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Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol

Radio-ligand therapy (RLT) with(177)Lu-PSMA-617 is a promising option for patients with metastatic castration-resistant prostate-cancer (mCRPC). A prospective phase-II study (EUDRACT/RSO,2016-002732-32) on mCRPC is ongoing at IRST (Meldola, Italy). A total of 9 patients (median age: 68 y, range: 53–...

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Autores principales: Sarnelli, Anna, Belli, Maria Luisa, Di Iorio, Valentina, Mezzenga, Emilio, Celli, Monica, Severi, Stefano, Tardelli, Elisa, Nicolini, Silvia, Oboldi, Devil, Uccelli, Licia, Cittanti, Corrado, Monti, Manuela, Ferrari, Mahila, Paganelli, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385027/
https://www.ncbi.nlm.nih.gov/pubmed/30754620
http://dx.doi.org/10.3390/molecules24030621
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author Sarnelli, Anna
Belli, Maria Luisa
Di Iorio, Valentina
Mezzenga, Emilio
Celli, Monica
Severi, Stefano
Tardelli, Elisa
Nicolini, Silvia
Oboldi, Devil
Uccelli, Licia
Cittanti, Corrado
Monti, Manuela
Ferrari, Mahila
Paganelli, Giovanni
author_facet Sarnelli, Anna
Belli, Maria Luisa
Di Iorio, Valentina
Mezzenga, Emilio
Celli, Monica
Severi, Stefano
Tardelli, Elisa
Nicolini, Silvia
Oboldi, Devil
Uccelli, Licia
Cittanti, Corrado
Monti, Manuela
Ferrari, Mahila
Paganelli, Giovanni
author_sort Sarnelli, Anna
collection PubMed
description Radio-ligand therapy (RLT) with(177)Lu-PSMA-617 is a promising option for patients with metastatic castration-resistant prostate-cancer (mCRPC). A prospective phase-II study (EUDRACT/RSO,2016-002732-32) on mCRPC is ongoing at IRST (Meldola, Italy). A total of 9 patients (median age: 68 y, range: 53–85) were enrolled for dosimetry evaluation of parotid glands (PGs), kidneys, red marrow (RM) and whole body (WB). Folic polyglutamate tablets were orally administered as PGs protectors and 500 mL of a 10% mannitol solution was intravenously infused to reduce kidney uptake. The whole body planar image (WBI) and blood samples were acquired at different times post infusion (1 h, 16–24 h, 36–48 h and 120 h). Dose calculation was performed with MIRD formalism (OLINDA/EXM software). The median effective half-life was 33.0 h (range: 25.6–60.7) for PGs, 31.4 h (12.2–80.6) for kidneys, 8.2 h (2.5–14.7) for RM and 40.1 h (31.6–79.7) for WB. The median doses were 0.48 mGy/MBq (range: 0.33–2.63) for PGs, 0.70 mGy/MBq (0.26–1.07) for kidneys, 0.044 mGy/MBq (0.023–0.067) for RM and 0.04 mGy/MBq (0.02–0.11) for WB. A comparison with previously published dosimetric data was performed and a significant difference was found for PGs while no significant difference was observed for the kidneys. For PGs, the possibility of reducing uptake by administering glutamate tablets during RLT seems feasible while further research is warranted for a more focused evaluation of the reduction in kidney uptake.
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spelling pubmed-63850272019-02-23 Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol Sarnelli, Anna Belli, Maria Luisa Di Iorio, Valentina Mezzenga, Emilio Celli, Monica Severi, Stefano Tardelli, Elisa Nicolini, Silvia Oboldi, Devil Uccelli, Licia Cittanti, Corrado Monti, Manuela Ferrari, Mahila Paganelli, Giovanni Molecules Article Radio-ligand therapy (RLT) with(177)Lu-PSMA-617 is a promising option for patients with metastatic castration-resistant prostate-cancer (mCRPC). A prospective phase-II study (EUDRACT/RSO,2016-002732-32) on mCRPC is ongoing at IRST (Meldola, Italy). A total of 9 patients (median age: 68 y, range: 53–85) were enrolled for dosimetry evaluation of parotid glands (PGs), kidneys, red marrow (RM) and whole body (WB). Folic polyglutamate tablets were orally administered as PGs protectors and 500 mL of a 10% mannitol solution was intravenously infused to reduce kidney uptake. The whole body planar image (WBI) and blood samples were acquired at different times post infusion (1 h, 16–24 h, 36–48 h and 120 h). Dose calculation was performed with MIRD formalism (OLINDA/EXM software). The median effective half-life was 33.0 h (range: 25.6–60.7) for PGs, 31.4 h (12.2–80.6) for kidneys, 8.2 h (2.5–14.7) for RM and 40.1 h (31.6–79.7) for WB. The median doses were 0.48 mGy/MBq (range: 0.33–2.63) for PGs, 0.70 mGy/MBq (0.26–1.07) for kidneys, 0.044 mGy/MBq (0.023–0.067) for RM and 0.04 mGy/MBq (0.02–0.11) for WB. A comparison with previously published dosimetric data was performed and a significant difference was found for PGs while no significant difference was observed for the kidneys. For PGs, the possibility of reducing uptake by administering glutamate tablets during RLT seems feasible while further research is warranted for a more focused evaluation of the reduction in kidney uptake. MDPI 2019-02-11 /pmc/articles/PMC6385027/ /pubmed/30754620 http://dx.doi.org/10.3390/molecules24030621 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sarnelli, Anna
Belli, Maria Luisa
Di Iorio, Valentina
Mezzenga, Emilio
Celli, Monica
Severi, Stefano
Tardelli, Elisa
Nicolini, Silvia
Oboldi, Devil
Uccelli, Licia
Cittanti, Corrado
Monti, Manuela
Ferrari, Mahila
Paganelli, Giovanni
Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol
title Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol
title_full Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol
title_fullStr Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol
title_full_unstemmed Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol
title_short Dosimetry of (177)Lu-PSMA-617 after Mannitol Infusion and Glutamate Tablet Administration: Preliminary Results of EUDRACT/RSO 2016-002732-32 IRST Protocol
title_sort dosimetry of (177)lu-psma-617 after mannitol infusion and glutamate tablet administration: preliminary results of eudract/rso 2016-002732-32 irst protocol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385027/
https://www.ncbi.nlm.nih.gov/pubmed/30754620
http://dx.doi.org/10.3390/molecules24030621
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