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The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature
OBJECTIVES: Retroperitoneal sarcomas (RPSs) are rare mesenchymal tumors. The objective of this study was to discuss the different clinical, therapeutic and prognostic aspects of RPS in our institution. METHODS: This was a retrospective study conducted at the Department of Medical Oncology in the Hab...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taibah University
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643528/ https://www.ncbi.nlm.nih.gov/pubmed/36398018 http://dx.doi.org/10.1016/j.jtumed.2022.07.007 |
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author | Feki, Jihene Lajnef, Maissa Fourati, Mohamed Sakka, Dhouha Hassena, Rania B. Slimen, Mourad H. Daoud, Jamel Khanfir, Afef |
author_facet | Feki, Jihene Lajnef, Maissa Fourati, Mohamed Sakka, Dhouha Hassena, Rania B. Slimen, Mourad H. Daoud, Jamel Khanfir, Afef |
author_sort | Feki, Jihene |
collection | PubMed |
description | OBJECTIVES: Retroperitoneal sarcomas (RPSs) are rare mesenchymal tumors. The objective of this study was to discuss the different clinical, therapeutic and prognostic aspects of RPS in our institution. METHODS: This was a retrospective study conducted at the Department of Medical Oncology in the Habib Bourguiba University Hospital in Sfax, including 19 patients who were treated for RPSs between 1999 and 2016. RESULTS: The median age was 49 years (range: 18–83 years); 68.4% of the patients were female. The commonest symptom was abdominal pain (88%) and the median tumor size was 15 cm (range: 4–30 cm). Complete resection was achieved in only five cases (26.3%). The most common histological subtypes were liposarcoma (47.4%) and leiomyosarcoma (26.3%). Eight patients had a high-grade tumor (G2 = 2 or G3 = 6). Adjuvant radiotherapy was administered in 5 patients (26%). Seventeen patients were treated with chemotherapy; six received chemotherapy in an adjuvant treatment, three as a neoadjuvant treatment, and eight were treated during the palliative phase. Relapse was observed in 58% of cases. For all patients, the overall survival (OS) was 89.5% at 1 year and 40.3% at 5 years. Prognostic factors influencing OS were sex (p = 0.037), resection margins (p = 0.02), recurrence (p = 0.042), and radiotherapy (p = 0.023). In multivariate analysis, radiotherapy (p = 0.031) and histological subtype (p = 0.028) were independent factors influencing OS and disease-free survival (DFS) respectively. CONCLUSION: We showed that the treatment of RPSs relies on surgery with complete resection. Other factors, such as radiotherapy and the occurrence of relapse, also have an impact on OS. To facilitate surgery and to obtain negative resection margins, preoperative radiotherapy is indicated in selected patients with a high risk of relapse. Further prospective trials are warranted to select optimal therapies with less toxicity and better efficacy in reducing recurrences, mainly at a local level. |
format | Online Article Text |
id | pubmed-9643528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taibah University |
record_format | MEDLINE/PubMed |
spelling | pubmed-96435282022-11-16 The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature Feki, Jihene Lajnef, Maissa Fourati, Mohamed Sakka, Dhouha Hassena, Rania B. Slimen, Mourad H. Daoud, Jamel Khanfir, Afef J Taibah Univ Med Sci Original Article OBJECTIVES: Retroperitoneal sarcomas (RPSs) are rare mesenchymal tumors. The objective of this study was to discuss the different clinical, therapeutic and prognostic aspects of RPS in our institution. METHODS: This was a retrospective study conducted at the Department of Medical Oncology in the Habib Bourguiba University Hospital in Sfax, including 19 patients who were treated for RPSs between 1999 and 2016. RESULTS: The median age was 49 years (range: 18–83 years); 68.4% of the patients were female. The commonest symptom was abdominal pain (88%) and the median tumor size was 15 cm (range: 4–30 cm). Complete resection was achieved in only five cases (26.3%). The most common histological subtypes were liposarcoma (47.4%) and leiomyosarcoma (26.3%). Eight patients had a high-grade tumor (G2 = 2 or G3 = 6). Adjuvant radiotherapy was administered in 5 patients (26%). Seventeen patients were treated with chemotherapy; six received chemotherapy in an adjuvant treatment, three as a neoadjuvant treatment, and eight were treated during the palliative phase. Relapse was observed in 58% of cases. For all patients, the overall survival (OS) was 89.5% at 1 year and 40.3% at 5 years. Prognostic factors influencing OS were sex (p = 0.037), resection margins (p = 0.02), recurrence (p = 0.042), and radiotherapy (p = 0.023). In multivariate analysis, radiotherapy (p = 0.031) and histological subtype (p = 0.028) were independent factors influencing OS and disease-free survival (DFS) respectively. CONCLUSION: We showed that the treatment of RPSs relies on surgery with complete resection. Other factors, such as radiotherapy and the occurrence of relapse, also have an impact on OS. To facilitate surgery and to obtain negative resection margins, preoperative radiotherapy is indicated in selected patients with a high risk of relapse. Further prospective trials are warranted to select optimal therapies with less toxicity and better efficacy in reducing recurrences, mainly at a local level. Taibah University 2022-08-18 /pmc/articles/PMC9643528/ /pubmed/36398018 http://dx.doi.org/10.1016/j.jtumed.2022.07.007 Text en © 2022 [The Author/The Authors] https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Feki, Jihene Lajnef, Maissa Fourati, Mohamed Sakka, Dhouha Hassena, Rania B. Slimen, Mourad H. Daoud, Jamel Khanfir, Afef The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature |
title | The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature |
title_full | The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature |
title_fullStr | The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature |
title_full_unstemmed | The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature |
title_short | The management of retroperitoneal sarcoma: The experience of a single institution and a review of the literature |
title_sort | management of retroperitoneal sarcoma: the experience of a single institution and a review of the literature |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643528/ https://www.ncbi.nlm.nih.gov/pubmed/36398018 http://dx.doi.org/10.1016/j.jtumed.2022.07.007 |
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