Van den Broeck Bliede, Debacker Jens M, Bauters Wouter, Creytens David, Ferdinande Liesbeth, Huvenne Wouter, Lapauw Bruno, Schelfhout Vanessa, Van Laeken Nick, Verroken Charlotte
Department of Medical Imaging, Nuclear Medicine, Ghent University Hospital, C. Heymanslaan 10, 9000, Ghent, Belgium.
Molecular Imaging and Therapy Research Group (MITH), Vrije Universiteit Brussel (VUB), Brussels, Belgium.
EJNMMI Res. 2024 Sep 12;14(1):82. doi: 10.1186/s13550-024-01148-9.
Patients diagnosed with radioiodine refractory (RAI-R) thyroid carcinoma (TC) have a significantly worse prognosis than patients with radiosensitive TC. These refractory malignancies are often dedifferentiated, hindering the effectiveness of iodine-based imaging. Additionally, the role of metabolic imaging using [F]FDG PET/CT is also limited in these cases, making adequate staging of RAI-R TC challenging. Recent case series have shown promising results regarding the role of the prostate-specific membrane antigen (PSMA) in TC. In this study we explored the value of [F]AlF-PSMA-11 PET/CT in RAI-R TC.
In this phase II study, lesions detected on [F]AlF-PSMA-11 PET were compared to findings from [F]FDG PET/CT. Additionally, the serologic soluble prostate-specific membrane antigen (sPSMA) was measured using ELISA. PSMA-expression on tumor tissue in any available resection specimens was analysed with an immunostainer.
Eight patients were included, with a total of 39 identified lesions based on PET imaging. [F]AlF-PSMA-11 PET identified 30 of 39 lesions, and [F]FDG PET identified 33 lesions, leading to a detection rate of 76.9% and 84.6%, respectively. Interestingly, while nine lesions were solely visualized on [F]FDG, six were uniquely seen on [F]AlF-PSMA-11 PET. While sPSMA was immeasurable in all female patients, no correlation was found between sPSMA in male patients and disease-related factors. In five out of eight patients immunohistology showed PSMA expression on the primary tumor.
Although not all lesions could be visualized, [F]PSMA-11 PET identified multiple lesions imperceptible on [F]FDG PET. These results display the potential additional diagnostic role of PSMA-targeted imaging in patients with RAI-R TC. Trial registration number No. EudraCT 2021-000456-19.
与放射性碘敏感的甲状腺癌(TC)患者相比,被诊断为放射性碘难治性(RAI-R)甲状腺癌的患者预后明显更差。这些难治性恶性肿瘤通常发生去分化,影响基于碘的成像效果。此外,在这些病例中,使用[F]FDG PET/CT进行代谢成像的作用也有限,这使得对RAI-R TC进行充分分期具有挑战性。最近的病例系列研究显示,前列腺特异性膜抗原(PSMA)在TC中的作用有令人鼓舞的结果。在本研究中,我们探讨了[F]AlF-PSMA-11 PET/CT在RAI-R TC中的价值。
在这项II期研究中,将[F]AlF-PSMA-11 PET检测到的病变与[F]FDG PET/CT的结果进行比较。此外,使用酶联免疫吸附测定法(ELISA)测量血清可溶性前列腺特异性膜抗原(sPSMA)。用免疫染色剂分析任何可用切除标本中肿瘤组织上的PSMA表达。
纳入8例患者,基于PET成像共识别出39个病变。[F]AlF-PSMA-11 PET识别出39个病变中的30个,[F]FDG PET识别出33个病变,检测率分别为76.9%和84.6%。有趣的是,虽然9个病变仅在[F]FDG上可见,但6个病变仅在[F]AlF-PSMA-11 PET上可见。虽然所有女性患者的sPSMA均无法测量,但未发现男性患者的sPSMA与疾病相关因素之间存在相关性。8例患者中有5例免疫组织化学显示原发性肿瘤上有PSMA表达。
尽管并非所有病变都能被可视化,但[F]PSMA-11 PET识别出了多个在[F]FDG PET上无法察觉的病变。这些结果显示了PSMA靶向成像在RAI-R TC患者中的潜在额外诊断作用。试验注册号:EudraCT 2021-000456-19。