Carcinosarcoma of the ovary
We report our experience in the management of patients with carcinosarcoma of the ovary, a rare but aggressive variant of ovarian cancer. Forty patients were treated at a single centre, which is the largest reported series. The median age at diagnosis was 65 years (range 45–86) and the median Karnof...
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Veröffentlicht in: | British journal of cancer 2003-03, Vol.88 (5), p.654-657 |
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description | We report our experience in the management of patients with carcinosarcoma of the ovary, a rare but aggressive variant of ovarian cancer. Forty patients were treated at a single centre, which is the largest reported series. The median age at diagnosis was 65 years (range 45–86) and the median Karnofsky performance (KP) status was 70. Thirty-two patients (80%) presented with FIGO stage III or IV disease. Twenty-four had heterologous and 14 homologous carcinosarcoma on review of histopathology, but there was no significant difference in survival between these groups (
P
=0.28). Twenty-seven of the 40 patients had bulk residual disease present after surgery and this was associated with a worse prognosis (
P
=0.045). Chemotherapy was given to 32 patients (80%) of whom 26 (81%) received platinum-based regimens. Of these 32 patients, three (9.4%) achieved a complete response (CR), 10 (31%) a partial response (PR), five (16%) had stable disease, 10 (31%) had progressive disease and four were not assessable. Of the 19 patients who had a CR, PR or stable disease after chemotherapy or were unevaluable (stage Ic), the median survival was 29.6 months. Currently, seven patients are still alive although one has cancer. The overall censored median survival was 8.7 months after a median follow-up of 34 months, and the 1- and 5-year survival were 40 and 7.5%, respectively. |
doi_str_mv | 10.1038/sj.bjc.6600770 |
format | Article |
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P
=0.28). Twenty-seven of the 40 patients had bulk residual disease present after surgery and this was associated with a worse prognosis (
P
=0.045). Chemotherapy was given to 32 patients (80%) of whom 26 (81%) received platinum-based regimens. Of these 32 patients, three (9.4%) achieved a complete response (CR), 10 (31%) a partial response (PR), five (16%) had stable disease, 10 (31%) had progressive disease and four were not assessable. Of the 19 patients who had a CR, PR or stable disease after chemotherapy or were unevaluable (stage Ic), the median survival was 29.6 months. Currently, seven patients are still alive although one has cancer. The overall censored median survival was 8.7 months after a median follow-up of 34 months, and the 1- and 5-year survival were 40 and 7.5%, respectively.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/sj.bjc.6600770</identifier><identifier>PMID: 12618869</identifier><identifier>CODEN: BJCAAI</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Aged ; Aged, 80 and over ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Cancer therapies ; Carcinosarcoma - drug therapy ; Carcinosarcoma - pathology ; Chemotherapy ; Clinical ; Demography ; Disease-Free Survival ; Drug Resistance ; Epidemiology ; Female ; Female genital diseases ; Gynecology ; Gynecology. Andrology. Obstetrics ; Histopathology ; Humans ; Medical prognosis ; Medical research ; Medical sciences ; Middle Aged ; Molecular Medicine ; Oncology ; Ovarian cancer ; Ovarian Neoplasms - drug therapy ; Ovarian Neoplasms - pathology ; Recurrence ; Surgery ; Survival Analysis ; Tumors</subject><ispartof>British journal of cancer, 2003-03, Vol.88 (5), p.654-657</ispartof><rights>The Author(s) 2003</rights><rights>2003 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Mar 10, 2003</rights><rights>Copyright © 2003 Cancer Research UK 2003 Cancer Research UK</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-cf84cebefbed680bd97bc765983e079d3bc237e2a6019652300e96bfa6a5b9dc3</citedby><cites>FETCH-LOGICAL-c483t-cf84cebefbed680bd97bc765983e079d3bc237e2a6019652300e96bfa6a5b9dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376340/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376340/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14617002$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12618869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harris, M A</creatorcontrib><creatorcontrib>Delap, L M</creatorcontrib><creatorcontrib>Sengupta, P S</creatorcontrib><creatorcontrib>Wilkinson, P M</creatorcontrib><creatorcontrib>Welch, R S</creatorcontrib><creatorcontrib>Swindell, R</creatorcontrib><creatorcontrib>Shanks, J H</creatorcontrib><creatorcontrib>Wilson, G</creatorcontrib><creatorcontrib>Slade, R J</creatorcontrib><creatorcontrib>Reynolds, K</creatorcontrib><creatorcontrib>Jayson, G C</creatorcontrib><title>Carcinosarcoma of the ovary</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>We report our experience in the management of patients with carcinosarcoma of the ovary, a rare but aggressive variant of ovarian cancer. Forty patients were treated at a single centre, which is the largest reported series. The median age at diagnosis was 65 years (range 45–86) and the median Karnofsky performance (KP) status was 70. Thirty-two patients (80%) presented with FIGO stage III or IV disease. Twenty-four had heterologous and 14 homologous carcinosarcoma on review of histopathology, but there was no significant difference in survival between these groups (
P
=0.28). Twenty-seven of the 40 patients had bulk residual disease present after surgery and this was associated with a worse prognosis (
P
=0.045). Chemotherapy was given to 32 patients (80%) of whom 26 (81%) received platinum-based regimens. Of these 32 patients, three (9.4%) achieved a complete response (CR), 10 (31%) a partial response (PR), five (16%) had stable disease, 10 (31%) had progressive disease and four were not assessable. Of the 19 patients who had a CR, PR or stable disease after chemotherapy or were unevaluable (stage Ic), the median survival was 29.6 months. Currently, seven patients are still alive although one has cancer. The overall censored median survival was 8.7 months after a median follow-up of 34 months, and the 1- and 5-year survival were 40 and 7.5%, respectively.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Cancer therapies</subject><subject>Carcinosarcoma - drug therapy</subject><subject>Carcinosarcoma - pathology</subject><subject>Chemotherapy</subject><subject>Clinical</subject><subject>Demography</subject><subject>Disease-Free Survival</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Gynecology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Histopathology</subject><subject>Humans</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Medicine</subject><subject>Oncology</subject><subject>Ovarian cancer</subject><subject>Ovarian Neoplasms - drug therapy</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Recurrence</subject><subject>Surgery</subject><subject>Survival Analysis</subject><subject>Tumors</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kM1LAzEQxYMotlavXgQpgt62nSS7-bgIUvwCwYueQ5LNtrtsNzVpBf97I12sCp6Gyfzy5s1D6BTDBAMV09hMTGMnjAFwDntoiAtKMiwI30dDSI8ZSAIDdBRjk1oJgh-iASYMC8HkEJ3NdLB152MqfqnHvhqvF27s33X4OEYHlW6jO-nrCL3e3b7MHrKn5_vH2c1TZnNB15mtRG6dcZVxJRNgSsmN5ayQgjrgsqTGEsod0QywZAWhAE4yU2mmCyNLS0foequ72pilK63r1kG3ahXqZXKhvK7V70lXL9Tcv6sky2gOSeCqFwj-bePiWi3raF3b6s75TVScgmAFyARe_AEbvwldOk4RApgxkdMETbaQDT7G4KpvJxjUV-gqNiqFrvrQ04fzn_53eJ9yAi57QEer2yroztZxx-UMcwCSuOmWi2nUzV3Y2ftn9Sel1poo</recordid><startdate>20030310</startdate><enddate>20030310</enddate><creator>Harris, M A</creator><creator>Delap, L M</creator><creator>Sengupta, P S</creator><creator>Wilkinson, P M</creator><creator>Welch, R S</creator><creator>Swindell, R</creator><creator>Shanks, J H</creator><creator>Wilson, G</creator><creator>Slade, R J</creator><creator>Reynolds, K</creator><creator>Jayson, G C</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>IQODW</scope><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>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030310</creationdate><title>Carcinosarcoma of the ovary</title><author>Harris, M A ; Delap, L M ; Sengupta, P S ; Wilkinson, P M ; Welch, R S ; Swindell, R ; Shanks, J H ; Wilson, G ; Slade, R J ; Reynolds, K ; Jayson, G C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-cf84cebefbed680bd97bc765983e079d3bc237e2a6019652300e96bfa6a5b9dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Cancer therapies</topic><topic>Carcinosarcoma - drug therapy</topic><topic>Carcinosarcoma - pathology</topic><topic>Chemotherapy</topic><topic>Clinical</topic><topic>Demography</topic><topic>Disease-Free Survival</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Gynecology</topic><topic>Gynecology. 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Forty patients were treated at a single centre, which is the largest reported series. The median age at diagnosis was 65 years (range 45–86) and the median Karnofsky performance (KP) status was 70. Thirty-two patients (80%) presented with FIGO stage III or IV disease. Twenty-four had heterologous and 14 homologous carcinosarcoma on review of histopathology, but there was no significant difference in survival between these groups (
P
=0.28). Twenty-seven of the 40 patients had bulk residual disease present after surgery and this was associated with a worse prognosis (
P
=0.045). Chemotherapy was given to 32 patients (80%) of whom 26 (81%) received platinum-based regimens. Of these 32 patients, three (9.4%) achieved a complete response (CR), 10 (31%) a partial response (PR), five (16%) had stable disease, 10 (31%) had progressive disease and four were not assessable. Of the 19 patients who had a CR, PR or stable disease after chemotherapy or were unevaluable (stage Ic), the median survival was 29.6 months. Currently, seven patients are still alive although one has cancer. The overall censored median survival was 8.7 months after a median follow-up of 34 months, and the 1- and 5-year survival were 40 and 7.5%, respectively.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>12618869</pmid><doi>10.1038/sj.bjc.6600770</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Antineoplastic Agents - administration & dosage Antineoplastic Agents - therapeutic use Biological and medical sciences Biomedical and Life Sciences Biomedicine Cancer Research Cancer therapies Carcinosarcoma - drug therapy Carcinosarcoma - pathology Chemotherapy Clinical Demography Disease-Free Survival Drug Resistance Epidemiology Female Female genital diseases Gynecology Gynecology. Andrology. Obstetrics Histopathology Humans Medical prognosis Medical research Medical sciences Middle Aged Molecular Medicine Oncology Ovarian cancer Ovarian Neoplasms - drug therapy Ovarian Neoplasms - pathology Recurrence Surgery Survival Analysis Tumors |
title | Carcinosarcoma of the ovary |
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