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Neoadjuvant Systemic Treatment of Primary Angiosarcoma

Angiosarcoma is an extremely rare and aggressive malignancy. Standard of care of localized tumors includes surgery ± radiation. Despite this multimodal treatment, >50% of the angiosarcoma patients develop local or distant recurrent disease. The role of neoadjuvant systemic therapy is still contro...

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Autores principales: Heinhuis, Kimberley M., IJzerman, Nikki S., van der Graaf, Winette T. A., Kerst, Jan Martijn, Schrage, Yvonne, Beijnen, Jos H., Steeghs, Neeltje, van Houdt, Winan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464310/
https://www.ncbi.nlm.nih.gov/pubmed/32806524
http://dx.doi.org/10.3390/cancers12082251
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author Heinhuis, Kimberley M.
IJzerman, Nikki S.
van der Graaf, Winette T. A.
Kerst, Jan Martijn
Schrage, Yvonne
Beijnen, Jos H.
Steeghs, Neeltje
van Houdt, Winan J.
author_facet Heinhuis, Kimberley M.
IJzerman, Nikki S.
van der Graaf, Winette T. A.
Kerst, Jan Martijn
Schrage, Yvonne
Beijnen, Jos H.
Steeghs, Neeltje
van Houdt, Winan J.
author_sort Heinhuis, Kimberley M.
collection PubMed
description Angiosarcoma is an extremely rare and aggressive malignancy. Standard of care of localized tumors includes surgery ± radiation. Despite this multimodal treatment, >50% of the angiosarcoma patients develop local or distant recurrent disease. The role of neoadjuvant systemic therapy is still controversial and we therefore performed a systematic review of the literature to define the role of neoadjuvant systemic therapy based on available evidence. We focused on the effects of neoadjuvant systemic therapy on: 1. The success of surgical resection and 2. the long-term survival. All articles published before October 2019 on Ovid Medline, Ovid Embase, Cochrane library and Scopus were evaluated. Eighteen case reports and six retrospective cohort studies were included. There were no randomized controlled trials. This literature showed a beneficial role of neoadjuvant chemotherapy on downsizing of the tumor resulting in an improvement of the resection margins, especially in patients with cardiac or cutaneous angiosarcoma. However, no definitive conclusions on survival can be drawn based on the available literature lacking any prospective randomized studies in this setting. We advise that neoadjuvant chemotherapy should be considered, since this could lead to less mutilating resections and a higher rate of free resection margins. An international angiosarcoma registry could help to develop guidelines for this rare disease.
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spelling pubmed-74643102020-09-04 Neoadjuvant Systemic Treatment of Primary Angiosarcoma Heinhuis, Kimberley M. IJzerman, Nikki S. van der Graaf, Winette T. A. Kerst, Jan Martijn Schrage, Yvonne Beijnen, Jos H. Steeghs, Neeltje van Houdt, Winan J. Cancers (Basel) Review Angiosarcoma is an extremely rare and aggressive malignancy. Standard of care of localized tumors includes surgery ± radiation. Despite this multimodal treatment, >50% of the angiosarcoma patients develop local or distant recurrent disease. The role of neoadjuvant systemic therapy is still controversial and we therefore performed a systematic review of the literature to define the role of neoadjuvant systemic therapy based on available evidence. We focused on the effects of neoadjuvant systemic therapy on: 1. The success of surgical resection and 2. the long-term survival. All articles published before October 2019 on Ovid Medline, Ovid Embase, Cochrane library and Scopus were evaluated. Eighteen case reports and six retrospective cohort studies were included. There were no randomized controlled trials. This literature showed a beneficial role of neoadjuvant chemotherapy on downsizing of the tumor resulting in an improvement of the resection margins, especially in patients with cardiac or cutaneous angiosarcoma. However, no definitive conclusions on survival can be drawn based on the available literature lacking any prospective randomized studies in this setting. We advise that neoadjuvant chemotherapy should be considered, since this could lead to less mutilating resections and a higher rate of free resection margins. An international angiosarcoma registry could help to develop guidelines for this rare disease. MDPI 2020-08-12 /pmc/articles/PMC7464310/ /pubmed/32806524 http://dx.doi.org/10.3390/cancers12082251 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Heinhuis, Kimberley M.
IJzerman, Nikki S.
van der Graaf, Winette T. A.
Kerst, Jan Martijn
Schrage, Yvonne
Beijnen, Jos H.
Steeghs, Neeltje
van Houdt, Winan J.
Neoadjuvant Systemic Treatment of Primary Angiosarcoma
title Neoadjuvant Systemic Treatment of Primary Angiosarcoma
title_full Neoadjuvant Systemic Treatment of Primary Angiosarcoma
title_fullStr Neoadjuvant Systemic Treatment of Primary Angiosarcoma
title_full_unstemmed Neoadjuvant Systemic Treatment of Primary Angiosarcoma
title_short Neoadjuvant Systemic Treatment of Primary Angiosarcoma
title_sort neoadjuvant systemic treatment of primary angiosarcoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464310/
https://www.ncbi.nlm.nih.gov/pubmed/32806524
http://dx.doi.org/10.3390/cancers12082251
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