Cargando…

Somatostatin Receptor Theranostics for Refractory Meningiomas

Somatostatin receptor (SSTR)-targeted peptide receptor radionuclide therapy (PRRT) represents a promising approach for treatment-refractory meningiomas progressing after surgery and radiotherapy. The aim of this study was to provide outcomes of patients harboring refractory meningiomas treated by 17...

Descripción completa

Detalles Bibliográficos
Autores principales: Salgues, Betty, Graillon, Thomas, Horowitz, Tatiana, Chinot, Olivier, Padovani, Laetitia, Taïeb, David, Guedj, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406720/
https://www.ncbi.nlm.nih.gov/pubmed/36005176
http://dx.doi.org/10.3390/curroncol29080438
_version_ 1784774190021214208
author Salgues, Betty
Graillon, Thomas
Horowitz, Tatiana
Chinot, Olivier
Padovani, Laetitia
Taïeb, David
Guedj, Eric
author_facet Salgues, Betty
Graillon, Thomas
Horowitz, Tatiana
Chinot, Olivier
Padovani, Laetitia
Taïeb, David
Guedj, Eric
author_sort Salgues, Betty
collection PubMed
description Somatostatin receptor (SSTR)-targeted peptide receptor radionuclide therapy (PRRT) represents a promising approach for treatment-refractory meningiomas progressing after surgery and radiotherapy. The aim of this study was to provide outcomes of patients harboring refractory meningiomas treated by 177Lu-DOTATATE and an overall analysis of progression-free survival at 6 months (PFS-6) of the same relevant studies in the literature. Eight patients with recurrent and progressive WHO grade II meningiomas were treated after multimodal pretreatment with 177Lu-DOTATATE between 2019 and 2022. Primary and secondarily endpoints were progression-free survival at 6-months (PFS-6) and toxicity, respectively. PFS-6 analysis of our case series was compared with other similar relevant studies that included 86 patients treated with either 177Lu-DOTATATE or 90Y-DOTATOC. Our retrospective study showed a PFS-6 of 85.7% for WHO grade II progressive refractory meningiomas. Treatment was clinically and biologically well tolerated. The overall analysis of the previous relevant studies showed a PFS-6 of 89.7% for WHO grade I meningiomas (n = 29); 57.1% for WHO grade II (n = 21); and 0 % for WHO grade III (n = 12). For all grades (n = 86), including unknown grades, PFS-6 was 58.1%. SSTR-targeted PRRT allowed us to achieve prolonged PFS-6 in patients with WHO grade I and II progressive refractory meningiomas, except the most aggressive WHO grade II tumors. Large scale randomized trials are warranted for the better integration of PRRT in the treatment of refractory meningioma into clinical practice guidelines.
format Online
Article
Text
id pubmed-9406720
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-94067202022-08-26 Somatostatin Receptor Theranostics for Refractory Meningiomas Salgues, Betty Graillon, Thomas Horowitz, Tatiana Chinot, Olivier Padovani, Laetitia Taïeb, David Guedj, Eric Curr Oncol Article Somatostatin receptor (SSTR)-targeted peptide receptor radionuclide therapy (PRRT) represents a promising approach for treatment-refractory meningiomas progressing after surgery and radiotherapy. The aim of this study was to provide outcomes of patients harboring refractory meningiomas treated by 177Lu-DOTATATE and an overall analysis of progression-free survival at 6 months (PFS-6) of the same relevant studies in the literature. Eight patients with recurrent and progressive WHO grade II meningiomas were treated after multimodal pretreatment with 177Lu-DOTATATE between 2019 and 2022. Primary and secondarily endpoints were progression-free survival at 6-months (PFS-6) and toxicity, respectively. PFS-6 analysis of our case series was compared with other similar relevant studies that included 86 patients treated with either 177Lu-DOTATATE or 90Y-DOTATOC. Our retrospective study showed a PFS-6 of 85.7% for WHO grade II progressive refractory meningiomas. Treatment was clinically and biologically well tolerated. The overall analysis of the previous relevant studies showed a PFS-6 of 89.7% for WHO grade I meningiomas (n = 29); 57.1% for WHO grade II (n = 21); and 0 % for WHO grade III (n = 12). For all grades (n = 86), including unknown grades, PFS-6 was 58.1%. SSTR-targeted PRRT allowed us to achieve prolonged PFS-6 in patients with WHO grade I and II progressive refractory meningiomas, except the most aggressive WHO grade II tumors. Large scale randomized trials are warranted for the better integration of PRRT in the treatment of refractory meningioma into clinical practice guidelines. MDPI 2022-08-04 /pmc/articles/PMC9406720/ /pubmed/36005176 http://dx.doi.org/10.3390/curroncol29080438 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Salgues, Betty
Graillon, Thomas
Horowitz, Tatiana
Chinot, Olivier
Padovani, Laetitia
Taïeb, David
Guedj, Eric
Somatostatin Receptor Theranostics for Refractory Meningiomas
title Somatostatin Receptor Theranostics for Refractory Meningiomas
title_full Somatostatin Receptor Theranostics for Refractory Meningiomas
title_fullStr Somatostatin Receptor Theranostics for Refractory Meningiomas
title_full_unstemmed Somatostatin Receptor Theranostics for Refractory Meningiomas
title_short Somatostatin Receptor Theranostics for Refractory Meningiomas
title_sort somatostatin receptor theranostics for refractory meningiomas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406720/
https://www.ncbi.nlm.nih.gov/pubmed/36005176
http://dx.doi.org/10.3390/curroncol29080438
work_keys_str_mv AT salguesbetty somatostatinreceptortheranosticsforrefractorymeningiomas
AT graillonthomas somatostatinreceptortheranosticsforrefractorymeningiomas
AT horowitztatiana somatostatinreceptortheranosticsforrefractorymeningiomas
AT chinotolivier somatostatinreceptortheranosticsforrefractorymeningiomas
AT padovanilaetitia somatostatinreceptortheranosticsforrefractorymeningiomas
AT taiebdavid somatostatinreceptortheranosticsforrefractorymeningiomas
AT guedjeric somatostatinreceptortheranosticsforrefractorymeningiomas