Gallium-68 prostate-specific membrane antigen ([68Ga]Ga-PSMA-11) PET for imaging of thyroid cancer: a feasibility study.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING EJNMMI Research Pub Date : 2020-10-22 DOI:10.1186/s13550-020-00720-3
Courtney Lawhn-Heath, Sue S Yom, Chienying Liu, Javier E Villanueva-Meyer, Maya Aslam, Raven Smith, Manpreet Narwal, Roxanna Juarez, Spencer C Behr, Miguel Hernandez Pampaloni, Jason W Chan, Christine M Glastonbury, Thomas A Hope, Robert R Flavell
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引用次数: 16

Abstract

Background: Prostate-specific membrane antigen (PSMA) is expressed in the microvasculature of thyroid cancer. This suggests the potential use of PSMA as a diagnostic agent in patients with aggressive forms of thyroid cancer. The purpose of the current study was to determine the feasibility and utility of [68Ga]Ga-PSMA-11 PET/MRI in thyroid cancer patients.

Methods: Eligible patients for this prospective pilot study were adults with a history of pathology-proven thyroid cancer who had abnormal radiotracer uptake on an 2-[18F]FDG PET and/or 131I scintigraphy performed in the 12 months prior to study enrollment. Patients underwent a [68Ga]Ga-PSMA-11 PET/MRI, and comparison was made to the prior qualifying 2-[18F]FDG PET CT/MRI for lesion location and relative intensity.

Results: Twelve patients underwent [68Ga]Ga-PSMA-11 PET/MRI, one of which was excluded from analysis due to debulking surgery prior to the PSMA PET. Of the remaining patients, 7/11 had differentiated disease (3 papillary, 2 follicular, 2 Hurthle cell) and 4/11 had dedifferentiated disease (2 poorly differentiated papillary, 2 anaplastic). Out of 43 lesions, 41 were visually 2-[18F]FDG positive (uptake greater than background, detection rate 95.3%) and 28 were PSMA positive (uptake greater than background, detection rate 65.1%). Uptake was heterogeneous between patients, and in some cases within patients. 3/11 patients (1 poorly differentiated papillary, 2 follicular) had PSMA uptake which was greater than FDG uptake. For the remaining 8 patients, 2-[18F]FDG uptake was greater than PSMA. Using one eligibility guideline in the prostate cancer literature for PSMA radioligand therapy (RLT), 8/11 could be considered eligible for possible future PSMA RLT. This was not predictable based on thyroid cancer subtype.

Conclusions: [68Ga]Ga-PSMA-11 PET demonstrated lower detection rate when compared to 2-[18F]FDG PET for thyroid cancer lesion visualization. Thyroid cancer subtype alone may not be sufficient to predict PSMA uptake, and radiotracer uptake may vary between patients and even within patients.

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镓-68前列腺特异性膜抗原([68Ga]Ga-PSMA-11) PET用于甲状腺癌显像的可行性研究
背景:前列腺特异性膜抗原(PSMA)在甲状腺癌的微血管中表达。这提示PSMA作为侵袭性甲状腺癌患者的诊断试剂的潜在用途。本研究的目的是确定[68Ga]Ga-PSMA-11 PET/MRI在甲状腺癌患者中的可行性和实用性。方法:这项前瞻性先导研究的合格患者是有病理证实的甲状腺癌病史的成年人,在研究入组前12个月进行2-[18F]FDG PET和/或131I显像检查时放射性示踪剂摄取异常。患者行[68Ga]Ga-PSMA-11 PET/MRI,并与先前合格的2-[18F]FDG PET CT/MRI进行病变位置和相对强度的比较。结果:12例患者接受了[68Ga]Ga-PSMA-11 PET/MRI检查,其中1例因在PSMA PET检查前进行了减体积手术而被排除在分析之外。其余患者中,7/11为分化病变(3例乳头状,2例滤泡,2例Hurthle细胞),4/11为去分化病变(2例低分化乳头状,2例间变性)。43例病灶中,41例2-[18F]FDG阳性(摄取大于背景,检出率95.3%),28例PSMA阳性(摄取大于背景,检出率65.1%)。患者之间的摄取是不均匀的,在某些情况下,患者内部也是如此。3/11患者(1例低分化乳头状,2例滤泡状)PSMA摄取大于FDG摄取。其余8例患者,2-[18F]FDG摄取大于PSMA。使用前列腺癌文献中PSMA放射配体治疗(RLT)的资格指南,8/11可以被认为有资格接受未来可能的PSMA RLT。基于甲状腺癌亚型,这是不可预测的。结论:与2-[18F]FDG PET相比,[68Ga]Ga-PSMA-11 PET对甲状腺癌病变的显像检出率较低。单独的甲状腺癌亚型可能不足以预测PSMA的摄取,放射性示踪剂的摄取可能在患者之间甚至患者内部有所不同。
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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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