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Conservative surgery and postoperative radiotherapy in 300 adults with soft‐tissue sarcomas
From January 1963 through December 1977, 300 adults with soft‐tissue sarcomas were treated by a conservative surgical excision and postoperative radiotherapy. The absolute two‐ and five‐year disease‐free survival rates are 74% (222/300) and 61.3% (103/168), respectively. The five‐year survival rate...
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Published in: | Cancer 1981-05, Vol.47 (10), p.2391-2397 |
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description | From January 1963 through December 1977, 300 adults with soft‐tissue sarcomas were treated by a conservative surgical excision and postoperative radiotherapy. The absolute two‐ and five‐year disease‐free survival rates are 74% (222/300) and 61.3% (103/168), respectively. The five‐year survival rate varies with: (1) anatomic site, e.g., 69.4% (75/108) for extremity lesions vs. 33% (5/15) for abdominal lesions; (2) histopathologic diagnosis, e.g., 86.4% (19/22) for fibrosarcoma vs. 50% (15/30) for neurofibrosarcoma; and (3) stage of the lesion. The overall local recurrence rate was 22.3% (67/300) and 27% (81/300) of the patients developed distant metastases. The incidence of lymph node metastases as an initial site of spread was only 2.7% (8/300); therefore, elective treatment of the regional lymphatics is not indicated. The 6.5% incidence of significant complications in extremities is low and might be further diminished by careful treatment planning. The combination of conservative surgery and postoperative radiation therapy maintains a functional limb in 84.5% (169/200) of patients with extremity lesions. This rate is comparable to the five‐year survival rate attained with radical surgery. |
doi_str_mv | 10.1002/1097-0142(19810515)47:10<2391::AID-CNCR2820471012>3.0.CO;2-B |
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Thomas</creator><creatorcontrib>Lindberg, Robert D. ; Martin, Richard G. ; Romsdahl, Marvin M. ; Barkley, H. Thomas</creatorcontrib><description>From January 1963 through December 1977, 300 adults with soft‐tissue sarcomas were treated by a conservative surgical excision and postoperative radiotherapy. The absolute two‐ and five‐year disease‐free survival rates are 74% (222/300) and 61.3% (103/168), respectively. The five‐year survival rate varies with: (1) anatomic site, e.g., 69.4% (75/108) for extremity lesions vs. 33% (5/15) for abdominal lesions; (2) histopathologic diagnosis, e.g., 86.4% (19/22) for fibrosarcoma vs. 50% (15/30) for neurofibrosarcoma; and (3) stage of the lesion. The overall local recurrence rate was 22.3% (67/300) and 27% (81/300) of the patients developed distant metastases. The incidence of lymph node metastases as an initial site of spread was only 2.7% (8/300); therefore, elective treatment of the regional lymphatics is not indicated. The 6.5% incidence of significant complications in extremities is low and might be further diminished by careful treatment planning. The combination of conservative surgery and postoperative radiation therapy maintains a functional limb in 84.5% (169/200) of patients with extremity lesions. This rate is comparable to the five‐year survival rate attained with radical surgery.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19810515)47:10<2391::AID-CNCR2820471012>3.0.CO;2-B</identifier><identifier>PMID: 7272893</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Abdomen ; Adolescent ; Extremities ; Fibrosarcoma - surgery ; Humans ; Neoplasm Metastasis ; Neoplasm Recurrence, Local ; Neoplasm Staging ; Neurofibroma - surgery ; Postoperative Complications ; Prognosis ; Retrospective Studies ; Sarcoma - pathology ; Sarcoma - radiotherapy ; Sarcoma - surgery ; Soft Tissue Neoplasms - pathology ; Soft Tissue Neoplasms - radiotherapy ; Soft Tissue Neoplasms - surgery</subject><ispartof>Cancer, 1981-05, Vol.47 (10), p.2391-2397</ispartof><rights>Copyright © 1981 American Cancer Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4722-319f6521e856c5f2edf43c0ae7685843244ec55b6a7c6a73adf888c0b3672d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7272893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lindberg, Robert D.</creatorcontrib><creatorcontrib>Martin, Richard G.</creatorcontrib><creatorcontrib>Romsdahl, Marvin M.</creatorcontrib><creatorcontrib>Barkley, H. Thomas</creatorcontrib><title>Conservative surgery and postoperative radiotherapy in 300 adults with soft‐tissue sarcomas</title><title>Cancer</title><addtitle>Cancer</addtitle><description>From January 1963 through December 1977, 300 adults with soft‐tissue sarcomas were treated by a conservative surgical excision and postoperative radiotherapy. The absolute two‐ and five‐year disease‐free survival rates are 74% (222/300) and 61.3% (103/168), respectively. The five‐year survival rate varies with: (1) anatomic site, e.g., 69.4% (75/108) for extremity lesions vs. 33% (5/15) for abdominal lesions; (2) histopathologic diagnosis, e.g., 86.4% (19/22) for fibrosarcoma vs. 50% (15/30) for neurofibrosarcoma; and (3) stage of the lesion. The overall local recurrence rate was 22.3% (67/300) and 27% (81/300) of the patients developed distant metastases. The incidence of lymph node metastases as an initial site of spread was only 2.7% (8/300); therefore, elective treatment of the regional lymphatics is not indicated. The 6.5% incidence of significant complications in extremities is low and might be further diminished by careful treatment planning. The combination of conservative surgery and postoperative radiation therapy maintains a functional limb in 84.5% (169/200) of patients with extremity lesions. This rate is comparable to the five‐year survival rate attained with radical surgery.</description><subject>Abdomen</subject><subject>Adolescent</subject><subject>Extremities</subject><subject>Fibrosarcoma - surgery</subject><subject>Humans</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasm Recurrence, Local</subject><subject>Neoplasm Staging</subject><subject>Neurofibroma - surgery</subject><subject>Postoperative Complications</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Sarcoma - pathology</subject><subject>Sarcoma - radiotherapy</subject><subject>Sarcoma - surgery</subject><subject>Soft Tissue Neoplasms - pathology</subject><subject>Soft Tissue Neoplasms - radiotherapy</subject><subject>Soft Tissue Neoplasms - surgery</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNqVkM9q3DAQh0VoSbebPELBp9IevB39s-RtKCRO2wRCF0oOPbQMWllOXLwrV7IT9tZH6DP2SWqz20ByCOQghuEb_Ub6CDmlMKMA7B2FXKVABXtDc01BUvlWqDmFI8ZzOp8fn5-mxZfiK9MMhKJA2Qc-g1mxeM_Skz0yubv-jEwAQKdS8G8vyMsYfw6tYpLvk33FFNM5n5AfhV9HF25MV9-4JPbhyoVNYtZl0vrY-daFLQmmrH13PbTtJqnXCQdITNk3XUxu6-46ib7q_v7-09Ux9kOOCdavTDwgzyvTRHe4q1Ny-enjZXGWXiw-nxfHF6kVirGU07zKJKNOy8zKirmyEtyCcSrTUgvOhHBWymVmlB0ON2Wltbaw5JliJeVT8nob2wb_q3exw1UdrWsas3a-j6h4RnM5_HdKvm8HbfAxBldhG-qVCRukgKN8HO3haA__y0ehRjrKRxzk4335yBGwWCDDkyH-1e4d_XLlyrvwne2BX235bd24zRN3P7r6AeH_AJXfo70</recordid><startdate>19810515</startdate><enddate>19810515</enddate><creator>Lindberg, Robert D.</creator><creator>Martin, Richard G.</creator><creator>Romsdahl, Marvin M.</creator><creator>Barkley, H. 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Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4722-319f6521e856c5f2edf43c0ae7685843244ec55b6a7c6a73adf888c0b3672d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Abdomen</topic><topic>Adolescent</topic><topic>Extremities</topic><topic>Fibrosarcoma - surgery</topic><topic>Humans</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasm Recurrence, Local</topic><topic>Neoplasm Staging</topic><topic>Neurofibroma - surgery</topic><topic>Postoperative Complications</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Sarcoma - pathology</topic><topic>Sarcoma - radiotherapy</topic><topic>Sarcoma - surgery</topic><topic>Soft Tissue Neoplasms - pathology</topic><topic>Soft Tissue Neoplasms - radiotherapy</topic><topic>Soft Tissue Neoplasms - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lindberg, Robert D.</creatorcontrib><creatorcontrib>Martin, Richard G.</creatorcontrib><creatorcontrib>Romsdahl, Marvin M.</creatorcontrib><creatorcontrib>Barkley, H. Thomas</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>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lindberg, Robert D.</au><au>Martin, Richard G.</au><au>Romsdahl, Marvin M.</au><au>Barkley, H. Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conservative surgery and postoperative radiotherapy in 300 adults with soft‐tissue sarcomas</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1981-05-15</date><risdate>1981</risdate><volume>47</volume><issue>10</issue><spage>2391</spage><epage>2397</epage><pages>2391-2397</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>From January 1963 through December 1977, 300 adults with soft‐tissue sarcomas were treated by a conservative surgical excision and postoperative radiotherapy. The absolute two‐ and five‐year disease‐free survival rates are 74% (222/300) and 61.3% (103/168), respectively. The five‐year survival rate varies with: (1) anatomic site, e.g., 69.4% (75/108) for extremity lesions vs. 33% (5/15) for abdominal lesions; (2) histopathologic diagnosis, e.g., 86.4% (19/22) for fibrosarcoma vs. 50% (15/30) for neurofibrosarcoma; and (3) stage of the lesion. The overall local recurrence rate was 22.3% (67/300) and 27% (81/300) of the patients developed distant metastases. The incidence of lymph node metastases as an initial site of spread was only 2.7% (8/300); therefore, elective treatment of the regional lymphatics is not indicated. The 6.5% incidence of significant complications in extremities is low and might be further diminished by careful treatment planning. The combination of conservative surgery and postoperative radiation therapy maintains a functional limb in 84.5% (169/200) of patients with extremity lesions. This rate is comparable to the five‐year survival rate attained with radical surgery.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7272893</pmid><doi>10.1002/1097-0142(19810515)47:10<2391::AID-CNCR2820471012>3.0.CO;2-B</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Adolescent Extremities Fibrosarcoma - surgery Humans Neoplasm Metastasis Neoplasm Recurrence, Local Neoplasm Staging Neurofibroma - surgery Postoperative Complications Prognosis Retrospective Studies Sarcoma - pathology Sarcoma - radiotherapy Sarcoma - surgery Soft Tissue Neoplasms - pathology Soft Tissue Neoplasms - radiotherapy Soft Tissue Neoplasms - surgery |
title | Conservative surgery and postoperative radiotherapy in 300 adults with soft‐tissue sarcomas |
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