Prognostic Features of Sarcomas and Mixed Tumors of the Endometrium

A retrospective study of 103 patients with endometrial sarcomas treated at the University of Michigan Hospital includes 47 mixed homologous tumors, 32 mixed heterologous tumors, 21 pure homologous sarcomas (endometrial stromal sarcoma), and three pure heterologous sarcomas (rhabdomyosarcomas). Clini...

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Veröffentlicht in:Obstetrics and gynecology (New York. 1953) 1984-04, Vol.63 (4), p.550-556
Hauptverfasser: PETERS, WILLIAM A, KUMAR, NEELAM B, FLEMING, WILLIAM P, MORLEY, GEORGE W
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container_title Obstetrics and gynecology (New York. 1953)
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creator PETERS, WILLIAM A
KUMAR, NEELAM B
FLEMING, WILLIAM P
MORLEY, GEORGE W
description A retrospective study of 103 patients with endometrial sarcomas treated at the University of Michigan Hospital includes 47 mixed homologous tumors, 32 mixed heterologous tumors, 21 pure homologous sarcomas (endometrial stromal sarcoma), and three pure heterologous sarcomas (rhabdomyosarcomas). Clinical characteristics appeared similar among the four patient groups. Fourteen percent of the patients had received previous pelvic irradiation. Twenty- nine percent of the patients with a clinical stage I or II tumor had extrauterine disease discovered at surgery. Extent of the tumor at the time of surgery strongly correlated with outcome, and only two patients with extrauterine disease were long-term survivors. Life table survival probability at five years was 58% with surgical stage 1, 33% with surgical stage 2, 13% with surgical stage 3, 0 with surgical stage 5, and 5% in patients referred with recurrence. Risk factors predicting treatment failure were analyzed separately in surgical stages I and II using Cox model analysis. There was no difference in risk for treatment failure between pure endometrial stromal sarcoma, mixed homologous sarcoma, or mixed heterologous sarcoma. The strongest factor correlating with a poor outcome was deep myometrial invasion (P < .001). An adverse trend was detected in those patients with previous pelvic irradiation, with advancing patient age, and with increasing uterine size, although these differences did not reach statistical significance. Neither the presence of heterologous tumor elements nor cervical involvement were found to be adverse prognostic factors.
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Clinical characteristics appeared similar among the four patient groups. Fourteen percent of the patients had received previous pelvic irradiation. Twenty- nine percent of the patients with a clinical stage I or II tumor had extrauterine disease discovered at surgery. Extent of the tumor at the time of surgery strongly correlated with outcome, and only two patients with extrauterine disease were long-term survivors. Life table survival probability at five years was 58% with surgical stage 1, 33% with surgical stage 2, 13% with surgical stage 3, 0 with surgical stage 5, and 5% in patients referred with recurrence. Risk factors predicting treatment failure were analyzed separately in surgical stages I and II using Cox model analysis. There was no difference in risk for treatment failure between pure endometrial stromal sarcoma, mixed homologous sarcoma, or mixed heterologous sarcoma. The strongest factor correlating with a poor outcome was deep myometrial invasion (P &lt; .001). An adverse trend was detected in those patients with previous pelvic irradiation, with advancing patient age, and with increasing uterine size, although these differences did not reach statistical significance. Neither the presence of heterologous tumor elements nor cervical involvement were found to be adverse prognostic factors.</description><identifier>ISSN: 0029-7844</identifier><identifier>EISSN: 1873-233X</identifier><identifier>PMID: 6322081</identifier><identifier>CODEN: OBGNAS</identifier><language>eng</language><publisher>New York, NY: The American College of Obstetricians and Gynecologists</publisher><subject>Actuarial Analysis ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adenocarcinoma - therapy ; Biological and medical sciences ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - therapy ; Combined Modality Therapy ; Female ; Female genital diseases ; Gynecology. Andrology. Obstetrics ; Humans ; Hysterectomy ; Medical sciences ; Middle Aged ; Neoplasms, Germ Cell and Embryonal - mortality ; Neoplasms, Germ Cell and Embryonal - pathology ; Neoplasms, Germ Cell and Embryonal - therapy ; Prognosis ; Retrospective Studies ; Rhabdomyosarcoma - mortality ; Rhabdomyosarcoma - pathology ; Rhabdomyosarcoma - therapy ; Sarcoma - mortality ; Sarcoma - pathology ; Sarcoma - therapy ; Tumors ; Uterine Neoplasms - mortality ; Uterine Neoplasms - pathology ; Uterine Neoplasms - therapy</subject><ispartof>Obstetrics and gynecology (New York. 1953), 1984-04, Vol.63 (4), p.550-556</ispartof><rights>1984 The American College of Obstetricians and Gynecologists</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=9233413$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6322081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PETERS, WILLIAM A</creatorcontrib><creatorcontrib>KUMAR, NEELAM B</creatorcontrib><creatorcontrib>FLEMING, WILLIAM P</creatorcontrib><creatorcontrib>MORLEY, GEORGE W</creatorcontrib><title>Prognostic Features of Sarcomas and Mixed Tumors of the Endometrium</title><title>Obstetrics and gynecology (New York. 1953)</title><addtitle>Obstet Gynecol</addtitle><description>A retrospective study of 103 patients with endometrial sarcomas treated at the University of Michigan Hospital includes 47 mixed homologous tumors, 32 mixed heterologous tumors, 21 pure homologous sarcomas (endometrial stromal sarcoma), and three pure heterologous sarcomas (rhabdomyosarcomas). Clinical characteristics appeared similar among the four patient groups. Fourteen percent of the patients had received previous pelvic irradiation. Twenty- nine percent of the patients with a clinical stage I or II tumor had extrauterine disease discovered at surgery. Extent of the tumor at the time of surgery strongly correlated with outcome, and only two patients with extrauterine disease were long-term survivors. Life table survival probability at five years was 58% with surgical stage 1, 33% with surgical stage 2, 13% with surgical stage 3, 0 with surgical stage 5, and 5% in patients referred with recurrence. Risk factors predicting treatment failure were analyzed separately in surgical stages I and II using Cox model analysis. There was no difference in risk for treatment failure between pure endometrial stromal sarcoma, mixed homologous sarcoma, or mixed heterologous sarcoma. The strongest factor correlating with a poor outcome was deep myometrial invasion (P &lt; .001). An adverse trend was detected in those patients with previous pelvic irradiation, with advancing patient age, and with increasing uterine size, although these differences did not reach statistical significance. Neither the presence of heterologous tumor elements nor cervical involvement were found to be adverse prognostic factors.</description><subject>Actuarial Analysis</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - therapy</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Hysterectomy</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasms, Germ Cell and Embryonal - mortality</subject><subject>Neoplasms, Germ Cell and Embryonal - pathology</subject><subject>Neoplasms, Germ Cell and Embryonal - therapy</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Rhabdomyosarcoma - mortality</subject><subject>Rhabdomyosarcoma - pathology</subject><subject>Rhabdomyosarcoma - therapy</subject><subject>Sarcoma - mortality</subject><subject>Sarcoma - pathology</subject><subject>Sarcoma - therapy</subject><subject>Tumors</subject><subject>Uterine Neoplasms - mortality</subject><subject>Uterine Neoplasms - pathology</subject><subject>Uterine Neoplasms - therapy</subject><issn>0029-7844</issn><issn>1873-233X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1LxDAQhoso67r6E4QexFth8tE0OcqyfsCKgit4K9MkdattsyYtq__e4BYPw8vwPAzMe5TMiSxYRhl7O07mAFRlheT8NDkL4QMAiFBslswEoxQkmSfLZ-_eexeGRqe3FofR25C6On1Br12HIcXepI_NtzXpZuyc_4PD1qar3rjODr4Zu_PkpMY22IspF8nr7WqzvM_WT3cPy5t1tqMSaKaxEJUABFkYURteE45Q11rIXHFtOKjc8twAajRcEkspSopCEyqUElXFFsn14e7Ou6_RhqHsmqBt22Jv3RhKCdEDCVG8nMSx6qwpd77p0P-U09eRX00cg8a29tjrJvxrKrbHCYsaP2h71w7Wh8923Ftfbi22w7aMZYKgOWRESQ48blkcStkvk-BwEg</recordid><startdate>198404</startdate><enddate>198404</enddate><creator>PETERS, WILLIAM A</creator><creator>KUMAR, NEELAM B</creator><creator>FLEMING, WILLIAM P</creator><creator>MORLEY, GEORGE W</creator><general>The American College of Obstetricians and Gynecologists</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>198404</creationdate><title>Prognostic Features of Sarcomas and Mixed Tumors of the Endometrium</title><author>PETERS, WILLIAM A ; KUMAR, NEELAM B ; FLEMING, WILLIAM P ; MORLEY, GEORGE W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2802-ca76b60a087d6fd4f14a0ffc68594cd4095e45d0acad481e22a82a6c126996bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Actuarial Analysis</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - therapy</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Hysterectomy</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasms, Germ Cell and Embryonal - mortality</topic><topic>Neoplasms, Germ Cell and Embryonal - pathology</topic><topic>Neoplasms, Germ Cell and Embryonal - therapy</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Rhabdomyosarcoma - mortality</topic><topic>Rhabdomyosarcoma - pathology</topic><topic>Rhabdomyosarcoma - therapy</topic><topic>Sarcoma - mortality</topic><topic>Sarcoma - pathology</topic><topic>Sarcoma - therapy</topic><topic>Tumors</topic><topic>Uterine Neoplasms - mortality</topic><topic>Uterine Neoplasms - pathology</topic><topic>Uterine Neoplasms - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PETERS, WILLIAM A</creatorcontrib><creatorcontrib>KUMAR, NEELAM B</creatorcontrib><creatorcontrib>FLEMING, WILLIAM P</creatorcontrib><creatorcontrib>MORLEY, GEORGE W</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Obstetrics and gynecology (New York. 1953)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PETERS, WILLIAM A</au><au>KUMAR, NEELAM B</au><au>FLEMING, WILLIAM P</au><au>MORLEY, GEORGE W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic Features of Sarcomas and Mixed Tumors of the Endometrium</atitle><jtitle>Obstetrics and gynecology (New York. 1953)</jtitle><addtitle>Obstet Gynecol</addtitle><date>1984-04</date><risdate>1984</risdate><volume>63</volume><issue>4</issue><spage>550</spage><epage>556</epage><pages>550-556</pages><issn>0029-7844</issn><eissn>1873-233X</eissn><coden>OBGNAS</coden><abstract>A retrospective study of 103 patients with endometrial sarcomas treated at the University of Michigan Hospital includes 47 mixed homologous tumors, 32 mixed heterologous tumors, 21 pure homologous sarcomas (endometrial stromal sarcoma), and three pure heterologous sarcomas (rhabdomyosarcomas). Clinical characteristics appeared similar among the four patient groups. Fourteen percent of the patients had received previous pelvic irradiation. Twenty- nine percent of the patients with a clinical stage I or II tumor had extrauterine disease discovered at surgery. Extent of the tumor at the time of surgery strongly correlated with outcome, and only two patients with extrauterine disease were long-term survivors. Life table survival probability at five years was 58% with surgical stage 1, 33% with surgical stage 2, 13% with surgical stage 3, 0 with surgical stage 5, and 5% in patients referred with recurrence. Risk factors predicting treatment failure were analyzed separately in surgical stages I and II using Cox model analysis. There was no difference in risk for treatment failure between pure endometrial stromal sarcoma, mixed homologous sarcoma, or mixed heterologous sarcoma. The strongest factor correlating with a poor outcome was deep myometrial invasion (P &lt; .001). An adverse trend was detected in those patients with previous pelvic irradiation, with advancing patient age, and with increasing uterine size, although these differences did not reach statistical significance. Neither the presence of heterologous tumor elements nor cervical involvement were found to be adverse prognostic factors.</abstract><cop>New York, NY</cop><pub>The American College of Obstetricians and Gynecologists</pub><pmid>6322081</pmid><tpages>7</tpages></addata></record>
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source MEDLINE; Journals@Ovid Complete
subjects Actuarial Analysis
Adenocarcinoma - mortality
Adenocarcinoma - pathology
Adenocarcinoma - therapy
Biological and medical sciences
Carcinoma, Squamous Cell - mortality
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - therapy
Combined Modality Therapy
Female
Female genital diseases
Gynecology. Andrology. Obstetrics
Humans
Hysterectomy
Medical sciences
Middle Aged
Neoplasms, Germ Cell and Embryonal - mortality
Neoplasms, Germ Cell and Embryonal - pathology
Neoplasms, Germ Cell and Embryonal - therapy
Prognosis
Retrospective Studies
Rhabdomyosarcoma - mortality
Rhabdomyosarcoma - pathology
Rhabdomyosarcoma - therapy
Sarcoma - mortality
Sarcoma - pathology
Sarcoma - therapy
Tumors
Uterine Neoplasms - mortality
Uterine Neoplasms - pathology
Uterine Neoplasms - therapy
title Prognostic Features of Sarcomas and Mixed Tumors of the Endometrium
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