A Phase I/IIa Clinical Trial to Evaluate Safety and Adrenal Uptake of Para-Chloro-2-[<sup>18</sup>F]Fluoroethyletomidate in Healthy Volunteers and Patients with Primary Aldosteronism.
Level II
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- Record sourced from PubMed, PMID 39884776.
- Also identified by DOI 10.2967/jnumed.124.268425.
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Abstract
Primary aldosteronism (PA) is a common, potentially reversible, cause of hypertension. Distinguishing unilateral from bilateral PA is critical when deciding who should be offered surgery (unilateral adrenalectomy). Recent studies have shown that PET/CT with [<sup>11</sup>C]metomidate can accurately identify unilateral PA, with localization of the causative aldosterone-producing adenoma (APA). However, the availability of [<sup>11</sup>C]metomidate is limited to centers with an on-site cyclotron. Here, we report an early-phase human study with the <sup>18</sup>F-labeled analog, para-chloro-2-[<sup>18</sup>F]fluoroethyletomidate ([<sup>18</sup>F]CETO). <b>Methods:</b> We conducted a phase I/IIa, single-center, open-label, microdosing study. The primary objective was to evaluate the safety of up to 2 administrations of [<sup>18</sup>F]CETO in 6 patients with PA (3 unilateral disease, 3 bilateral disease) and 5 healthy volunteers. Safety evaluation included assessment of adrenal function after the first [<sup>18</sup>F]CETO administration. The biodistribution of [<sup>18</sup>F]CETO was assessed in a 90-min dynamic PET acquisition. In patients with PA, the effect of pretreatment with oral dexamethasone on [<sup>18</sup>F]CETO uptake by normal adrenal tissue and APAs was also assessed. <b>Results:</b> Eleven participants were recruited to the trial, including 6 patients and 5 healthy volunteers. No subjects experienced serious adverse events or reactions, and all participants had normal adrenal function after [<sup>18</sup>F]CETO administration. [<sup>18</sup>F]CETO demonstrated high selectivity for the adrenal glands with low uptake in other tissues. Visualization of APAs was enhanced after dexamethasone pretreatment, which suppressed [<sup>18</sup>F]CETO uptake by normal adrenal tissue. <b>Conclusion:</b> [<sup>18</sup>F]CETO is a safe radiopharmaceutical for PET imaging of the adrenal glands, with no observed adverse reactions or impairment of adrenal function in this study. [<sup>18</sup>F]CETO demonstrates selective high affinity for adrenal tissue, particularly APAs. Distinction between APAs and normal adrenal tissue is enhanced by dexamethasone pretreatment to suppress [<sup>18</sup>F]CETO uptake by normal glands. This positions [<sup>18</sup>F]CETO as a promising imaging tool for evaluation in the context of PA.
Medical subject headings
- Hyperaldosteronism
- Etomidate
- Adrenal Glands
- Safety