PT - JOURNAL ARTICLE AU - Enke, Johanna S. AU - Ritzel, Kathrin AU - Asbach, Evelyn AU - Reitsam, Nic G. AU - Märkl, Bruno AU - Knösel, Thomas AU - Brüdgam, Denise AU - Kircher, Malte AU - Pfob, Christian H. AU - Bundschuh, Ralph A. AU - Rinscheid, Andreas AU - Nittbaur, Bernd AU - Wienand, Georgine AU - Schottelius, Margret AU - Reincke, Martin AU - Lapa, Constantin AU - Dierks, Alexander TI - C-X-C Motif Chemokine Receptor 4–Directed Scintigraphy Using [<sup>99m</sup>Tc]Tc-Pentixatec in Primary Aldosteronism: A Proof-of-Concept Study AID - 10.2967/jnumed.124.268169 DP - 2024 Oct 01 TA - Journal of Nuclear Medicine PG - 1640--1644 VI - 65 IP - 10 4099 - http://jnm.snmjournals.org/content/65/10/1640.short 4100 - http://jnm.snmjournals.org/content/65/10/1640.full SO - J Nucl Med2024 Oct 01; 65 AB - C-X-C motif chemokine receptor 4 (CXCR4)–directed imaging has gained clinical interest in aiding clinical diagnostics in primary aldosteronism (PA). We retrospectively evaluated the feasibility of CXCR4-directed scintigraphy using the novel CXCR-4 ligand [99mTc]Tc-pentixatec in patients with PA. Methods: Six patients (mean age ± SD, 49 ± 15 y) underwent CXCR4-directed scintigraphy (including planar imaging and SPECT/CT) 30, 120, and 240 min after injection of 435 ± 50 MBq of [99mTc]Tc-pentixatec. Adrenal CXCR4 expression was analyzed by calculating lesion-to-contralateral ratios (LCRs). Imaging results were correlated to clinical information. Histopathology and clinical follow-up served as the standard of reference. Results: Three subjects showed lateralization of adrenal tracer accumulation, with a mean maximum lesion-to-contralateral ratio of 1.65 (range, 1.52–1.70), which correlated with morphologic findings on CT. One individual underwent adrenalectomy and presented with complete biochemical and clinical remission at follow-up. Histopathologic workup confirmed unilateral aldosterone-producing adenoma. Conclusion: [99mTc]Tc-pentixatec scintigraphy with SPECT in patients with PA is feasible and might offer a valuable alternative to CXCR4-directed imaging with [68Ga]Ga-pentixafor PET.