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68Ga-PSMA PET/CT in radioactive iodine-refractory differentiated thyroid cancer and first treatment results with 177Lu-PSMA-617
被引:73
作者:
de Vries, Lisa H.
[1
]
Lodewijk, Lutske
[1
]
Braat, Arthur J. A. T.
[2
]
Krijger, Gerard C.
[2
]
Valk, Gerlof D.
[3
]
Lam, Marnix G. E. H.
[2
]
Rinkes, Inne H. M.
[1
]
Vriens, Menno R.
[1
]
de Keizer, Bart
[2
]
机构:
[1] Univ Med Ctr Utrecht, Dept Surg, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Radiol & Nucl Med, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Endocrine Oncol, Heidelberglaan 100, NL-3584 CX Utrecht, Netherlands
关键词:
Radioactive iodine-refractory differentiated thyroid carcinoma;
Prostate-specific membrane antigen;
Theranostic;
Gallium;
Lutetium;
PET;
CT;
MEMBRANE ANTIGEN-EXPRESSION;
PSMA EXPRESSION;
CARCINOMA;
GUIDELINES;
MANAGEMENT;
PAPILLARY;
THERAPY;
D O I:
10.1186/s13550-020-0610-x
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Background Differentiated thyroid carcinoma (DTC) is the most common type of thyroid cancer. Treatment with surgery, radioactive iodine (RAI), and TSH suppression is effective in most patients. Five to 15% of patients become RAI refractory and need alternative therapy; however, treatment options are limited. Ga-68-PSMA PET/CT, originally developed for prostate cancer, is also applicable to other malignancies, including thyroid carcinoma. The uptake of PSMA in thyroid carcinoma gives opportunities for imaging and therapy of RAI-refractory DTC. The aim of this study was to analyze imaging on Ga-68-PSMA PET/CT and evaluate the response to Lu-177-PSMA-617 therapy in patients with RAI-refractory DTC. Materials and methods Five patients with RAI-refractory DTC underwent Ga-68-PSMA PET/CT to determine their eligibility for Lu-177-PSMA-617 therapy. Ga-68-PSMA PET/CTs were analyzed visually and quantitatively. Response to Lu-177-PSMA-617 therapy was evaluated using imaging and thyroglobulin (Tg) values. Results Tracer uptake suspicious for distant metastases was depicted in all Ga-68-PSMA PET/CTs. Based on tracer uptake, three patients were eligible for Lu-177-PSMA-617 therapy, of whom two were treated. One patient showed disease progression on imaging 1 month later, while her Tg values gradually increased from 18 to 63 mu g/L in the months after treatment. Another patient showed partial, temporary response of lung and liver metastases. Her Tg levels initially decreased from 17 to 9 mu g/L. However, 7 months after treatment, there was disease progression on imaging and Tg levels had increased to 14 mu g/L. Imaging with Ga-68-PSMA PET/CT could be compared to (18)FDG PET/CT in three patients. Two patients showed additional lesions on Ga-68-PSMA PET/CT, and one patient showed concordant imaging. Conclusion Ga-68-PSMA PET/CT appears to have added value in patients with RAI-refractory DTC, as it is able to detect various types of lesions, some of which were not picked up by (18)FDG PET/CT. Furthermore, Ga-68-PSMA PET/CT might be used to identify patients eligible for treatment with Lu-177-PSMA-617. One of the two patients who underwent Lu-177-PSMA-617 therapy showed a modest, temporary response. To draw conclusions about the effectiveness of this therapy, more research is needed.
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