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Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum

BACKGROUND: There is no standard treatment for giant cell tumors of the sacrum. We compared the outcomes and complications in patients with sacral giant cell tumors who underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies versus those who underwent non-surgical tre...

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Autores principales: Tsukamoto, Shinji, Ali, Nikolin, Mavrogenis, Andreas F., Honoki, Kanya, Tanaka, Yasuhito, Spinnato, Paolo, Donati, Davide Maria, Errani, Costantino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650241/
https://www.ncbi.nlm.nih.gov/pubmed/34872538
http://dx.doi.org/10.1186/s12891-021-04907-0
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author Tsukamoto, Shinji
Ali, Nikolin
Mavrogenis, Andreas F.
Honoki, Kanya
Tanaka, Yasuhito
Spinnato, Paolo
Donati, Davide Maria
Errani, Costantino
author_facet Tsukamoto, Shinji
Ali, Nikolin
Mavrogenis, Andreas F.
Honoki, Kanya
Tanaka, Yasuhito
Spinnato, Paolo
Donati, Davide Maria
Errani, Costantino
author_sort Tsukamoto, Shinji
collection PubMed
description BACKGROUND: There is no standard treatment for giant cell tumors of the sacrum. We compared the outcomes and complications in patients with sacral giant cell tumors who underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies versus those who underwent non-surgical treatment (denosumab therapy and/or embolization). METHODS: We retrospectively investigated 15 cases of sacral giant cell tumors treated at two institutions between 2005 and 2020. Nine patients underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies, and six patients received non-surgical treatment. The mean follow-up period was 85 months for the surgical group (range, 25–154 months) and 59 months (range, 17–94 months) for the non-surgical group. RESULTS: The local recurrence rate was 44% in the surgical group, and the tumor progression rate was 0% in the non-surgical group. There were two surgery-related complications (infection and bladder laceration) and three denosumab-related complications (apical granuloma of the tooth, stress fracture of the sacroiliac joint, and osteonecrosis of the jaw). In the surgical group, the mean modified Biagini score (bowel, bladder, and motor function) was 0.9; in the non-surgical group, it was 0.5. None of the 11 female patients became pregnant or delivered a baby after developing a sacral giant cell tumor. CONCLUSIONS: The cure rate of intralesional nerve-sparing surgery is over 50%. Non-surgical treatment has a similar risk of complications to intralesional nerve-sparing surgery and has better functional outcomes than intralesional nerve-sparing surgery, but patients must remain on therapy over time. Based on our results, the decision on the choice of treatment for sacral giant cell tumors could be discussed between the surgeon and the patient based on the tumor size and location.
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spelling pubmed-86502412021-12-07 Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum Tsukamoto, Shinji Ali, Nikolin Mavrogenis, Andreas F. Honoki, Kanya Tanaka, Yasuhito Spinnato, Paolo Donati, Davide Maria Errani, Costantino BMC Musculoskelet Disord Research BACKGROUND: There is no standard treatment for giant cell tumors of the sacrum. We compared the outcomes and complications in patients with sacral giant cell tumors who underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies versus those who underwent non-surgical treatment (denosumab therapy and/or embolization). METHODS: We retrospectively investigated 15 cases of sacral giant cell tumors treated at two institutions between 2005 and 2020. Nine patients underwent intralesional nerve-sparing surgery with or without (neo-) adjuvant therapies, and six patients received non-surgical treatment. The mean follow-up period was 85 months for the surgical group (range, 25–154 months) and 59 months (range, 17–94 months) for the non-surgical group. RESULTS: The local recurrence rate was 44% in the surgical group, and the tumor progression rate was 0% in the non-surgical group. There were two surgery-related complications (infection and bladder laceration) and three denosumab-related complications (apical granuloma of the tooth, stress fracture of the sacroiliac joint, and osteonecrosis of the jaw). In the surgical group, the mean modified Biagini score (bowel, bladder, and motor function) was 0.9; in the non-surgical group, it was 0.5. None of the 11 female patients became pregnant or delivered a baby after developing a sacral giant cell tumor. CONCLUSIONS: The cure rate of intralesional nerve-sparing surgery is over 50%. Non-surgical treatment has a similar risk of complications to intralesional nerve-sparing surgery and has better functional outcomes than intralesional nerve-sparing surgery, but patients must remain on therapy over time. Based on our results, the decision on the choice of treatment for sacral giant cell tumors could be discussed between the surgeon and the patient based on the tumor size and location. BioMed Central 2021-12-06 /pmc/articles/PMC8650241/ /pubmed/34872538 http://dx.doi.org/10.1186/s12891-021-04907-0 Text en © The Author(s) 2021 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
Tsukamoto, Shinji
Ali, Nikolin
Mavrogenis, Andreas F.
Honoki, Kanya
Tanaka, Yasuhito
Spinnato, Paolo
Donati, Davide Maria
Errani, Costantino
Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
title Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
title_full Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
title_fullStr Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
title_full_unstemmed Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
title_short Intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
title_sort intralesional nerve-sparing surgery versus non-surgical treatment for giant cell tumor of the sacrum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650241/
https://www.ncbi.nlm.nih.gov/pubmed/34872538
http://dx.doi.org/10.1186/s12891-021-04907-0
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