Survival of children with soft-tissue sarcoma in Europe since 1978: results from the EUROCARE study
Soft-tissue sarcomas account for 5–8% of all childhood cancers in European countries. In the EUROCARE childhood cancer study, there were 2163 registrations from 17 countries for soft-tissue sarcomas in patients aged 0–14 years during 1978–1989. Of this total, three-quarters were contributed by child...
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Veröffentlicht in: | European journal of cancer (1990) 2001-04, Vol.37 (6), p.767-774 |
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description | Soft-tissue sarcomas account for 5–8% of all childhood cancers in European countries. In the EUROCARE childhood cancer study, there were 2163 registrations from 17 countries for soft-tissue sarcomas in patients aged 0–14 years during 1978–1989. Of this total, three-quarters were contributed by childhood cancer registries in Germany and the UK. Age-standardised 5-year survival rates of children diagnosed during 1985–1989 were 65% (95% confidence interval (CI) 56–72) for rhabdomyosarcoma, 68% (95% CI 58–77) for fibrosarcoma, 78% (95% CI: 64–87) for other specified soft-tissue sarcomas except Kaposi's and 51% (95% CI 37–65) for ‘unspecified’ soft-tissue sarcomas. Survival rates increased steadily throughout the 12-year study period for all soft-tissue sarcomas combined, but the increase took place predominantly in the early 1980s for rhabdomyosarcoma. Improvements in survival which had previously been reported from individual countries and in clinical series are confirmed as having taken place throughout much of Europe on a population basis. In a supplementary analysis, there was little indication of a further improvement during 1990–1992. |
doi_str_mv | 10.1016/S0959-8049(01)00007-7 |
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In the EUROCARE childhood cancer study, there were 2163 registrations from 17 countries for soft-tissue sarcomas in patients aged 0–14 years during 1978–1989. Of this total, three-quarters were contributed by childhood cancer registries in Germany and the UK. Age-standardised 5-year survival rates of children diagnosed during 1985–1989 were 65% (95% confidence interval (CI) 56–72) for rhabdomyosarcoma, 68% (95% CI 58–77) for fibrosarcoma, 78% (95% CI: 64–87) for other specified soft-tissue sarcomas except Kaposi's and 51% (95% CI 37–65) for ‘unspecified’ soft-tissue sarcomas. Survival rates increased steadily throughout the 12-year study period for all soft-tissue sarcomas combined, but the increase took place predominantly in the early 1980s for rhabdomyosarcoma. Improvements in survival which had previously been reported from individual countries and in clinical series are confirmed as having taken place throughout much of Europe on a population basis. In a supplementary analysis, there was little indication of a further improvement during 1990–1992.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/S0959-8049(01)00007-7</identifier><identifier>PMID: 11311652</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adolescent ; Cancer registries ; Child ; Child, Preschool ; Children ; Europe ; Europe - epidemiology ; Female ; Fibrosarcoma ; Fibrosarcoma - mortality ; Humans ; Incidence ; Infant ; Infant, Newborn ; Male ; Multivariate Analysis ; Population-based survival ; Proportional Hazards Models ; Registries ; Rhabdomyosarcoma ; Rhabdomyosarcoma - mortality ; Sarcoma - mortality ; Soft-tissue neoplasms ; Survival Analysis ; Survival Rate - trends ; Survival trends</subject><ispartof>European journal of cancer (1990), 2001-04, Vol.37 (6), p.767-774</ispartof><rights>2001 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0959-8049(01)00007-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11311652$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stiller, C.A</creatorcontrib><creatorcontrib>Stevens, M.C.G</creatorcontrib><creatorcontrib>Magnani, C</creatorcontrib><creatorcontrib>Corazziari, I</creatorcontrib><creatorcontrib>EUROCARE Working Group</creatorcontrib><title>Survival of children with soft-tissue sarcoma in Europe since 1978: results from the EUROCARE study</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Soft-tissue sarcomas account for 5–8% of all childhood cancers in European countries. In the EUROCARE childhood cancer study, there were 2163 registrations from 17 countries for soft-tissue sarcomas in patients aged 0–14 years during 1978–1989. Of this total, three-quarters were contributed by childhood cancer registries in Germany and the UK. Age-standardised 5-year survival rates of children diagnosed during 1985–1989 were 65% (95% confidence interval (CI) 56–72) for rhabdomyosarcoma, 68% (95% CI 58–77) for fibrosarcoma, 78% (95% CI: 64–87) for other specified soft-tissue sarcomas except Kaposi's and 51% (95% CI 37–65) for ‘unspecified’ soft-tissue sarcomas. Survival rates increased steadily throughout the 12-year study period for all soft-tissue sarcomas combined, but the increase took place predominantly in the early 1980s for rhabdomyosarcoma. Improvements in survival which had previously been reported from individual countries and in clinical series are confirmed as having taken place throughout much of Europe on a population basis. In a supplementary analysis, there was little indication of a further improvement during 1990–1992.</description><subject>Adolescent</subject><subject>Cancer registries</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Europe</subject><subject>Europe - epidemiology</subject><subject>Female</subject><subject>Fibrosarcoma</subject><subject>Fibrosarcoma - mortality</subject><subject>Humans</subject><subject>Incidence</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Multivariate Analysis</subject><subject>Population-based survival</subject><subject>Proportional Hazards Models</subject><subject>Registries</subject><subject>Rhabdomyosarcoma</subject><subject>Rhabdomyosarcoma - mortality</subject><subject>Sarcoma - mortality</subject><subject>Soft-tissue neoplasms</subject><subject>Survival Analysis</subject><subject>Survival Rate - trends</subject><subject>Survival trends</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kV1L7DAQhoMoukf9CUquRC-qk6bNhzeyLHuOgiD4cR2yyZSNtNs1SVf893bV49wMDA_DzPsQcsLgkgETV0-ga10oqPQ5sAsYSxZyh0yYkroAVZe7ZPKLHJA_Kb1uGVXBPjlgjDMm6nJC3NMQN2FjW9o31C1D6yOu6HvIS5r6Jhc5pDQgTTa6vrM0rOh8iP16nISVQ8q0VNc0YhranGgT-47mJdL5y-PDbPo4pykP_uOI7DW2TXj80w_Jy9_58-y2uH_4dzeb3hdYCp6LSjrG5KIusVbCC1QcygXnnmtwinulNWrHLYB3wloUgBIq18imcU5WXPBDcva9dx37twFTNl1IDtvWrrAfkpEShJSlGsHTH3BYdOjNOobOxg_zP5YRuPkGcDx3EzCa5AKOD_sQ0WXj-2AYmK0I8yXCbFM2wMyXCCP5J3fkeMg</recordid><startdate>20010401</startdate><enddate>20010401</enddate><creator>Stiller, C.A</creator><creator>Stevens, M.C.G</creator><creator>Magnani, C</creator><creator>Corazziari, I</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20010401</creationdate><title>Survival of children with soft-tissue sarcoma in Europe since 1978: results from the EUROCARE study</title><author>Stiller, C.A ; Stevens, M.C.G ; Magnani, C ; Corazziari, I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e263t-47c117b52e586d6e8302b33d390c83d899e9c3a00dc6aae60e704cf7ffcc74363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adolescent</topic><topic>Cancer registries</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Europe</topic><topic>Europe - epidemiology</topic><topic>Female</topic><topic>Fibrosarcoma</topic><topic>Fibrosarcoma - mortality</topic><topic>Humans</topic><topic>Incidence</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Multivariate Analysis</topic><topic>Population-based survival</topic><topic>Proportional Hazards Models</topic><topic>Registries</topic><topic>Rhabdomyosarcoma</topic><topic>Rhabdomyosarcoma - mortality</topic><topic>Sarcoma - mortality</topic><topic>Soft-tissue neoplasms</topic><topic>Survival Analysis</topic><topic>Survival Rate - trends</topic><topic>Survival trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stiller, C.A</creatorcontrib><creatorcontrib>Stevens, M.C.G</creatorcontrib><creatorcontrib>Magnani, C</creatorcontrib><creatorcontrib>Corazziari, I</creatorcontrib><creatorcontrib>EUROCARE Working Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stiller, C.A</au><au>Stevens, M.C.G</au><au>Magnani, C</au><au>Corazziari, I</au><aucorp>EUROCARE Working Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Survival of children with soft-tissue sarcoma in Europe since 1978: results from the EUROCARE study</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2001-04-01</date><risdate>2001</risdate><volume>37</volume><issue>6</issue><spage>767</spage><epage>774</epage><pages>767-774</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Soft-tissue sarcomas account for 5–8% of all childhood cancers in European countries. In the EUROCARE childhood cancer study, there were 2163 registrations from 17 countries for soft-tissue sarcomas in patients aged 0–14 years during 1978–1989. Of this total, three-quarters were contributed by childhood cancer registries in Germany and the UK. Age-standardised 5-year survival rates of children diagnosed during 1985–1989 were 65% (95% confidence interval (CI) 56–72) for rhabdomyosarcoma, 68% (95% CI 58–77) for fibrosarcoma, 78% (95% CI: 64–87) for other specified soft-tissue sarcomas except Kaposi's and 51% (95% CI 37–65) for ‘unspecified’ soft-tissue sarcomas. Survival rates increased steadily throughout the 12-year study period for all soft-tissue sarcomas combined, but the increase took place predominantly in the early 1980s for rhabdomyosarcoma. Improvements in survival which had previously been reported from individual countries and in clinical series are confirmed as having taken place throughout much of Europe on a population basis. In a supplementary analysis, there was little indication of a further improvement during 1990–1992.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>11311652</pmid><doi>10.1016/S0959-8049(01)00007-7</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Cancer registries Child Child, Preschool Children Europe Europe - epidemiology Female Fibrosarcoma Fibrosarcoma - mortality Humans Incidence Infant Infant, Newborn Male Multivariate Analysis Population-based survival Proportional Hazards Models Registries Rhabdomyosarcoma Rhabdomyosarcoma - mortality Sarcoma - mortality Soft-tissue neoplasms Survival Analysis Survival Rate - trends Survival trends |
title | Survival of children with soft-tissue sarcoma in Europe since 1978: results from the EUROCARE study |
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