[<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...
Saved in:
Main Authors: | , , , , , , , , , , , |
---|---|
Format: | Book |
Published: |
MDPI AG,
2023-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
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 |