Adjuvant platinum-based chemotherapy for borderline serous ovarian tumors with invasive implants

Abstract Background Most borderline ovarian tumors (BOTs) are cured with surgery. However BOTs with invasive implants have a poor prognosis with a mortality of 20–40%. The benefit of adjuvant chemotherapy (CT) in this setting remains poorly defined. Methods Retrospective study of serous BOT + invasi...

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Veröffentlicht in:Gynecologic oncology 2014-01, Vol.132 (1), p.23-27
Hauptverfasser: Leary, Alexandra, Petrella, Marie Christina, Pautier, Patricia, Duvillard, Pierre, Uzan, Catherine, Tazi, Youssef, Ledoux, Florence, Gouy, Sébastien, Morice, Philippe, Lhommé, Catherine
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container_end_page 27
container_issue 1
container_start_page 23
container_title Gynecologic oncology
container_volume 132
creator Leary, Alexandra
Petrella, Marie Christina
Pautier, Patricia
Duvillard, Pierre
Uzan, Catherine
Tazi, Youssef
Ledoux, Florence
Gouy, Sébastien
Morice, Philippe
Lhommé, Catherine
description Abstract Background Most borderline ovarian tumors (BOTs) are cured with surgery. However BOTs with invasive implants have a poor prognosis with a mortality of 20–40%. The benefit of adjuvant chemotherapy (CT) in this setting remains poorly defined. Methods Retrospective study of serous BOT + invasive implants treated with adjuvant CT. Results 36 patients were referred with serous BOTs + invasive implants and treated with surgery and platinum-based CT between 06/1982 and 02/2011. 83% were stage III/IV. Tumors demonstrated microinvasion, micropapillary pattern or desmoplastic implants in 53%, 47% and 67% of cases, respectively. 8% had fertility-sparing surgery. Taking into account initial and completion surgeries, R0 was achieved in 84% (27/32) (NA, N = 4). The majority (72%) received a combination of platinum + taxane. 11% of patients experienced a G3/G4 toxicity. 13 of 36 (36%) patients relapsed at a median of 27.3 months after diagnosis of invasive implants. Among 12 patients with histologically confirmed relapse, 8 patients progressed with invasive disease in the form of carcinoma or invasive implants. 5 year PFS/OS were 67%/96%. Neither microinvasion, micropapillary pattern, nor desmoplastic implants predicted relapse. In cases with evaluable disease, an objective response to chemotherapy was observed in 4 of 6 patients. Conclusion This is the largest study of BOT with invasive implants treated with surgery and adjuvant platinum-based CT. Treatment was well tolerated and the invasive relapse rate was 22% (8/36). Although numbers are small, the objective responses suggest a possible role for adjuvant CT in BOTs with invasive implants.
doi_str_mv 10.1016/j.ygyno.2013.11.006
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However BOTs with invasive implants have a poor prognosis with a mortality of 20–40%. The benefit of adjuvant chemotherapy (CT) in this setting remains poorly defined. Methods Retrospective study of serous BOT + invasive implants treated with adjuvant CT. Results 36 patients were referred with serous BOTs + invasive implants and treated with surgery and platinum-based CT between 06/1982 and 02/2011. 83% were stage III/IV. Tumors demonstrated microinvasion, micropapillary pattern or desmoplastic implants in 53%, 47% and 67% of cases, respectively. 8% had fertility-sparing surgery. Taking into account initial and completion surgeries, R0 was achieved in 84% (27/32) (NA, N = 4). The majority (72%) received a combination of platinum + taxane. 11% of patients experienced a G3/G4 toxicity. 13 of 36 (36%) patients relapsed at a median of 27.3 months after diagnosis of invasive implants. Among 12 patients with histologically confirmed relapse, 8 patients progressed with invasive disease in the form of carcinoma or invasive implants. 5 year PFS/OS were 67%/96%. Neither microinvasion, micropapillary pattern, nor desmoplastic implants predicted relapse. In cases with evaluable disease, an objective response to chemotherapy was observed in 4 of 6 patients. Conclusion This is the largest study of BOT with invasive implants treated with surgery and adjuvant platinum-based CT. Treatment was well tolerated and the invasive relapse rate was 22% (8/36). Although numbers are small, the objective responses suggest a possible role for adjuvant CT in BOTs with invasive implants.</description><identifier>ISSN: 0090-8258</identifier><identifier>EISSN: 1095-6859</identifier><identifier>DOI: 10.1016/j.ygyno.2013.11.006</identifier><identifier>PMID: 24219980</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adjuvant chemotherapy ; Adolescent ; Adult ; Aged ; Antineoplastic Agents - therapeutic use ; Chemotherapy, Adjuvant ; Cystadenocarcinoma, Serous - drug therapy ; Cystadenocarcinoma, Serous - mortality ; Cystadenocarcinoma, Serous - pathology ; Female ; Hematology, Oncology and Palliative Medicine ; Humans ; Invasive implants ; Middle Aged ; Neoplasm Staging ; Obstetrics and Gynecology ; Ovarian Neoplasms - drug therapy ; Ovarian Neoplasms - mortality ; Ovarian Neoplasms - pathology ; Platinum - therapeutic use ; Retrospective Studies ; Serous borderline ovarian tumor ; Treatment Outcome</subject><ispartof>Gynecologic oncology, 2014-01, Vol.132 (1), p.23-27</ispartof><rights>2013</rights><rights>Copyright © 2013. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-51d812a6add8603bd49ecff593b6185efec42a9df3719746171d0e748025c19e3</citedby><cites>FETCH-LOGICAL-c414t-51d812a6add8603bd49ecff593b6185efec42a9df3719746171d0e748025c19e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ygyno.2013.11.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24219980$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leary, Alexandra</creatorcontrib><creatorcontrib>Petrella, Marie Christina</creatorcontrib><creatorcontrib>Pautier, Patricia</creatorcontrib><creatorcontrib>Duvillard, Pierre</creatorcontrib><creatorcontrib>Uzan, Catherine</creatorcontrib><creatorcontrib>Tazi, Youssef</creatorcontrib><creatorcontrib>Ledoux, Florence</creatorcontrib><creatorcontrib>Gouy, Sébastien</creatorcontrib><creatorcontrib>Morice, Philippe</creatorcontrib><creatorcontrib>Lhommé, Catherine</creatorcontrib><title>Adjuvant platinum-based chemotherapy for borderline serous ovarian tumors with invasive implants</title><title>Gynecologic oncology</title><addtitle>Gynecol Oncol</addtitle><description>Abstract Background Most borderline ovarian tumors (BOTs) are cured with surgery. However BOTs with invasive implants have a poor prognosis with a mortality of 20–40%. The benefit of adjuvant chemotherapy (CT) in this setting remains poorly defined. Methods Retrospective study of serous BOT + invasive implants treated with adjuvant CT. Results 36 patients were referred with serous BOTs + invasive implants and treated with surgery and platinum-based CT between 06/1982 and 02/2011. 83% were stage III/IV. Tumors demonstrated microinvasion, micropapillary pattern or desmoplastic implants in 53%, 47% and 67% of cases, respectively. 8% had fertility-sparing surgery. Taking into account initial and completion surgeries, R0 was achieved in 84% (27/32) (NA, N = 4). The majority (72%) received a combination of platinum + taxane. 11% of patients experienced a G3/G4 toxicity. 13 of 36 (36%) patients relapsed at a median of 27.3 months after diagnosis of invasive implants. Among 12 patients with histologically confirmed relapse, 8 patients progressed with invasive disease in the form of carcinoma or invasive implants. 5 year PFS/OS were 67%/96%. Neither microinvasion, micropapillary pattern, nor desmoplastic implants predicted relapse. In cases with evaluable disease, an objective response to chemotherapy was observed in 4 of 6 patients. Conclusion This is the largest study of BOT with invasive implants treated with surgery and adjuvant platinum-based CT. Treatment was well tolerated and the invasive relapse rate was 22% (8/36). Although numbers are small, the objective responses suggest a possible role for adjuvant CT in BOTs with invasive implants.</description><subject>Adjuvant chemotherapy</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Chemotherapy, Adjuvant</subject><subject>Cystadenocarcinoma, Serous - drug therapy</subject><subject>Cystadenocarcinoma, Serous - mortality</subject><subject>Cystadenocarcinoma, Serous - pathology</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Invasive implants</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Obstetrics and Gynecology</subject><subject>Ovarian Neoplasms - drug therapy</subject><subject>Ovarian Neoplasms - mortality</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Platinum - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Serous borderline ovarian tumor</subject><subject>Treatment Outcome</subject><issn>0090-8258</issn><issn>1095-6859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0EokvhEyAhH7kkzOTfxgeQqgpopUo9UM7GsSesQxIvdpIq374OWzhw6Wku772Z-T3G3iKkCFh96NL15zq6NAPMU8QUoHrGdgiiTKq6FM_ZDkBAUmdlfcZehdABQA6YvWRnWZGhEDXs2I8L082LGid-7NVkx3lIGhXIcH2gwU0H8uq48tZ53jhvyPd2JB7Iuzlwtyhv1cineXA-8Hs7HbgdFxXsQtwOMXCcwmv2olV9oDeP85x9__L57vIqubn9en15cZPoAospKdHUmKlKGVNXkDemEKTbthR5U2FdUku6yJQwbb5HsS8q3KMB2hc1ZKVGQfk5e3_KPXr3e6YwycEGTX08guKxEguBUEF8PErzk1R7F4KnVh69HZRfJYLc0MpO_kErN7QSUUa00fXuccHcDGT-ef6yjIKPJwHFNxdLXgZtadRkrCc9SePsEws-_efXkbbVqv9FK4XOzX6MBCXKkEmQ37Z2t3JxK1XkVf4AI7qiIw</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Leary, Alexandra</creator><creator>Petrella, Marie Christina</creator><creator>Pautier, Patricia</creator><creator>Duvillard, Pierre</creator><creator>Uzan, Catherine</creator><creator>Tazi, Youssef</creator><creator>Ledoux, Florence</creator><creator>Gouy, Sébastien</creator><creator>Morice, Philippe</creator><creator>Lhommé, Catherine</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>20140101</creationdate><title>Adjuvant platinum-based chemotherapy for borderline serous ovarian tumors with invasive implants</title><author>Leary, Alexandra ; Petrella, Marie Christina ; Pautier, Patricia ; Duvillard, Pierre ; Uzan, Catherine ; Tazi, Youssef ; Ledoux, Florence ; Gouy, Sébastien ; Morice, Philippe ; Lhommé, Catherine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-51d812a6add8603bd49ecff593b6185efec42a9df3719746171d0e748025c19e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adjuvant chemotherapy</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Chemotherapy, Adjuvant</topic><topic>Cystadenocarcinoma, Serous - drug therapy</topic><topic>Cystadenocarcinoma, Serous - mortality</topic><topic>Cystadenocarcinoma, Serous - pathology</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Invasive implants</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Obstetrics and Gynecology</topic><topic>Ovarian Neoplasms - drug therapy</topic><topic>Ovarian Neoplasms - mortality</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Platinum - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Serous borderline ovarian tumor</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leary, Alexandra</creatorcontrib><creatorcontrib>Petrella, Marie Christina</creatorcontrib><creatorcontrib>Pautier, Patricia</creatorcontrib><creatorcontrib>Duvillard, Pierre</creatorcontrib><creatorcontrib>Uzan, Catherine</creatorcontrib><creatorcontrib>Tazi, Youssef</creatorcontrib><creatorcontrib>Ledoux, Florence</creatorcontrib><creatorcontrib>Gouy, Sébastien</creatorcontrib><creatorcontrib>Morice, Philippe</creatorcontrib><creatorcontrib>Lhommé, Catherine</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>Leary, Alexandra</au><au>Petrella, Marie Christina</au><au>Pautier, Patricia</au><au>Duvillard, Pierre</au><au>Uzan, Catherine</au><au>Tazi, Youssef</au><au>Ledoux, Florence</au><au>Gouy, Sébastien</au><au>Morice, Philippe</au><au>Lhommé, Catherine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adjuvant platinum-based chemotherapy for borderline serous ovarian tumors with invasive implants</atitle><jtitle>Gynecologic oncology</jtitle><addtitle>Gynecol Oncol</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>132</volume><issue>1</issue><spage>23</spage><epage>27</epage><pages>23-27</pages><issn>0090-8258</issn><eissn>1095-6859</eissn><abstract>Abstract Background Most borderline ovarian tumors (BOTs) are cured with surgery. However BOTs with invasive implants have a poor prognosis with a mortality of 20–40%. The benefit of adjuvant chemotherapy (CT) in this setting remains poorly defined. Methods Retrospective study of serous BOT + invasive implants treated with adjuvant CT. Results 36 patients were referred with serous BOTs + invasive implants and treated with surgery and platinum-based CT between 06/1982 and 02/2011. 83% were stage III/IV. Tumors demonstrated microinvasion, micropapillary pattern or desmoplastic implants in 53%, 47% and 67% of cases, respectively. 8% had fertility-sparing surgery. Taking into account initial and completion surgeries, R0 was achieved in 84% (27/32) (NA, N = 4). The majority (72%) received a combination of platinum + taxane. 11% of patients experienced a G3/G4 toxicity. 13 of 36 (36%) patients relapsed at a median of 27.3 months after diagnosis of invasive implants. Among 12 patients with histologically confirmed relapse, 8 patients progressed with invasive disease in the form of carcinoma or invasive implants. 5 year PFS/OS were 67%/96%. Neither microinvasion, micropapillary pattern, nor desmoplastic implants predicted relapse. In cases with evaluable disease, an objective response to chemotherapy was observed in 4 of 6 patients. Conclusion This is the largest study of BOT with invasive implants treated with surgery and adjuvant platinum-based CT. Treatment was well tolerated and the invasive relapse rate was 22% (8/36). Although numbers are small, the objective responses suggest a possible role for adjuvant CT in BOTs with invasive implants.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24219980</pmid><doi>10.1016/j.ygyno.2013.11.006</doi><tpages>5</tpages></addata></record>
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subjects Adjuvant chemotherapy
Adolescent
Adult
Aged
Antineoplastic Agents - therapeutic use
Chemotherapy, Adjuvant
Cystadenocarcinoma, Serous - drug therapy
Cystadenocarcinoma, Serous - mortality
Cystadenocarcinoma, Serous - pathology
Female
Hematology, Oncology and Palliative Medicine
Humans
Invasive implants
Middle Aged
Neoplasm Staging
Obstetrics and Gynecology
Ovarian Neoplasms - drug therapy
Ovarian Neoplasms - mortality
Ovarian Neoplasms - pathology
Platinum - therapeutic use
Retrospective Studies
Serous borderline ovarian tumor
Treatment Outcome
title Adjuvant platinum-based chemotherapy for borderline serous ovarian tumors with invasive implants
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