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Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions

Transhepatic radionuclide infusion has been introduced as a new treatment approach for unresectable liver neuroendocrine metastatic lesions with the prerequisite of a positive In-111 Pentetreotide (Octreoscan). Patients with multiple liver neuroendocrine metastases can be locally treated after selec...

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Autor principal: Limouris, Georgios S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356116/
https://www.ncbi.nlm.nih.gov/pubmed/22655264
http://dx.doi.org/10.3389/fonc.2012.00020
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author Limouris, Georgios S.
author_facet Limouris, Georgios S.
author_sort Limouris, Georgios S.
collection PubMed
description Transhepatic radionuclide infusion has been introduced as a new treatment approach for unresectable liver neuroendocrine metastatic lesions with the prerequisite of a positive In-111 Pentetreotide (Octreoscan). Patients with multiple liver neuroendocrine metastases can be locally treated after selective hepatic artery catheterization and infusion of radiolabeled somatostatin analogs, and in case of extra-hepatic secondary spread, after simple i.v. application. According to the world wide references, the average dose per session to each patient is 6.3 ± 0.3 GBq (∼160–180 mCi) of In-111-DTPA-Phe1-Pentetreotide, 10- to 12-fold in total, administered monthly or of 4.1 ± 0.2 GBq (∼105–116 mCi) of Y-90 DOTA TOC, threefold in total, or of 7.0 ± 0.4 GBq (∼178–200 mCi) of Lu-177 DOTA TATE, fourfold to sixfold in total (the choice of which being based on the tumor size, assessed by CT or MRI). Follow-up at monthly intervals has to be performed by means of ultrasonography (US). Treatment response has to be assessed according to the WHO criteria (RECIST or SWOG).
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spelling pubmed-33561162012-05-31 Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions Limouris, Georgios S. Front Oncol Oncology Transhepatic radionuclide infusion has been introduced as a new treatment approach for unresectable liver neuroendocrine metastatic lesions with the prerequisite of a positive In-111 Pentetreotide (Octreoscan). Patients with multiple liver neuroendocrine metastases can be locally treated after selective hepatic artery catheterization and infusion of radiolabeled somatostatin analogs, and in case of extra-hepatic secondary spread, after simple i.v. application. According to the world wide references, the average dose per session to each patient is 6.3 ± 0.3 GBq (∼160–180 mCi) of In-111-DTPA-Phe1-Pentetreotide, 10- to 12-fold in total, administered monthly or of 4.1 ± 0.2 GBq (∼105–116 mCi) of Y-90 DOTA TOC, threefold in total, or of 7.0 ± 0.4 GBq (∼178–200 mCi) of Lu-177 DOTA TATE, fourfold to sixfold in total (the choice of which being based on the tumor size, assessed by CT or MRI). Follow-up at monthly intervals has to be performed by means of ultrasonography (US). Treatment response has to be assessed according to the WHO criteria (RECIST or SWOG). Frontiers Research Foundation 2012-02-28 /pmc/articles/PMC3356116/ /pubmed/22655264 http://dx.doi.org/10.3389/fonc.2012.00020 Text en Copyright © 2012 Limouris. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Oncology
Limouris, Georgios S.
Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions
title Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions
title_full Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions
title_fullStr Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions
title_full_unstemmed Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions
title_short Neuroendocrine Tumors: A Focus on Liver Metastatic Lesions
title_sort neuroendocrine tumors: a focus on liver metastatic lesions
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356116/
https://www.ncbi.nlm.nih.gov/pubmed/22655264
http://dx.doi.org/10.3389/fonc.2012.00020
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