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PSMA PET/CT Identifies Intrapatient Variation in Salivary Gland Toxicity From Iodine-131 Therapy.
Molecular Imaging ( IF 2.8 ) Pub Date : 2020-07-03 , DOI: 10.1177/1536012120934992
Vineet Mohan 1, 2 , Wouter V Vogel 1, 2 , Gerlof D Valk 3 , Jan P de Boer 4 , Marnix G E H Lam 5 , Bart de Keizer 5
Affiliation  

Introduction:

Xerostomia is a well-known complication after iodine-131 (131I) therapy for thyroid carcinoma. It is currently insufficiently understood how the dose and biodistribution of 131I relates to salivary gland toxicity, and whether this is consistent for all salivary glands within a single patient. Prostate-specific membrane antigen (PSMA) positron emission tomography/computed tomography (PET/CT) was recently introduced as a new tool to evaluate the relative loss of vital acinar cells in individual salivary glands. We aimed to assess gland-specific salivary gland toxicity after 131I-therapy using PSMA PET/CT.

Methods:

Five patients with differentiated thyroid cancer underwent [68Ga]Ga-PSMA-11 PET/CT to evaluate their eligibility for peptide radioligand therapy with [177Lu]Lu-PSMA-617. Uptake patterns in salivary glands were evaluated visually and quantitatively as an indicator of vital acinar cell loss after prior 131I-therapy.

Results:

Four of 5 patients demonstrated significant lowered uptake in at least one salivary gland, after receiving at least 2 131I-treatments. Asymmetric loss of vital acinar cells occurred by gland type (parotid/submandibular) and location (right/left). The other salivary glands in these patients and all salivary glands in the fifth patient showed normal uptake, demonstrating high intrapatient and interpatient variability.

Conclusions:

131I-therapy can induce salivary gland toxicity with high inter- but also high intrapatient variation among separate gland locations, which can be assessed with PSMA PET/CT. This new technique offers potential to guide further development and evaluation of protective measures in patients receiving 131I-therapy.



中文翻译:

PSMA PET / CT可以从碘131治疗中识别出患者唾液腺毒性的变异。

介绍:

口腔干燥症是碘131(131 I)治疗甲状腺癌后的众所周知的并发症。目前尚不充分了解131 I的剂量和生物分布与唾液腺毒性之间的关系,以及对于单个患者中所有唾液腺是否一致。最近引入了前列腺特异性膜抗原(PSMA)正电子发射断层扫描/计算机断层扫描(PET / CT)作为评估个体唾液腺中重要腺泡细胞相对损失的新工具。我们旨在评估使用PSMA PET / CT进行131 I治疗后特定腺体唾液腺的毒性。

方法:

对5例分化型甲状腺癌患者进行了[ 68 Ga] Ga-PSMA-11 PET / CT,以评估他们接受[ 177 Lu] Lu-PSMA-617进行肽放射配体治疗的资格。视觉和定量评估唾液腺的摄取模式,作为先前131 I治疗后重要腺泡细胞损失的指标。

结果:

5名患者中有4在接受至少2 131 I治疗后,至少一个唾液腺的摄取明显降低。腺泡类型(腮腺/下颌下颌)和位置(右/左)引起重要腺泡细胞的不对称损失。这些患者的其他唾液腺和第五位患者的所有唾液腺均显示正常摄取,表明患者内和患者间差异很大。

结论:

131 I治疗可以诱发唾液腺毒性,在不同的腺体部位之间存在较高的患者间差异,而且患者内部差异很大,可以使用PSMA PET / CT进行评估。这项新技术为指导接受131 I治疗的患者的进一步开发和评估保护措施提供了潜力。

更新日期:2020-07-03
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