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Uterine Leiomyosarcoma

Leiomyosarcoma (LMS) is the most common soft tissue sarcoma in adults and can occur in any part of the body. Uterine leiomyosarcoma (uLMS) is the most common location for LMS, making up 2% to 5% of all uterine malignancies. It is an aggressive tumor that is challenging to treat because of its resist...

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Autores principales: Byar, Katherine L., Fredericks, Tricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Harborside Press LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805803/
https://www.ncbi.nlm.nih.gov/pubmed/35173990
http://dx.doi.org/10.6004/jadpro.2022.13.1.6
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author Byar, Katherine L.
Fredericks, Tricia
author_facet Byar, Katherine L.
Fredericks, Tricia
author_sort Byar, Katherine L.
collection PubMed
description Leiomyosarcoma (LMS) is the most common soft tissue sarcoma in adults and can occur in any part of the body. Uterine leiomyosarcoma (uLMS) is the most common location for LMS, making up 2% to 5% of all uterine malignancies. It is an aggressive tumor that is challenging to treat because of its resistance to standard therapy. The majority of patients (60%) are diagnosed with early-stage disease. However, regardless of the stage, uLMS has a poor prognosis. Surgical resection is the cornerstone of treatment for patients with localized LMS independent of the site of origin. Adjuvant chemotherapy for early-stage disease remains controversial as multiple clinical trials have failed to demonstrate benefit on overall survival. Progress has been made in therapy for advanced and recurrent disease. This case study will highlight the current and emerging data regarding novel therapies for women with uLMS.
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spelling pubmed-88058032022-02-15 Uterine Leiomyosarcoma Byar, Katherine L. Fredericks, Tricia J Adv Pract Oncol Grand Rounds Leiomyosarcoma (LMS) is the most common soft tissue sarcoma in adults and can occur in any part of the body. Uterine leiomyosarcoma (uLMS) is the most common location for LMS, making up 2% to 5% of all uterine malignancies. It is an aggressive tumor that is challenging to treat because of its resistance to standard therapy. The majority of patients (60%) are diagnosed with early-stage disease. However, regardless of the stage, uLMS has a poor prognosis. Surgical resection is the cornerstone of treatment for patients with localized LMS independent of the site of origin. Adjuvant chemotherapy for early-stage disease remains controversial as multiple clinical trials have failed to demonstrate benefit on overall survival. Progress has been made in therapy for advanced and recurrent disease. This case study will highlight the current and emerging data regarding novel therapies for women with uLMS. Harborside Press LLC 2022-01 2022-02-01 /pmc/articles/PMC8805803/ /pubmed/35173990 http://dx.doi.org/10.6004/jadpro.2022.13.1.6 Text en © 2022 Harborside™ https://creativecommons.org/licenses/by-nc-nd/3.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial Non-Derivative License, which permits unrestricted non-commercial and non-derivative use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Grand Rounds
Byar, Katherine L.
Fredericks, Tricia
Uterine Leiomyosarcoma
title Uterine Leiomyosarcoma
title_full Uterine Leiomyosarcoma
title_fullStr Uterine Leiomyosarcoma
title_full_unstemmed Uterine Leiomyosarcoma
title_short Uterine Leiomyosarcoma
title_sort uterine leiomyosarcoma
topic Grand Rounds
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805803/
https://www.ncbi.nlm.nih.gov/pubmed/35173990
http://dx.doi.org/10.6004/jadpro.2022.13.1.6
work_keys_str_mv AT byarkatherinel uterineleiomyosarcoma
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