment based on Tg levels (p = 0.000, 0.016, 0.000, 0.000) in per-lesion analysis. The only independent factor was the size of the lesion. There was a significant difference in response to 131I therapy between PMs with F-I+ and F+/I+ according to both Tg levels and Response Evaluation Criteria in Solid Tumours (RECIST) (version 1.1) (p = 0.044, 0.001), in the per-lesion analysis. When the changes in size or metabolism of some lesions are inconsistent the prognosis of these patients is poor (p = 0.003).
Conclusions: We concluded that higher [18F]FDG uptake and larger tumour size predict poor therapeutic effects and a high risk of disease progression in 131I-avid PMs of DTC. For evaluating the efficiency of 131I treatment, per-lesion analyses and assessing the data of [18F] FDG PET/CT would be more reliable than per-patient evaluation only. And early focal treatment modalities may improve their life span.
Abstract
Introduction: We usually use 131I-whole body scan (131I-WBS) and serum thyroglobulin (Tg) values to determine whether differentiated thyroid cancer (DTC) patients need to receive 131I treatment, but not all 131I-avid (functioning) patients have a good response to 131I therapy. Our study aims to assess the data of [18F]fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography ([18F] FDG PET/CT) to research the status of 131I-avid pulmonary metastases (PMs) and the prognosis of the patients.
Material and methods: The 131I-avid PMs of DTC patients who underwent [18F]FDG PET/CT scans were included. The maximum standardized uptake value (SUVmax), metabolic tumour volume (MTV), and total lesion glycolysis (TLG) were used to estimate [18F]FDG uptake. The mean follow-up period was 34.14 ± 18.64 months. Progression-free survival (PFS) was estimated by the Kaplan-Meier method. The study was based on per-patient and per-lesion analyses.
Results: Among the 42 included patients, 34 (34/42, 81%) showed [18F]FDG uptake, which was defined as abnormal foci (SUVmax > 1.0) in the lungs. SUVmax, MTV, TLG, and tumour size were the factors that influenced the outcome of 131I treatment based on Tg levels (p = 0.000, 0.016, 0.000, 0.000) in per-lesion analysis. The only independent factor was the size of the lesion. There was a significant difference in response to 131I therapy between PMs with F-I+ and F+/I+ according to both Tg levels and Response Evaluation Criteria in Solid Tumours (RECIST) (version 1.1) (p = 0.044, 0.001), in the per-lesion analysis. When the changes in size or metabolism of some lesions are inconsistent the prognosis of these patients is poor (p = 0.003).
Conclusions: We concluded that higher [18F]FDG uptake and larger tumour size predict poor therapeutic effects and a high risk of disease progression in 131I-avid PMs of DTC. For evaluating the efficiency of 131I treatment, per-lesion analyses and assessing the data of [18F] FDG PET/CT would be more reliable than per-patient evaluation only. And early focal treatment modalities may improve their life span.
Keywords
differentiated thyroid cancer; pulmonary metastasis; FDG avidity; radioiodine
Title
The value of [18F]FDG PET/CT in avoiding overtreatment of 131l avidity pulmonary metastasis of differentiated thyroid cancer
Journal
Issue
Article type
Original paper
Pages
385-391
Published online
2023-07-21
Page views
826
Article views/downloads
286
DOI
Pubmed
Bibliographic record
Endokrynol Pol 2023;74(4):385-391.
Keywords
differentiated thyroid cancer
pulmonary metastasis
FDG avidity
radioiodine
Authors
Zhongyun Xu
Chao Li
Fang Feng
Shuqi Wu
Hui Wang
Hongliang Fu
- Song HJ, Qiu ZL, Shen CT, et al. Pulmonary metastases in differentiated thyroid cancer: efficacy of radioiodine therapy and prognostic factors. Eur J Endocrinol. 2015; 173(3): 399–408.
- Liu M, Cheng L, Jin Y, et al. Predicting I-avidity of metastases from differentiated thyroid cancer using F-FDG PET/CT in postoperative patients with elevated thyroglobulin. Sci Rep. 2018; 8(1): 4352.
- Vansteenkiste JF, Stroobants SG, Dupont PJ, et al. Prognostic importance of the standardized uptake value on (18)F-fluoro-2-deoxy-glucose-positron emission tomography scan in non-small-cell lung cancer: An analysis of 125 cases. Leuven Lung Cancer Group. J Clin Oncol. 1999; 17(10): 3201–3206.
- Wang W. Prognostic Value of [18F]Fluorodeoxyglucose Positron Emission Tomographic Scanning in Patients with Thyroid Cancer. J Clin Endocrinol Metab. 2000; 85(3): 1107–1113.
- Vasko V, Hu S, Wu G, et al. High prevalence and possible de novo formation of BRAF mutation in metastasized papillary thyroid cancer in lymph nodes. J Clin Endocrinol Metab. 2005; 90(9): 5265–5269.
- Oler G, Ebina KN, Michaluart P, et al. Investigation of BRAF mutation in a series of papillary thyroid carcinoma and matched-lymph node metastasis reveals a new mutation in metastasis. Clin Endocrinol (Oxf). 2005; 62(4): 509–511.
- Abrosimov A, Saenko V, Rogounovitch T, et al. Different structural components of conventional papillary thyroid carcinoma display mostly identical BRAF status. Int J Cancer. 2007; 120(1): 196–200.
- Watanabe Ha, Okada M, Kaji Y, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Gan To Kagaku Ryoho. 2009; 36(13): 2495–501.
- Terroir M, Borget I, Bidault F, et al. The intensity of 18FDG uptake does not predict tumor growth in patients with metastatic differentiated thyroid cancer. Eur J Nucl Med Mol Imaging. 2017; 44(4): 638–646.
- Yoshio K, Sato S, Okumura Y, et al. The local efficacy of I-131 for F-18 FDG PET positive lesions in patients with recurrent or metastatic thyroid carcinomas. Clin Nucl Med. 2011; 36(2): 113–117.
- Kim M, Kim WGu, Park S, et al. Initial Size of Metastatic Lesions Is Best Prognostic Factor in Patients with Metastatic Differentiated Thyroid Carcinoma Confined to the Lung. Thyroid. 2017; 27(1): 49–58.
- Lim H, Devesa SS, Sosa JA, et al. Trends in Thyroid Cancer Incidence and Mortality in the United States, 1974-2013. JAMA. 2017; 317(13): 1338–1348.
- Moon SH, Cho SH, Park LC, et al. Metabolic response evaluated by 18F-FDG PET/CT as a potential screening tool in identifying a subgroup of patients with advanced non-small cell lung cancer for immediate maintenance therapy after first-line chemotherapy. Eur J Nucl Med Mol Imaging. 2013; 40(7): 1005–1013.
- Chao M. Management of differentiated thyroid cancer with rising thyroglobulin and negative diagnostic radioiodine whole body scan. Clin Oncol (R Coll Radiol). 2010; 22(6): 438–447.
- Stangierski A, Kaznowski J, Wolinski K, et al. The usefulness of fluorine-18 fluorodeoxyglucose PET in the detection of recurrence in patients with differentiated thyroid cancer with elevated thyroglobulin and negative radioiodine whole-body scan. Nucl Med Commun. 2016; 37(9): 935–938.
- Feine U, Lietzenmayer R, Hanke JP, et al. Fluorine-18-FDG and iodine-131-iodide uptake in thyroid cancer. J Nucl Med. 1996; 37(9): 1468–1472.
- Qiu ZL, Wei WJ, Shen CT, et al. Diagnostic Performance of F-FDG PET/CT in Papillary Thyroid Carcinoma with Negative I-WBS at first Postablation, Negative Tg and Progressively Increased TgAb Level. Sci Rep. 2017; 7(1): 2849.
- Wang R, Zhang Y, Tan J, et al. Analysis of radioiodine therapy and prognostic factors of differentiated thyroid cancer patients with pulmonary metastasis: An 8-year retrospective study. Medicine (Baltimore). 2017; 96(19): e6809.
- Grünwald F, K�licke T, Feine U, et al. Fluorine-18 fluorodeoxyglucose positron emission tomography in thyroid cancer: results of a multicentre study. Eur J Nucl Med. 1999; 26(12): 1547–1552.
- Shiga T, Tsukamoto E, Nakada K, et al. Comparison of (18) F-FDG, (131) I-Na, and (201) Tl in diagnosis of recurrent or metastatic thyroid carcinoma. J Nucl Med. 2001; 42(3): 414–419.
- Netea-Maier RT, Klück V, Plantinga TS, et al. Autophagy in thyroid cancer: present knowledge and future perspectives. Front Endocrinol (Lausanne). 2015; 6: 22.
- Min JJ, Chung JK, Lee Y, et al. Relationship between expression of the sodium/iodide symporter and (131)I uptake in recurrent lesions of differentiated thyroid carcinoma. Eur J Nucl Med. 2001; 28(5): 639–645.
- Sohn SY, Kim HIn, Kim YN, et al. Prognostic indicators of outcomes in patients with lung metastases from differentiated thyroid carcinoma during long-term follow-up. Clin Endocrinol (Oxf). 2018; 88(2): 318–326.