Multivariate analysis for clinical prognostic factors in 163 patients with soft tissue sarcoma
Clinical and histologic findings in 163 patients with localized soft tissue sarcoma (STS) in the extremities and trunk were reviewed. There were 91 male patients and 72 female patients ranging in age from 2 to 84 years (median, 46 years). The histologic status of the tumors was as follows: low grade...
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Veröffentlicht in: | Cancer 1988-10, Vol.62 (7), p.1444-1450 |
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description | Clinical and histologic findings in 163 patients with localized soft tissue sarcoma (STS) in the extremities and trunk were reviewed. There were 91 male patients and 72 female patients ranging in age from 2 to 84 years (median, 46 years). The histologic status of the tumors was as follows: low grade, 29 cases; intermediate grade, 52 cases; and high grade, 82 cases. The primary tumors were treated by intralesional excision (two cases), marginal (88), wide local (52), or amputation (21). Subsequent adjuvant therapy was given to 61 patients; 17 had radiotherapy (RT), 27 had chemotherapy (CH), and 17 had combined RT and CH. The overall survival (P < 0.1) and disease‐free survival (P < 0.001) were better in the group that received multimodal treatment (radical surgery and adjuvant chemotherapy with or without radiotherapy) than in the group treated only by surgery. This suggests the favorable role of adjuvant therapy. The univariate and the Cox multivariate analysis for prognosis revealed that sex, tumor‐related symptoms, tumor size, tumor depth, and histologic grade were the significant factors. Among the treatment schemes, adjuvant chemotherapy was the only one that affected survival, especially for the intermediate‐grade tumors. Initial surgical treatment (marginal versus wide local excision) significantly contributed to the local control of the primary tumors. |
doi_str_mv | 10.1002/1097-0142(19881001)62:7<1444::AID-CNCR2820620733>3.0.CO;2-L |
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There were 91 male patients and 72 female patients ranging in age from 2 to 84 years (median, 46 years). The histologic status of the tumors was as follows: low grade, 29 cases; intermediate grade, 52 cases; and high grade, 82 cases. The primary tumors were treated by intralesional excision (two cases), marginal (88), wide local (52), or amputation (21). Subsequent adjuvant therapy was given to 61 patients; 17 had radiotherapy (RT), 27 had chemotherapy (CH), and 17 had combined RT and CH. The overall survival (P < 0.1) and disease‐free survival (P < 0.001) were better in the group that received multimodal treatment (radical surgery and adjuvant chemotherapy with or without radiotherapy) than in the group treated only by surgery. This suggests the favorable role of adjuvant therapy. The univariate and the Cox multivariate analysis for prognosis revealed that sex, tumor‐related symptoms, tumor size, tumor depth, and histologic grade were the significant factors. Among the treatment schemes, adjuvant chemotherapy was the only one that affected survival, especially for the intermediate‐grade tumors. Initial surgical treatment (marginal versus wide local excision) significantly contributed to the local control of the primary tumors.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19881001)62:7<1444::AID-CNCR2820620733>3.0.CO;2-L</identifier><identifier>PMID: 3416283</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Actuarial Analysis ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Child ; Child, Preschool ; Combined Modality Therapy ; Female ; Humans ; Infant ; Male ; Medical sciences ; Middle Aged ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Prognosis ; Sarcoma - pathology ; Sarcoma - surgery ; Sex Factors ; Soft Tissue Neoplasms - pathology ; Soft Tissue Neoplasms - surgery ; Statistics as Topic ; Tumors</subject><ispartof>Cancer, 1988-10, Vol.62 (7), p.1444-1450</ispartof><rights>Copyright © 1988 American Cancer Society</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4983-7f63067d44b271185287e3025dee94194fde72b4c84feb108b496e5042bba583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7817312$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3416283$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ueda, Takafumi</creatorcontrib><creatorcontrib>Aozasa, Katsuyuki</creatorcontrib><creatorcontrib>Tsujimoto, Masahiko</creatorcontrib><creatorcontrib>Hamada, Hideki</creatorcontrib><creatorcontrib>Hayashi, Hideki</creatorcontrib><creatorcontrib>Ono, Keiro</creatorcontrib><creatorcontrib>Matsumoto, Keishi</creatorcontrib><title>Multivariate analysis for clinical prognostic factors in 163 patients with soft tissue sarcoma</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Clinical and histologic findings in 163 patients with localized soft tissue sarcoma (STS) in the extremities and trunk were reviewed. There were 91 male patients and 72 female patients ranging in age from 2 to 84 years (median, 46 years). The histologic status of the tumors was as follows: low grade, 29 cases; intermediate grade, 52 cases; and high grade, 82 cases. The primary tumors were treated by intralesional excision (two cases), marginal (88), wide local (52), or amputation (21). Subsequent adjuvant therapy was given to 61 patients; 17 had radiotherapy (RT), 27 had chemotherapy (CH), and 17 had combined RT and CH. The overall survival (P < 0.1) and disease‐free survival (P < 0.001) were better in the group that received multimodal treatment (radical surgery and adjuvant chemotherapy with or without radiotherapy) than in the group treated only by surgery. This suggests the favorable role of adjuvant therapy. The univariate and the Cox multivariate analysis for prognosis revealed that sex, tumor‐related symptoms, tumor size, tumor depth, and histologic grade were the significant factors. Among the treatment schemes, adjuvant chemotherapy was the only one that affected survival, especially for the intermediate‐grade tumors. Initial surgical treatment (marginal versus wide local excision) significantly contributed to the local control of the primary tumors.</description><subject>Actuarial Analysis</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Prognosis</subject><subject>Sarcoma - pathology</subject><subject>Sarcoma - surgery</subject><subject>Sex Factors</subject><subject>Soft Tissue Neoplasms - pathology</subject><subject>Soft Tissue Neoplasms - surgery</subject><subject>Statistics as Topic</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF2LEzEYhYMoa3f1Jwi5ENGLqW8-ZpKpIizj10K1IHshCIZMmmhkOlPzZnbpv3dKa0EvBK9Ccp4cDg8hDYM5A-DPGdSqACb5U1ZrPT2xZxVfqJdMSrlYXF69LpqPzSeuOVQclBCvxBzmzeoFL5Z3yOz0-y6ZAYAuSik-3yfniD-mq-KlOCNnQrKKazEjXz-MXY43NkWbPbW97XYYkYYhUdfFPjrb0W0avvUD5uhosC4PCWnsKasE3docfZ-R3sb8neIQMs0RcfQUbXLDxj4g94Lt0D88nhfk-u2b6-Z9sVy9u2oul4WTtRaFCpWASq2lbLliTJdcKy-Al2vva8lqGdZe8VY6LYNvGehW1pUvQfK2taUWF-TJoXaa-nP0mM0movNdZ3s_jGiUlsA1iAn8cgBdGhCTD2ab4samnWFg9vLNXp_Z6zO_5ZuKG2X28o2Z5Js_5RthwDQrw81yan90nDG2G78-dR9tT_njY25xEhuS7V3EE6Y0U4LxCQsH7DZ2fvd_C_858K9E_AKKVK5Z</recordid><startdate>19881001</startdate><enddate>19881001</enddate><creator>Ueda, Takafumi</creator><creator>Aozasa, Katsuyuki</creator><creator>Tsujimoto, Masahiko</creator><creator>Hamada, Hideki</creator><creator>Hayashi, Hideki</creator><creator>Ono, Keiro</creator><creator>Matsumoto, Keishi</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><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>7X8</scope></search><sort><creationdate>19881001</creationdate><title>Multivariate analysis for clinical prognostic factors in 163 patients with soft tissue sarcoma</title><author>Ueda, Takafumi ; Aozasa, Katsuyuki ; Tsujimoto, Masahiko ; Hamada, Hideki ; Hayashi, Hideki ; Ono, Keiro ; Matsumoto, Keishi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4983-7f63067d44b271185287e3025dee94194fde72b4c84feb108b496e5042bba583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Actuarial Analysis</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Prognosis</topic><topic>Sarcoma - pathology</topic><topic>Sarcoma - surgery</topic><topic>Sex Factors</topic><topic>Soft Tissue Neoplasms - pathology</topic><topic>Soft Tissue Neoplasms - surgery</topic><topic>Statistics as Topic</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ueda, Takafumi</creatorcontrib><creatorcontrib>Aozasa, Katsuyuki</creatorcontrib><creatorcontrib>Tsujimoto, Masahiko</creatorcontrib><creatorcontrib>Hamada, Hideki</creatorcontrib><creatorcontrib>Hayashi, Hideki</creatorcontrib><creatorcontrib>Ono, Keiro</creatorcontrib><creatorcontrib>Matsumoto, Keishi</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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ueda, Takafumi</au><au>Aozasa, Katsuyuki</au><au>Tsujimoto, Masahiko</au><au>Hamada, Hideki</au><au>Hayashi, Hideki</au><au>Ono, Keiro</au><au>Matsumoto, Keishi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multivariate analysis for clinical prognostic factors in 163 patients with soft tissue sarcoma</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1988-10-01</date><risdate>1988</risdate><volume>62</volume><issue>7</issue><spage>1444</spage><epage>1450</epage><pages>1444-1450</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>Clinical and histologic findings in 163 patients with localized soft tissue sarcoma (STS) in the extremities and trunk were reviewed. There were 91 male patients and 72 female patients ranging in age from 2 to 84 years (median, 46 years). The histologic status of the tumors was as follows: low grade, 29 cases; intermediate grade, 52 cases; and high grade, 82 cases. The primary tumors were treated by intralesional excision (two cases), marginal (88), wide local (52), or amputation (21). Subsequent adjuvant therapy was given to 61 patients; 17 had radiotherapy (RT), 27 had chemotherapy (CH), and 17 had combined RT and CH. The overall survival (P < 0.1) and disease‐free survival (P < 0.001) were better in the group that received multimodal treatment (radical surgery and adjuvant chemotherapy with or without radiotherapy) than in the group treated only by surgery. This suggests the favorable role of adjuvant therapy. The univariate and the Cox multivariate analysis for prognosis revealed that sex, tumor‐related symptoms, tumor size, tumor depth, and histologic grade were the significant factors. Among the treatment schemes, adjuvant chemotherapy was the only one that affected survival, especially for the intermediate‐grade tumors. Initial surgical treatment (marginal versus wide local excision) significantly contributed to the local control of the primary tumors.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>3416283</pmid><doi>10.1002/1097-0142(19881001)62:7<1444::AID-CNCR2820620733>3.0.CO;2-L</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actuarial Analysis Adolescent Adult Aged Aged, 80 and over Biological and medical sciences Child Child, Preschool Combined Modality Therapy Female Humans Infant Male Medical sciences Middle Aged Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Prognosis Sarcoma - pathology Sarcoma - surgery Sex Factors Soft Tissue Neoplasms - pathology Soft Tissue Neoplasms - surgery Statistics as Topic Tumors |
title | Multivariate analysis for clinical prognostic factors in 163 patients with soft tissue sarcoma |
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