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Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma
PURPOSE: Glioblastoma (GBM) is the most common primary malignant brain tumor in adults. Despite the best available treatment, prognosis remains poor. Current standard therapy consists of surgical removal of the tumor followed by radiotherapy and chemotherapy with the alkylating agent temozolomide (T...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938624/ https://www.ncbi.nlm.nih.gov/pubmed/36803465 http://dx.doi.org/10.1186/s12883-023-03119-4 |
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author | Ehinger, Erik Kopecky, Jan Darabi, Anna Visse, Edward Edvardsson, Charlotte Tomasevic, Gregor Cederberg, David Belting, Mattias Bengzon, Johan Siesjö, Peter |
author_facet | Ehinger, Erik Kopecky, Jan Darabi, Anna Visse, Edward Edvardsson, Charlotte Tomasevic, Gregor Cederberg, David Belting, Mattias Bengzon, Johan Siesjö, Peter |
author_sort | Ehinger, Erik |
collection | PubMed |
description | PURPOSE: Glioblastoma (GBM) is the most common primary malignant brain tumor in adults. Despite the best available treatment, prognosis remains poor. Current standard therapy consists of surgical removal of the tumor followed by radiotherapy and chemotherapy with the alkylating agent temozolomide (TMZ). Experimental studies suggest that antisecretory factor (AF), an endogenous protein with proposed antisecretory and anti-inflammatory properties, may potentiate the effect of TMZ and alleviate cerebral edema. Salovum is an egg yolk powder enriched for AF and is classified as a medical food in the European Union. In this pilot study, we evaluate the safety and feasibility of add-on Salovum in GBM patients. METHODS: Eight patients with newly diagnosed, histologically confirmed GBM were prescribed Salovum during concomitant radiochemotherapy. Safety was determined by the number of treatment-related adverse events. Feasibility was determined by the number of patients who completed the full prescribed Salovum treatment. RESULTS: No serious treatment-related adverse events were observed. Out of 8 included patients, 2 did not complete the full treatment. Only one of the dropouts was due to issues directly related to Salovum, which were nausea and loss of appetite. Median survival was 23 months. CONCLUSIONS: We conclude that Salovum is safe to use as an add-on treatment for GBM. In terms of feasibility, adherence to the treatment regimen requires a determined and independent patient as the large doses prescribed may cause nausea and loss of appetite. TRIAL REGISTRATION: ClinicalTrials.gov NCT04116138. Registered on 04/10/2019. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-023-03119-4. |
format | Online Article Text |
id | pubmed-9938624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99386242023-02-19 Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma Ehinger, Erik Kopecky, Jan Darabi, Anna Visse, Edward Edvardsson, Charlotte Tomasevic, Gregor Cederberg, David Belting, Mattias Bengzon, Johan Siesjö, Peter BMC Neurol Research PURPOSE: Glioblastoma (GBM) is the most common primary malignant brain tumor in adults. Despite the best available treatment, prognosis remains poor. Current standard therapy consists of surgical removal of the tumor followed by radiotherapy and chemotherapy with the alkylating agent temozolomide (TMZ). Experimental studies suggest that antisecretory factor (AF), an endogenous protein with proposed antisecretory and anti-inflammatory properties, may potentiate the effect of TMZ and alleviate cerebral edema. Salovum is an egg yolk powder enriched for AF and is classified as a medical food in the European Union. In this pilot study, we evaluate the safety and feasibility of add-on Salovum in GBM patients. METHODS: Eight patients with newly diagnosed, histologically confirmed GBM were prescribed Salovum during concomitant radiochemotherapy. Safety was determined by the number of treatment-related adverse events. Feasibility was determined by the number of patients who completed the full prescribed Salovum treatment. RESULTS: No serious treatment-related adverse events were observed. Out of 8 included patients, 2 did not complete the full treatment. Only one of the dropouts was due to issues directly related to Salovum, which were nausea and loss of appetite. Median survival was 23 months. CONCLUSIONS: We conclude that Salovum is safe to use as an add-on treatment for GBM. In terms of feasibility, adherence to the treatment regimen requires a determined and independent patient as the large doses prescribed may cause nausea and loss of appetite. TRIAL REGISTRATION: ClinicalTrials.gov NCT04116138. Registered on 04/10/2019. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-023-03119-4. BioMed Central 2023-02-18 /pmc/articles/PMC9938624/ /pubmed/36803465 http://dx.doi.org/10.1186/s12883-023-03119-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ehinger, Erik Kopecky, Jan Darabi, Anna Visse, Edward Edvardsson, Charlotte Tomasevic, Gregor Cederberg, David Belting, Mattias Bengzon, Johan Siesjö, Peter Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
title | Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
title_full | Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
title_fullStr | Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
title_full_unstemmed | Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
title_short | Antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
title_sort | antisecretory factor is safe to use as add-on treatment in newly diagnosed glioblastoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938624/ https://www.ncbi.nlm.nih.gov/pubmed/36803465 http://dx.doi.org/10.1186/s12883-023-03119-4 |
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