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Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors
OBJECTIVES: This study aimed to evaluate the stability, safety, and efficacy of alpha-targeted therapy with [(225)Ac]Ac-DOTATATE in patients with grade 1/2 metastatic neuroendocrine tumors (NETs). METHODS: This retrospective cohort included patients (n=11) with metastatic NETs from different primary...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600558/ https://www.ncbi.nlm.nih.gov/pubmed/37870290 http://dx.doi.org/10.4274/mirt.galenos.2023.38258 |
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author | Demirci, Emre Alan Selçuk, Nalan Beydağı, Gamze Ocak, Meltem Toklu, Türkay Akçay, Kaan Kabasakal, Levent |
author_facet | Demirci, Emre Alan Selçuk, Nalan Beydağı, Gamze Ocak, Meltem Toklu, Türkay Akçay, Kaan Kabasakal, Levent |
author_sort | Demirci, Emre |
collection | PubMed |
description | OBJECTIVES: This study aimed to evaluate the stability, safety, and efficacy of alpha-targeted therapy with [(225)Ac]Ac-DOTATATE in patients with grade 1/2 metastatic neuroendocrine tumors (NETs). METHODS: This retrospective cohort included patients (n=11) with metastatic NETs from different primary sites (bronchial, pancreatic, nonpancreatic gastroenteropancreatic NETs, paraganglioma, and unknown primary site) treated with [(225)Ac]Ac-DOTATATE with a mean activity of 8.2±0.6 MBq (range: 7.5-10.0 MBq) at our institution between November 2019 and March 2022. The in vivo and in vitro stability of [(225)Ac]Ac-DOTATATE was calculated. The safety profile was evaluated according to the CTCAE-v5.0. Treatment efficacy was evaluated according to [(68)Ga] Ga-DOTATATE positron emission tomography/computed tomography (PET/CT) images and the RECIST 1.1 criteria. RESULTS: Patients had 73% (n=8) lymph node metastases, 91% (n=10) liver metastases, 36% (n=4) lung metastases, and 73% (n=8) bone metastases. All but one patient was refractory to treatment with [(177)Lu]Lu-DOTATATE. [(225)Ac]Ac-DOTATATE was stable for at least 5 h in vitro (in saline) and 3 h in vivo (urine and blood samples). Grade 2 renal toxicity and grade 2 hematotoxicity were observed in one patient. No grade 3-4 toxicities were reported. According to post-treatment [(68)Ga]Ga-DOTATATE PET/CT (n=9), 11% (n=1) had progressive disease, 44.4% (n=4) had stable disease, and 44.4% (n=4) had a partial response. The disease control rate was 89% (n=8). The median progression-free survival estimated according to Kaplan-Meier analysis was 12 months. CONCLUSION: The preliminary results of this study suggest that [(225)Ac]Ac-DOTATATE is stable, safe, and effective for treating advanced and [(177)Lu] Lu-DOTATATE-refractory NETs. However, prospective studies are needed to determine the impact of treatment on overall survival and to uncover potential side effects. |
format | Online Article Text |
id | pubmed-10600558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-106005582023-10-27 Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors Demirci, Emre Alan Selçuk, Nalan Beydağı, Gamze Ocak, Meltem Toklu, Türkay Akçay, Kaan Kabasakal, Levent Mol Imaging Radionucl Ther Original Article OBJECTIVES: This study aimed to evaluate the stability, safety, and efficacy of alpha-targeted therapy with [(225)Ac]Ac-DOTATATE in patients with grade 1/2 metastatic neuroendocrine tumors (NETs). METHODS: This retrospective cohort included patients (n=11) with metastatic NETs from different primary sites (bronchial, pancreatic, nonpancreatic gastroenteropancreatic NETs, paraganglioma, and unknown primary site) treated with [(225)Ac]Ac-DOTATATE with a mean activity of 8.2±0.6 MBq (range: 7.5-10.0 MBq) at our institution between November 2019 and March 2022. The in vivo and in vitro stability of [(225)Ac]Ac-DOTATATE was calculated. The safety profile was evaluated according to the CTCAE-v5.0. Treatment efficacy was evaluated according to [(68)Ga] Ga-DOTATATE positron emission tomography/computed tomography (PET/CT) images and the RECIST 1.1 criteria. RESULTS: Patients had 73% (n=8) lymph node metastases, 91% (n=10) liver metastases, 36% (n=4) lung metastases, and 73% (n=8) bone metastases. All but one patient was refractory to treatment with [(177)Lu]Lu-DOTATATE. [(225)Ac]Ac-DOTATATE was stable for at least 5 h in vitro (in saline) and 3 h in vivo (urine and blood samples). Grade 2 renal toxicity and grade 2 hematotoxicity were observed in one patient. No grade 3-4 toxicities were reported. According to post-treatment [(68)Ga]Ga-DOTATATE PET/CT (n=9), 11% (n=1) had progressive disease, 44.4% (n=4) had stable disease, and 44.4% (n=4) had a partial response. The disease control rate was 89% (n=8). The median progression-free survival estimated according to Kaplan-Meier analysis was 12 months. CONCLUSION: The preliminary results of this study suggest that [(225)Ac]Ac-DOTATATE is stable, safe, and effective for treating advanced and [(177)Lu] Lu-DOTATATE-refractory NETs. However, prospective studies are needed to determine the impact of treatment on overall survival and to uncover potential side effects. Galenos Publishing 2023-10 2023-10-20 /pmc/articles/PMC10600558/ /pubmed/37870290 http://dx.doi.org/10.4274/mirt.galenos.2023.38258 Text en ©Copyright 2023 by the Turkish Society of Nuclear Medicine / Molecular Imaging and Radionuclide Therapy published by Galenos Publishing House. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Demirci, Emre Alan Selçuk, Nalan Beydağı, Gamze Ocak, Meltem Toklu, Türkay Akçay, Kaan Kabasakal, Levent Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors |
title | Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors |
title_full | Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors |
title_fullStr | Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors |
title_full_unstemmed | Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors |
title_short | Initial Findings on the Use of [(225)Ac]Ac-DOTATATE Therapy as a Theranostic Application in Patients with Neuroendocrine Tumors |
title_sort | initial findings on the use of [(225)ac]ac-dotatate therapy as a theranostic application in patients with neuroendocrine tumors |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600558/ https://www.ncbi.nlm.nih.gov/pubmed/37870290 http://dx.doi.org/10.4274/mirt.galenos.2023.38258 |
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