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Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology
BACKGROUND: Angiosarcomas are rare and heterogeneous tumors with poor prognosis. The clinical subtypes are classified depending on the primary site and etiology. METHODS: We conducted a retrospective, monocentric study of 136 patients with localized AS between May 1985 and November 2018. Overall sur...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449723/ https://www.ncbi.nlm.nih.gov/pubmed/34545273 http://dx.doi.org/10.1155/2021/9960085 |
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author | Schott, Inna Liffers, Sven-Thorsten Farzaliyev, Farhad Falkenhorst, Johanna Steinau, Hans-Ulrich Treckmann, Jürgen-Walter Podleska, Lars Erik Pöttgen, Christoph Schildhaus, Hans-Ulrich Ahrens, Marit Dirksen, Uta Murat, Fatma-Zehra Siveke, Jens T. Bauer, Sebastian Hamacher, Rainer |
author_facet | Schott, Inna Liffers, Sven-Thorsten Farzaliyev, Farhad Falkenhorst, Johanna Steinau, Hans-Ulrich Treckmann, Jürgen-Walter Podleska, Lars Erik Pöttgen, Christoph Schildhaus, Hans-Ulrich Ahrens, Marit Dirksen, Uta Murat, Fatma-Zehra Siveke, Jens T. Bauer, Sebastian Hamacher, Rainer |
author_sort | Schott, Inna |
collection | PubMed |
description | BACKGROUND: Angiosarcomas are rare and heterogeneous tumors with poor prognosis. The clinical subtypes are classified depending on the primary site and etiology. METHODS: We conducted a retrospective, monocentric study of 136 patients with localized AS between May 1985 and November 2018. Overall survival (OS), local recurrence-free survival (LRFS), and metastasis-free survival (MFS) were estimated using the Kaplan–Meier method. To identify prognostic factors, univariate and multivariate analyses were performed based on Cox regressions. RESULTS: The median age was 67 years (19–72.8 years). Primary sites were cutaneous (27.2%), breast (38.2%), and deep soft tissue (34.6%). The majority was primary angiosarcomas (55.9%) followed by postradiation (40.4%) and chronic lymphedema angiosarcomas (2.9%). Prognosis significantly differed depending on the primary site and etiology. Shortest median OS and MFS were observed in deep soft tissue angiosarcomas, whereas cutaneous angiosarcomas, angiosarcomas of the breast, and radiation-associated angiosarcomas displayed worse median LRFS. Univariate analyses showed better OS for tumor size <10 cm (p = 0.009), negative surgical margins (p = 0.021), and negative lymph node status (p = 0.007). LRFS and MFS were longer for tumor size <10 cm (p = 0.012 and p = 0.013). In multivariate analyses, age <70 years was the only independent positive prognostic factor for OS in all subgroups. For LRFS, secondary AS of the breast was a negative prognostic factor (HR: 2.35; p = 0.035). CONCLUSIONS: Different behaviors and prognoses depending on the primary site and etiology should be considered for the treatment of this heterogeneous disease. In cutaneous angiosarcomas of the head/neck and postradiation angiosarcomas of the breast, local recurrence seems to have a crucial impact on OS. Therefore, improved local therapies and local tumor staging may have to be implemented. However, in deep soft tissue angiosarcomas, distant recurrence seems to have a major influence on prognosis, which indicates a benefit of additional perioperative chemotherapy. |
format | Online Article Text |
id | pubmed-8449723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-84497232021-09-19 Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology Schott, Inna Liffers, Sven-Thorsten Farzaliyev, Farhad Falkenhorst, Johanna Steinau, Hans-Ulrich Treckmann, Jürgen-Walter Podleska, Lars Erik Pöttgen, Christoph Schildhaus, Hans-Ulrich Ahrens, Marit Dirksen, Uta Murat, Fatma-Zehra Siveke, Jens T. Bauer, Sebastian Hamacher, Rainer Sarcoma Research Article BACKGROUND: Angiosarcomas are rare and heterogeneous tumors with poor prognosis. The clinical subtypes are classified depending on the primary site and etiology. METHODS: We conducted a retrospective, monocentric study of 136 patients with localized AS between May 1985 and November 2018. Overall survival (OS), local recurrence-free survival (LRFS), and metastasis-free survival (MFS) were estimated using the Kaplan–Meier method. To identify prognostic factors, univariate and multivariate analyses were performed based on Cox regressions. RESULTS: The median age was 67 years (19–72.8 years). Primary sites were cutaneous (27.2%), breast (38.2%), and deep soft tissue (34.6%). The majority was primary angiosarcomas (55.9%) followed by postradiation (40.4%) and chronic lymphedema angiosarcomas (2.9%). Prognosis significantly differed depending on the primary site and etiology. Shortest median OS and MFS were observed in deep soft tissue angiosarcomas, whereas cutaneous angiosarcomas, angiosarcomas of the breast, and radiation-associated angiosarcomas displayed worse median LRFS. Univariate analyses showed better OS for tumor size <10 cm (p = 0.009), negative surgical margins (p = 0.021), and negative lymph node status (p = 0.007). LRFS and MFS were longer for tumor size <10 cm (p = 0.012 and p = 0.013). In multivariate analyses, age <70 years was the only independent positive prognostic factor for OS in all subgroups. For LRFS, secondary AS of the breast was a negative prognostic factor (HR: 2.35; p = 0.035). CONCLUSIONS: Different behaviors and prognoses depending on the primary site and etiology should be considered for the treatment of this heterogeneous disease. In cutaneous angiosarcomas of the head/neck and postradiation angiosarcomas of the breast, local recurrence seems to have a crucial impact on OS. Therefore, improved local therapies and local tumor staging may have to be implemented. However, in deep soft tissue angiosarcomas, distant recurrence seems to have a major influence on prognosis, which indicates a benefit of additional perioperative chemotherapy. Hindawi 2021-09-10 /pmc/articles/PMC8449723/ /pubmed/34545273 http://dx.doi.org/10.1155/2021/9960085 Text en Copyright © 2021 Inna Schott et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Schott, Inna Liffers, Sven-Thorsten Farzaliyev, Farhad Falkenhorst, Johanna Steinau, Hans-Ulrich Treckmann, Jürgen-Walter Podleska, Lars Erik Pöttgen, Christoph Schildhaus, Hans-Ulrich Ahrens, Marit Dirksen, Uta Murat, Fatma-Zehra Siveke, Jens T. Bauer, Sebastian Hamacher, Rainer Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology |
title | Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology |
title_full | Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology |
title_fullStr | Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology |
title_full_unstemmed | Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology |
title_short | Localized Angiosarcoma, Not One Disease: A Retrospective Single-Center Study on Prognosis Depending on the Primary Site and Etiology |
title_sort | localized angiosarcoma, not one disease: a retrospective single-center study on prognosis depending on the primary site and etiology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449723/ https://www.ncbi.nlm.nih.gov/pubmed/34545273 http://dx.doi.org/10.1155/2021/9960085 |
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