[<sup>111</sup>In]In/[<sup>177</sup>Lu]Lu-AAZTA<sup>5</sup>-LM4 SST<sub>2</sub>R-Antagonists in Cancer Theranostics: From Preclinical Testing to First Patient Results

Aiming to expand the application of the SST<sub>2</sub>R-antagonist LM4 (DPhe-c[DCys-4Pal-DAph(Cbm)-Lys-Thr-Cys]-DTyr-NH<sub>2</sub>) beyond [<sup>68</sup>Ga]Ga-DATA<sup>5m</sup>-LM4 PET/CT (DATA<sup>5m</sup>, (6-pentanoic acid)-6-(amino)me...

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Main Authors: Berthold A. Nock (Author), Panagiotis Kanellopoulos (Author), Euy Sung Moon (Author), Maritina Rouchota (Author), George Loudos (Author), Sanjana Ballal (Author), Madhav P. Yadav (Author), Chandrasekhar Bal (Author), Prashant Mishra (Author), Parvind Sheokand (Author), Frank Roesch (Author), Theodosia Maina (Author)
Format: Book
Published: MDPI AG, 2023-02-01T00:00:00Z.
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Summary:Aiming to expand the application of the SST<sub>2</sub>R-antagonist LM4 (DPhe-c[DCys-4Pal-DAph(Cbm)-Lys-Thr-Cys]-DTyr-NH<sub>2</sub>) beyond [<sup>68</sup>Ga]Ga-DATA<sup>5m</sup>-LM4 PET/CT (DATA<sup>5m</sup>, (6-pentanoic acid)-6-(amino)methy-1,4-diazepinetriacetate), we now introduce AAZTA<sup>5</sup>-LM4 (AAZTA<sup>5</sup>, 1,4-bis(carboxymethyl)-6-[bis(carboxymethyl)]amino-6-[pentanoic-acid]perhydro-1,4-diazepine), allowing for the convenient coordination of trivalent radiometals of clinical interest, such as In-111 (for SPECT/CT) or Lu-177 (for radionuclide therapy). After labeling, the preclinical profiles of [<sup>111</sup>In]In-AAZTA<sup>5</sup>-LM4 and [<sup>177</sup>Lu]Lu-AAZTA<sup>5</sup>-LM4 were compared in HEK293-SST<sub>2</sub>R cells and double HEK293-SST<sub>2</sub>R/wtHEK293 tumor-bearing mice using [<sup>111</sup>In]In-DOTA-LM3 and [<sup>177</sup>Lu]Lu-DOTA-LM3 as references. The biodistribution of [<sup>177</sup>Lu]Lu-AAZTA<sup>5</sup>-LM4 was additionally studied for the first time in a NET patient. Both [<sup>111</sup>In]In-AAZTA<sup>5</sup>-LM4 and [<sup>177</sup>Lu]Lu-AAZTA<sup>5</sup>-LM4 displayed high and selective targeting of the HEK293-SST<sub>2</sub>R tumors in mice and fast background clearance via the kidneys and the urinary system. This pattern was reproduced for [<sup>177</sup>Lu]Lu-AAZTA<sup>5</sup>-LM4 in the patient according to SPECT/CT results in a monitoring time span of 4-72 h pi. In view of the above, we may conclude that [<sup>177</sup>Lu]Lu-AAZTA<sup>5</sup>-LM4 shows promise as a therapeutic radiopharmaceutical candidate for SST<sub>2</sub>R-expressing human NETs, based on previous [<sup>68</sup>Ga]Ga-DATA<sup>5m</sup>-LM4 PET/CT, but further studies are needed to fully assess its clinical value. Furthermore, [<sup>111</sup>In]In-AAZTA<sup>5</sup>-LM4 SPECT/CT may represent a legitimate alternative diagnostic option in cases where PET/CT is not available.
Item Description:10.3390/pharmaceutics15030776
1999-4923