Loading…
Uterine leiomyosarcoma: A review of the literature and update on management options
Uterine leiomyosarcoma is the most common type of uterine sarcoma. It is an extremely aggressive malignancy associated with a poor overall prognosis. Women affected may vary in age, but are most often diagnosed in their perimenopausal years. Presenting symptoms may be vague and mimic other benign ut...
Saved in:
Published in: | Gynecologic oncology 2018-12, Vol.151 (3), p.562-572 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3 |
container_end_page | 572 |
container_issue | 3 |
container_start_page | 562 |
container_title | Gynecologic oncology |
container_volume | 151 |
creator | Roberts, Maureen E. Aynardi, Jason T. Chu, Christina S. |
description | Uterine leiomyosarcoma is the most common type of uterine sarcoma. It is an extremely aggressive malignancy associated with a poor overall prognosis. Women affected may vary in age, but are most often diagnosed in their perimenopausal years. Presenting symptoms may be vague and mimic other benign uterine conditions. Preoperative diagnosis of leiomyosarcoma is difficult and often only made at time of surgical resection. These rare mesenchymal tumors are characterized by cytologic atypia, a high mitotic index, and tumor necrosis on histologic inspection. Management of early stage disease entails hysterectomy and complete surgical resection of gross tumor, though routine oophorectomy or lymph node dissection do not appear to confer much clinical benefit. Adjuvant therapy for early stage disease remains controversial as multiple clinical trials have failed to demonstrate benefit on overall survival. Recently, progress has been made in regards to therapy for advanced and recurrent disease. Novel chemotherapeutics, targeted therapies such as olaratumab and pazopanib, and new immunotherapies such as nivolumab and pembrolizumab have demonstrated promise in these previously difficult drug-resistant patients. In this article, we provide a detailed review of uterine leiomyosarcoma including epidemiology, clinical presentation, diagnosis, and pathologic characteristics. We then go on detail management strategies, including options for adjuvant therapy, and highlight new and developing regimens in the field.
•Uterine morcellation should be discouraged due to the risk of intraperitoneal dissemination of malignant tissue.•Adjuvant therapy for uterine-confined disease remains controversial as no improvement in survival has been demonstrated.•Adding olaratumab to doxorubicin for the treatment of advanced disease improves survival compared to doxorubicin alone. |
doi_str_mv | 10.1016/j.ygyno.2018.09.010 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2111744524</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0090825818312216</els_id><sourcerecordid>2111744524</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3</originalsourceid><addsrcrecordid>eNp9kE1P3DAQhi1UBMuWX1Cp8rGXpOOvJEbqASFoKyH1QDlbjjMBrzb2Yjug_feELu2xpznM876jeQj5xKBmwJqvm3r_sA-x5sC6GnQNDI7IioFWVdMp_YGsADRUHVfdKTnLeQMAAhg_IacCuJS6gRW5uy-YfEC6RR-nfcw2uTjZC3pJEz57fKFxpOVx2fsFtGVOSG0Y6LwbbEEaA51ssA84YSg07oqPIX8kx6PdZjx_n2tyf3P9--pHdfvr-8-ry9vKyVaVyvaKaQ7Yt1wKKYXiVjqnW65V3w-tgmbkfTug4qIB3YEcFIpOC87GVo-dFWvy5dC7S_FpxlzM5LPD7dYGjHM2nDHWSqmW-jURB9SlmHPC0eySn2zaGwbmzabZmD82zZtNA9osNpfU5_cDcz_h8C_zV98CfDsAuLy52EomO4_B4eATumKG6P974BXcXYan</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2111744524</pqid></control><display><type>article</type><title>Uterine leiomyosarcoma: A review of the literature and update on management options</title><source>ScienceDirect Freedom Collection</source><creator>Roberts, Maureen E. ; Aynardi, Jason T. ; Chu, Christina S.</creator><creatorcontrib>Roberts, Maureen E. ; Aynardi, Jason T. ; Chu, Christina S.</creatorcontrib><description>Uterine leiomyosarcoma is the most common type of uterine sarcoma. It is an extremely aggressive malignancy associated with a poor overall prognosis. Women affected may vary in age, but are most often diagnosed in their perimenopausal years. Presenting symptoms may be vague and mimic other benign uterine conditions. Preoperative diagnosis of leiomyosarcoma is difficult and often only made at time of surgical resection. These rare mesenchymal tumors are characterized by cytologic atypia, a high mitotic index, and tumor necrosis on histologic inspection. Management of early stage disease entails hysterectomy and complete surgical resection of gross tumor, though routine oophorectomy or lymph node dissection do not appear to confer much clinical benefit. Adjuvant therapy for early stage disease remains controversial as multiple clinical trials have failed to demonstrate benefit on overall survival. Recently, progress has been made in regards to therapy for advanced and recurrent disease. Novel chemotherapeutics, targeted therapies such as olaratumab and pazopanib, and new immunotherapies such as nivolumab and pembrolizumab have demonstrated promise in these previously difficult drug-resistant patients. In this article, we provide a detailed review of uterine leiomyosarcoma including epidemiology, clinical presentation, diagnosis, and pathologic characteristics. We then go on detail management strategies, including options for adjuvant therapy, and highlight new and developing regimens in the field.
•Uterine morcellation should be discouraged due to the risk of intraperitoneal dissemination of malignant tissue.•Adjuvant therapy for uterine-confined disease remains controversial as no improvement in survival has been demonstrated.•Adding olaratumab to doxorubicin for the treatment of advanced disease improves survival compared to doxorubicin alone.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2018.09.010</identifier><identifier>PMID: 30244960</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Chemothearpy ; Female ; Humans ; Leiomyosarcoma ; Leiomyosarcoma - diagnosis ; Leiomyosarcoma - pathology ; Leiomyosarcoma - therapy ; Morcellation ; Radiation ; Targeted therapy ; Uterine Neoplasms - diagnosis ; Uterine Neoplasms - pathology ; Uterine Neoplasms - therapy ; Uterine sarcoma</subject><ispartof>Gynecologic oncology, 2018-12, Vol.151 (3), p.562-572</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3</citedby><cites>FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30244960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roberts, Maureen E.</creatorcontrib><creatorcontrib>Aynardi, Jason T.</creatorcontrib><creatorcontrib>Chu, Christina S.</creatorcontrib><title>Uterine leiomyosarcoma: A review of the literature and update on management options</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Uterine leiomyosarcoma is the most common type of uterine sarcoma. It is an extremely aggressive malignancy associated with a poor overall prognosis. Women affected may vary in age, but are most often diagnosed in their perimenopausal years. Presenting symptoms may be vague and mimic other benign uterine conditions. Preoperative diagnosis of leiomyosarcoma is difficult and often only made at time of surgical resection. These rare mesenchymal tumors are characterized by cytologic atypia, a high mitotic index, and tumor necrosis on histologic inspection. Management of early stage disease entails hysterectomy and complete surgical resection of gross tumor, though routine oophorectomy or lymph node dissection do not appear to confer much clinical benefit. Adjuvant therapy for early stage disease remains controversial as multiple clinical trials have failed to demonstrate benefit on overall survival. Recently, progress has been made in regards to therapy for advanced and recurrent disease. Novel chemotherapeutics, targeted therapies such as olaratumab and pazopanib, and new immunotherapies such as nivolumab and pembrolizumab have demonstrated promise in these previously difficult drug-resistant patients. In this article, we provide a detailed review of uterine leiomyosarcoma including epidemiology, clinical presentation, diagnosis, and pathologic characteristics. We then go on detail management strategies, including options for adjuvant therapy, and highlight new and developing regimens in the field.
•Uterine morcellation should be discouraged due to the risk of intraperitoneal dissemination of malignant tissue.•Adjuvant therapy for uterine-confined disease remains controversial as no improvement in survival has been demonstrated.•Adding olaratumab to doxorubicin for the treatment of advanced disease improves survival compared to doxorubicin alone.</description><subject>Chemothearpy</subject><subject>Female</subject><subject>Humans</subject><subject>Leiomyosarcoma</subject><subject>Leiomyosarcoma - diagnosis</subject><subject>Leiomyosarcoma - pathology</subject><subject>Leiomyosarcoma - therapy</subject><subject>Morcellation</subject><subject>Radiation</subject><subject>Targeted therapy</subject><subject>Uterine Neoplasms - diagnosis</subject><subject>Uterine Neoplasms - pathology</subject><subject>Uterine Neoplasms - therapy</subject><subject>Uterine sarcoma</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhi1UBMuWX1Cp8rGXpOOvJEbqASFoKyH1QDlbjjMBrzb2Yjug_feELu2xpznM876jeQj5xKBmwJqvm3r_sA-x5sC6GnQNDI7IioFWVdMp_YGsADRUHVfdKTnLeQMAAhg_IacCuJS6gRW5uy-YfEC6RR-nfcw2uTjZC3pJEz57fKFxpOVx2fsFtGVOSG0Y6LwbbEEaA51ssA84YSg07oqPIX8kx6PdZjx_n2tyf3P9--pHdfvr-8-ry9vKyVaVyvaKaQ7Yt1wKKYXiVjqnW65V3w-tgmbkfTug4qIB3YEcFIpOC87GVo-dFWvy5dC7S_FpxlzM5LPD7dYGjHM2nDHWSqmW-jURB9SlmHPC0eySn2zaGwbmzabZmD82zZtNA9osNpfU5_cDcz_h8C_zV98CfDsAuLy52EomO4_B4eATumKG6P974BXcXYan</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Roberts, Maureen E.</creator><creator>Aynardi, Jason T.</creator><creator>Chu, Christina S.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201812</creationdate><title>Uterine leiomyosarcoma: A review of the literature and update on management options</title><author>Roberts, Maureen E. ; Aynardi, Jason T. ; Chu, Christina S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Chemothearpy</topic><topic>Female</topic><topic>Humans</topic><topic>Leiomyosarcoma</topic><topic>Leiomyosarcoma - diagnosis</topic><topic>Leiomyosarcoma - pathology</topic><topic>Leiomyosarcoma - therapy</topic><topic>Morcellation</topic><topic>Radiation</topic><topic>Targeted therapy</topic><topic>Uterine Neoplasms - diagnosis</topic><topic>Uterine Neoplasms - pathology</topic><topic>Uterine Neoplasms - therapy</topic><topic>Uterine sarcoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roberts, Maureen E.</creatorcontrib><creatorcontrib>Aynardi, Jason T.</creatorcontrib><creatorcontrib>Chu, Christina S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gynecologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roberts, Maureen E.</au><au>Aynardi, Jason T.</au><au>Chu, Christina S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Uterine leiomyosarcoma: A review of the literature and update on management options</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2018-12</date><risdate>2018</risdate><volume>151</volume><issue>3</issue><spage>562</spage><epage>572</epage><pages>562-572</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>Uterine leiomyosarcoma is the most common type of uterine sarcoma. It is an extremely aggressive malignancy associated with a poor overall prognosis. Women affected may vary in age, but are most often diagnosed in their perimenopausal years. Presenting symptoms may be vague and mimic other benign uterine conditions. Preoperative diagnosis of leiomyosarcoma is difficult and often only made at time of surgical resection. These rare mesenchymal tumors are characterized by cytologic atypia, a high mitotic index, and tumor necrosis on histologic inspection. Management of early stage disease entails hysterectomy and complete surgical resection of gross tumor, though routine oophorectomy or lymph node dissection do not appear to confer much clinical benefit. Adjuvant therapy for early stage disease remains controversial as multiple clinical trials have failed to demonstrate benefit on overall survival. Recently, progress has been made in regards to therapy for advanced and recurrent disease. Novel chemotherapeutics, targeted therapies such as olaratumab and pazopanib, and new immunotherapies such as nivolumab and pembrolizumab have demonstrated promise in these previously difficult drug-resistant patients. In this article, we provide a detailed review of uterine leiomyosarcoma including epidemiology, clinical presentation, diagnosis, and pathologic characteristics. We then go on detail management strategies, including options for adjuvant therapy, and highlight new and developing regimens in the field.
•Uterine morcellation should be discouraged due to the risk of intraperitoneal dissemination of malignant tissue.•Adjuvant therapy for uterine-confined disease remains controversial as no improvement in survival has been demonstrated.•Adding olaratumab to doxorubicin for the treatment of advanced disease improves survival compared to doxorubicin alone.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30244960</pmid><doi>10.1016/j.ygyno.2018.09.010</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0090-8258 |
ispartof | Gynecologic oncology, 2018-12, Vol.151 (3), p.562-572 |
issn | 0090-8258 1095-6859 |
language | eng |
recordid | cdi_proquest_miscellaneous_2111744524 |
source | ScienceDirect Freedom Collection |
subjects | Chemothearpy Female Humans Leiomyosarcoma Leiomyosarcoma - diagnosis Leiomyosarcoma - pathology Leiomyosarcoma - therapy Morcellation Radiation Targeted therapy Uterine Neoplasms - diagnosis Uterine Neoplasms - pathology Uterine Neoplasms - therapy Uterine sarcoma |
title | Uterine leiomyosarcoma: A review of the literature and update on management options |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T16%3A22%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Uterine%20leiomyosarcoma:%20A%20review%20of%20the%20literature%20and%20update%20on%20management%20options&rft.jtitle=Gynecologic%20oncology&rft.au=Roberts,%20Maureen%20E.&rft.date=2018-12&rft.volume=151&rft.issue=3&rft.spage=562&rft.epage=572&rft.pages=562-572&rft.issn=0090-8258&rft.eissn=1095-6859&rft_id=info:doi/10.1016/j.ygyno.2018.09.010&rft_dat=%3Cproquest_cross%3E2111744524%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-ab51920eb724344352a4cc97295bbd7506f2b7de523609804d5e389321f79f8a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2111744524&rft_id=info:pmid/30244960&rfr_iscdi=true |