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Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease
BACKGROUND: Von Hippel-Lindau (VHL) disease is a rare oncological disease with an incidence of 1:36,000, and is characterized by the growth of different types of tumours. Haemangioblastomas in the central nervous system (CNS) and retina, renal carcinoma and pheochromocytomas are the most common tumo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492903/ https://www.ncbi.nlm.nih.gov/pubmed/28662711 http://dx.doi.org/10.1186/s13023-017-0664-7 |
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author | Albiñana, Virginia Escribano, Rosa María Jiménez Soler, Isabel Padial, Luis Rodríguez Recio-Poveda, Lucia Villar Gómez de las Heras, Karina Botella, Luisa María |
author_facet | Albiñana, Virginia Escribano, Rosa María Jiménez Soler, Isabel Padial, Luis Rodríguez Recio-Poveda, Lucia Villar Gómez de las Heras, Karina Botella, Luisa María |
author_sort | Albiñana, Virginia |
collection | PubMed |
description | BACKGROUND: Von Hippel-Lindau (VHL) disease is a rare oncological disease with an incidence of 1:36,000, and is characterized by the growth of different types of tumours. Haemangioblastomas in the central nervous system (CNS) and retina, renal carcinoma and pheochromocytomas are the most common tumours. The absence of treatment for VHL leads to the need of repeated surgeries as the only option for these patients. Targeting VHL-derived tumours with drugs with reduced side effects is urgent to avoid repeated CNS surgeries. Recent reports have demonstrated that propranolol, a β-blocker used for the treatment of hypertension and other cardiac and neurological diseases, is the best option for infantile hemangioma (IH). Propranolol could be an efficient treatment to control haemangioblastoma growth in VHL disease given its antiangiogenic effects that were recently demonstrated by us. The main objective of the present study was the assessment of the efficacy and safety of propranolol on retinal haemangioblastoma in von Hippel-Lindau disease (VHL). METHODS: 7 VHL patients, from different regions of Spain, affected from juxtapapillary or peripheral haemangioblastomas were administered 120 mg propranolol daily. Patients were evaluated every 3 months for 12 months, at Virgen de la Salud Hospital (Toledo). The patients had juxtapapillary or peripheral haemangioblastomas but had refused standard treatments. RESULTS: Propranolol was initiated with a progressive increase up to a final dose of 120 mg daily. All tumours remained stable, and no new tumours appeared. The reabsorption of retinal exudation was noted in the two patients having exudates. No adverse effects were recorded. VEGF and miRNA 210 levels were monitored in the plasma of patients as possible biomarkers of VHL. These levels decreased in all cases from the first month of treatment. CONCLUSIONS: Although more studies are necessary, the results of this work suggest that propranolol is a drug to be considered in the treatment of VHL patients with retinal haemangioblastomas. VEGF and miRNA 210 could be used as biomarkers of the VHL disease activity. TRIAL REGISTRATION: The study has a clinical trial design and was registered at EU Clinical Trials Register and Spanish Clinical Studies Registry, EudraCT Number: 2014–003671-30. Registered 2 September 2014. |
format | Online Article Text |
id | pubmed-5492903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54929032017-06-30 Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease Albiñana, Virginia Escribano, Rosa María Jiménez Soler, Isabel Padial, Luis Rodríguez Recio-Poveda, Lucia Villar Gómez de las Heras, Karina Botella, Luisa María Orphanet J Rare Dis Research BACKGROUND: Von Hippel-Lindau (VHL) disease is a rare oncological disease with an incidence of 1:36,000, and is characterized by the growth of different types of tumours. Haemangioblastomas in the central nervous system (CNS) and retina, renal carcinoma and pheochromocytomas are the most common tumours. The absence of treatment for VHL leads to the need of repeated surgeries as the only option for these patients. Targeting VHL-derived tumours with drugs with reduced side effects is urgent to avoid repeated CNS surgeries. Recent reports have demonstrated that propranolol, a β-blocker used for the treatment of hypertension and other cardiac and neurological diseases, is the best option for infantile hemangioma (IH). Propranolol could be an efficient treatment to control haemangioblastoma growth in VHL disease given its antiangiogenic effects that were recently demonstrated by us. The main objective of the present study was the assessment of the efficacy and safety of propranolol on retinal haemangioblastoma in von Hippel-Lindau disease (VHL). METHODS: 7 VHL patients, from different regions of Spain, affected from juxtapapillary or peripheral haemangioblastomas were administered 120 mg propranolol daily. Patients were evaluated every 3 months for 12 months, at Virgen de la Salud Hospital (Toledo). The patients had juxtapapillary or peripheral haemangioblastomas but had refused standard treatments. RESULTS: Propranolol was initiated with a progressive increase up to a final dose of 120 mg daily. All tumours remained stable, and no new tumours appeared. The reabsorption of retinal exudation was noted in the two patients having exudates. No adverse effects were recorded. VEGF and miRNA 210 levels were monitored in the plasma of patients as possible biomarkers of VHL. These levels decreased in all cases from the first month of treatment. CONCLUSIONS: Although more studies are necessary, the results of this work suggest that propranolol is a drug to be considered in the treatment of VHL patients with retinal haemangioblastomas. VEGF and miRNA 210 could be used as biomarkers of the VHL disease activity. TRIAL REGISTRATION: The study has a clinical trial design and was registered at EU Clinical Trials Register and Spanish Clinical Studies Registry, EudraCT Number: 2014–003671-30. Registered 2 September 2014. BioMed Central 2017-06-29 /pmc/articles/PMC5492903/ /pubmed/28662711 http://dx.doi.org/10.1186/s13023-017-0664-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Albiñana, Virginia Escribano, Rosa María Jiménez Soler, Isabel Padial, Luis Rodríguez Recio-Poveda, Lucia Villar Gómez de las Heras, Karina Botella, Luisa María Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease |
title | Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease |
title_full | Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease |
title_fullStr | Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease |
title_full_unstemmed | Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease |
title_short | Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease |
title_sort | repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von hippel-lindau disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492903/ https://www.ncbi.nlm.nih.gov/pubmed/28662711 http://dx.doi.org/10.1186/s13023-017-0664-7 |
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