Heterogeneity of stage IIIA endometrial carcinomas: implications for adjuvant therapy
The purpose of this study was to evaluate overall survival (OS) and determine prognostic subclassifications for stage IIIA endometrial cancer. Stage IIIA endometrial cancer patients treated at M.D. Anderson Cancer Center from 1989 to 2002 were reviewed. Clinical information was obtained from the med...
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Veröffentlicht in: | International journal of gynecological cancer 2005-04, Vol.15 (3), p.510-516 |
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creator | Slomovitz, B.M. Ramondetta, L.M. Lee, C.M. Oh, J.C. Eifel, P.J. Jhingran, A. Burke, T.W. Gershenson, D.M. Lu, K.H. |
description | The purpose of this study was to evaluate overall survival (OS) and determine prognostic subclassifications for stage IIIA endometrial cancer. Stage IIIA endometrial cancer patients treated at M.D. Anderson Cancer Center from 1989 to 2002 were reviewed. Clinical information was obtained from the medical record. Cox regression analyses were performed to evaluate the association of pathologic criteria and OS. Patients were divided into four groups based on this analysis: E1, endometrioid/pelvic cytology only; E2, endometrioid/adnexa ± serosal spread; NE1, nonendometrioid/pelvic cytology only; and NE2, nonendometrioid/adenexa ± serosal spread. Forty-nine patients were identified. By multivariate analysis, histology and extent of disease were the only factors associated with OS. Five-year OS in the four subgroups based on histology and extent of disease were: E1, 79%, E2, 65%, NE1, 64%, and NE2, 13%. Histologic subtype and extent of pelvic disease are the only prognostic factors associated with OS. Patients with endometrioid tumors and extent of pelvic disease limited to positive cytology had a favorable outcome, with or without adjuvant therapy. Future prospective clinical trials should consider subclassifying patients with stage IIIA disease to better evaluate the role of adjuvant therapy. |
doi_str_mv | 10.1136/ijgc-00009577-200505000-00016 |
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Stage IIIA endometrial cancer patients treated at M.D. Anderson Cancer Center from 1989 to 2002 were reviewed. Clinical information was obtained from the medical record. Cox regression analyses were performed to evaluate the association of pathologic criteria and OS. Patients were divided into four groups based on this analysis: E1, endometrioid/pelvic cytology only; E2, endometrioid/adnexa ± serosal spread; NE1, nonendometrioid/pelvic cytology only; and NE2, nonendometrioid/adenexa ± serosal spread. Forty-nine patients were identified. By multivariate analysis, histology and extent of disease were the only factors associated with OS. Five-year OS in the four subgroups based on histology and extent of disease were: E1, 79%, E2, 65%, NE1, 64%, and NE2, 13%. Histologic subtype and extent of pelvic disease are the only prognostic factors associated with OS. Patients with endometrioid tumors and extent of pelvic disease limited to positive cytology had a favorable outcome, with or without adjuvant therapy. Future prospective clinical trials should consider subclassifying patients with stage IIIA disease to better evaluate the role of adjuvant therapy.</description><identifier>ISSN: 1048-891X</identifier><identifier>EISSN: 1525-1438</identifier><identifier>DOI: 10.1136/ijgc-00009577-200505000-00016</identifier><language>eng</language><publisher>Kidlington: Elsevier Limited</publisher><subject>Cellular biology ; Endometrial cancer ; Histology ; Medical prognosis</subject><ispartof>International journal of gynecological cancer, 2005-04, Vol.15 (3), p.510-516</ispartof><rights>Copyright © 2005 Blackwell Publishing Ltd.2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2084-c5ce3e9adb97960a69b022fa208bd3cf069dca3d1481b31e5877ab8ded280c373</citedby><cites>FETCH-LOGICAL-c2084-c5ce3e9adb97960a69b022fa208bd3cf069dca3d1481b31e5877ab8ded280c373</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></links><search><creatorcontrib>Slomovitz, B.M.</creatorcontrib><creatorcontrib>Ramondetta, L.M.</creatorcontrib><creatorcontrib>Lee, C.M.</creatorcontrib><creatorcontrib>Oh, J.C.</creatorcontrib><creatorcontrib>Eifel, P.J.</creatorcontrib><creatorcontrib>Jhingran, A.</creatorcontrib><creatorcontrib>Burke, T.W.</creatorcontrib><creatorcontrib>Gershenson, D.M.</creatorcontrib><creatorcontrib>Lu, K.H.</creatorcontrib><title>Heterogeneity of stage IIIA endometrial carcinomas: implications for adjuvant therapy</title><title>International journal of gynecological cancer</title><description>The purpose of this study was to evaluate overall survival (OS) and determine prognostic subclassifications for stage IIIA endometrial cancer. Stage IIIA endometrial cancer patients treated at M.D. Anderson Cancer Center from 1989 to 2002 were reviewed. Clinical information was obtained from the medical record. Cox regression analyses were performed to evaluate the association of pathologic criteria and OS. Patients were divided into four groups based on this analysis: E1, endometrioid/pelvic cytology only; E2, endometrioid/adnexa ± serosal spread; NE1, nonendometrioid/pelvic cytology only; and NE2, nonendometrioid/adenexa ± serosal spread. Forty-nine patients were identified. By multivariate analysis, histology and extent of disease were the only factors associated with OS. Five-year OS in the four subgroups based on histology and extent of disease were: E1, 79%, E2, 65%, NE1, 64%, and NE2, 13%. Histologic subtype and extent of pelvic disease are the only prognostic factors associated with OS. Patients with endometrioid tumors and extent of pelvic disease limited to positive cytology had a favorable outcome, with or without adjuvant therapy. Future prospective clinical trials should consider subclassifying patients with stage IIIA disease to better evaluate the role of adjuvant therapy.</description><subject>Cellular biology</subject><subject>Endometrial cancer</subject><subject>Histology</subject><subject>Medical prognosis</subject><issn>1048-891X</issn><issn>1525-1438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNo9kE1LAzEQhoMoWKv_ISAeV_Ox2U0ED6X4sVDwYsFbyCbZmqW7qUkq9N-bterMYYaZd96BB4AbjG4xptWd6ze6QDkEq-uCIMRyIjSNcHUCZpgRVuCS8tPco5IXXOD3c3ARYz8dESRmYP1ikw1-Y0fr0gH6DsakNhY2TbOAdjR-sCk4tYVaBe1GP6h4D92w2zqtkvNjhJ0PUJl-_6XGBNOHDWp3uARnndpGe_Vb52D99Pi2fClWr8_NcrEqNEG8LDTTllqhTCtqUSFViRYR0qm8bA3VHaqE0YoaXHLcUmwZr2vVcmMN4UjTms7B9dF3F_zn3sYke78PY34pCWNZlO3KrHo4qnTwMQbbyV1wgwoHiZGcSMqJpPwjKf9Jyh-S9BvVUmkF</recordid><startdate>200504</startdate><enddate>200504</enddate><creator>Slomovitz, B.M.</creator><creator>Ramondetta, L.M.</creator><creator>Lee, C.M.</creator><creator>Oh, J.C.</creator><creator>Eifel, P.J.</creator><creator>Jhingran, A.</creator><creator>Burke, T.W.</creator><creator>Gershenson, D.M.</creator><creator>Lu, K.H.</creator><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200504</creationdate><title>Heterogeneity of stage IIIA endometrial carcinomas: implications for adjuvant therapy</title><author>Slomovitz, B.M. ; Ramondetta, L.M. ; Lee, C.M. ; Oh, J.C. ; Eifel, P.J. ; Jhingran, A. ; Burke, T.W. ; Gershenson, D.M. ; Lu, K.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2084-c5ce3e9adb97960a69b022fa208bd3cf069dca3d1481b31e5877ab8ded280c373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Cellular biology</topic><topic>Endometrial cancer</topic><topic>Histology</topic><topic>Medical prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Slomovitz, B.M.</creatorcontrib><creatorcontrib>Ramondetta, L.M.</creatorcontrib><creatorcontrib>Lee, C.M.</creatorcontrib><creatorcontrib>Oh, J.C.</creatorcontrib><creatorcontrib>Eifel, P.J.</creatorcontrib><creatorcontrib>Jhingran, A.</creatorcontrib><creatorcontrib>Burke, T.W.</creatorcontrib><creatorcontrib>Gershenson, D.M.</creatorcontrib><creatorcontrib>Lu, K.H.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>International journal of gynecological cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Slomovitz, B.M.</au><au>Ramondetta, L.M.</au><au>Lee, C.M.</au><au>Oh, J.C.</au><au>Eifel, P.J.</au><au>Jhingran, A.</au><au>Burke, T.W.</au><au>Gershenson, D.M.</au><au>Lu, K.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterogeneity of stage IIIA endometrial carcinomas: implications for adjuvant therapy</atitle><jtitle>International journal of gynecological cancer</jtitle><date>2005-04</date><risdate>2005</risdate><volume>15</volume><issue>3</issue><spage>510</spage><epage>516</epage><pages>510-516</pages><issn>1048-891X</issn><eissn>1525-1438</eissn><abstract>The purpose of this study was to evaluate overall survival (OS) and determine prognostic subclassifications for stage IIIA endometrial cancer. Stage IIIA endometrial cancer patients treated at M.D. Anderson Cancer Center from 1989 to 2002 were reviewed. Clinical information was obtained from the medical record. Cox regression analyses were performed to evaluate the association of pathologic criteria and OS. Patients were divided into four groups based on this analysis: E1, endometrioid/pelvic cytology only; E2, endometrioid/adnexa ± serosal spread; NE1, nonendometrioid/pelvic cytology only; and NE2, nonendometrioid/adenexa ± serosal spread. Forty-nine patients were identified. By multivariate analysis, histology and extent of disease were the only factors associated with OS. Five-year OS in the four subgroups based on histology and extent of disease were: E1, 79%, E2, 65%, NE1, 64%, and NE2, 13%. Histologic subtype and extent of pelvic disease are the only prognostic factors associated with OS. 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subjects | Cellular biology Endometrial cancer Histology Medical prognosis |
title | Heterogeneity of stage IIIA endometrial carcinomas: implications for adjuvant therapy |
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