Long-term results of the co-operative German-Austrian-Swiss osteosarcoma study group's protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs
Background: In an effort to intensify osteosarcoma therapy, systemic ifosfamide was added pre- and postoperatively to an already aggressive three-drug regimen. In a subgroup of patients, loco-regional treatment intensification was attempted by using the intraarterial route to give cisplatin. Patient...
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Veröffentlicht in: | Annals of oncology 1998-08, Vol.9 (8), p.893-899 |
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creator | Fuchs, N. Bielack, S. S. Epler, D. Biding, P. Delling, G. Körholz, D. Graf, N. Heise, U. Jürgens, H. Kotz, R. Salzer-Kuntschik, M. Weinel, P. Werner, M. Winkler, K. |
description | Background: In an effort to intensify osteosarcoma therapy, systemic ifosfamide was added pre- and postoperatively to an already aggressive three-drug regimen. In a subgroup of patients, loco-regional treatment intensification was attempted by using the intraarterial route to give cisplatin. Patients and methods: Patients ≤ 40 years at diagnosis of a localised, de novo high-grade central extremity osteosarcoma were eligible for inclusion into study COSS-86 if registered within three weeks from biopsy. Doxorubicin, high-dose methotrexate, and cisplatin were given to all patients. Patients who fulfilled one or more of three defined high-risk criteria received early systemic treatment intensification by adding ifosfamide as the fourth agent. Preoperatively, these high-risk patients received cisplatin either intraarterially or intravenously. Results: 171 eligible patients were entered, of which 128 were stratified into the high-risk group. When all 171 were analysed by intention-to-treat, actuarial overall and event-free survival rates at ten years were 72% and 66%, respectively. No benefit of intraarterial cisplatin application was detected. Cumulative treatment toxicity was considerable. Conclusions: In a multicenter setting, intensive treatment of osteosarcoma according to protocol COSS-86 led to long-term disease-free survival for two thirds of patients. We saw no benefit of using the intraarterial route to administer cisplatin. |
doi_str_mv | 10.1023/A:1008391103132 |
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S. ; Epler, D. ; Biding, P. ; Delling, G. ; Körholz, D. ; Graf, N. ; Heise, U. ; Jürgens, H. ; Kotz, R. ; Salzer-Kuntschik, M. ; Weinel, P. ; Werner, M. ; Winkler, K.</creator><creatorcontrib>Fuchs, N. ; Bielack, S. S. ; Epler, D. ; Biding, P. ; Delling, G. ; Körholz, D. ; Graf, N. ; Heise, U. ; Jürgens, H. ; Kotz, R. ; Salzer-Kuntschik, M. ; Weinel, P. ; Werner, M. ; Winkler, K.</creatorcontrib><description>Background: In an effort to intensify osteosarcoma therapy, systemic ifosfamide was added pre- and postoperatively to an already aggressive three-drug regimen. In a subgroup of patients, loco-regional treatment intensification was attempted by using the intraarterial route to give cisplatin. Patients and methods: Patients ≤ 40 years at diagnosis of a localised, de novo high-grade central extremity osteosarcoma were eligible for inclusion into study COSS-86 if registered within three weeks from biopsy. Doxorubicin, high-dose methotrexate, and cisplatin were given to all patients. Patients who fulfilled one or more of three defined high-risk criteria received early systemic treatment intensification by adding ifosfamide as the fourth agent. Preoperatively, these high-risk patients received cisplatin either intraarterially or intravenously. Results: 171 eligible patients were entered, of which 128 were stratified into the high-risk group. When all 171 were analysed by intention-to-treat, actuarial overall and event-free survival rates at ten years were 72% and 66%, respectively. No benefit of intraarterial cisplatin application was detected. Cumulative treatment toxicity was considerable. Conclusions: In a multicenter setting, intensive treatment of osteosarcoma according to protocol COSS-86 led to long-term disease-free survival for two thirds of patients. We saw no benefit of using the intraarterial route to administer cisplatin.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1023/A:1008391103132</identifier><identifier>PMID: 9789613</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Arm - pathology ; Arm - surgery ; Biological and medical sciences ; Bone Neoplasms - drug therapy ; Bone Neoplasms - pathology ; Bone Neoplasms - surgery ; Chemotherapy ; Child, Preschool ; cisplatin ; Cisplatin - administration & dosage ; Doxorubicin - administration & dosage ; Female ; Humans ; ifosfamide ; Ifosfamide - administration & dosage ; Infusions, Intra-Arterial ; Infusions, Intravenous ; intraarterial therapy ; Leg - pathology ; Leg - surgery ; Male ; Medical sciences ; Methotrexate - administration & dosage ; Neoadjuvant Therapy ; osteosarcoma ; Osteosarcoma - drug therapy ; Osteosarcoma - pathology ; Osteosarcoma - surgery ; Pharmacology. Drug treatments ; Risk Factors ; Survival Analysis ; Treatment Outcome</subject><ispartof>Annals of oncology, 1998-08, Vol.9 (8), p.893-899</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-11376e452c6153ace9b67fd532686e79d38d0b9487a967efff8c8c1be74679453</citedby><cites>FETCH-LOGICAL-c466t-11376e452c6153ace9b67fd532686e79d38d0b9487a967efff8c8c1be74679453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1591659$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9789613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fuchs, N.</creatorcontrib><creatorcontrib>Bielack, S. S.</creatorcontrib><creatorcontrib>Epler, D.</creatorcontrib><creatorcontrib>Biding, P.</creatorcontrib><creatorcontrib>Delling, G.</creatorcontrib><creatorcontrib>Körholz, D.</creatorcontrib><creatorcontrib>Graf, N.</creatorcontrib><creatorcontrib>Heise, U.</creatorcontrib><creatorcontrib>Jürgens, H.</creatorcontrib><creatorcontrib>Kotz, R.</creatorcontrib><creatorcontrib>Salzer-Kuntschik, M.</creatorcontrib><creatorcontrib>Weinel, P.</creatorcontrib><creatorcontrib>Werner, M.</creatorcontrib><creatorcontrib>Winkler, K.</creatorcontrib><title>Long-term results of the co-operative German-Austrian-Swiss osteosarcoma study group's protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>Background: In an effort to intensify osteosarcoma therapy, systemic ifosfamide was added pre- and postoperatively to an already aggressive three-drug regimen. In a subgroup of patients, loco-regional treatment intensification was attempted by using the intraarterial route to give cisplatin. Patients and methods: Patients ≤ 40 years at diagnosis of a localised, de novo high-grade central extremity osteosarcoma were eligible for inclusion into study COSS-86 if registered within three weeks from biopsy. Doxorubicin, high-dose methotrexate, and cisplatin were given to all patients. Patients who fulfilled one or more of three defined high-risk criteria received early systemic treatment intensification by adding ifosfamide as the fourth agent. Preoperatively, these high-risk patients received cisplatin either intraarterially or intravenously. Results: 171 eligible patients were entered, of which 128 were stratified into the high-risk group. When all 171 were analysed by intention-to-treat, actuarial overall and event-free survival rates at ten years were 72% and 66%, respectively. No benefit of intraarterial cisplatin application was detected. Cumulative treatment toxicity was considerable. Conclusions: In a multicenter setting, intensive treatment of osteosarcoma according to protocol COSS-86 led to long-term disease-free survival for two thirds of patients. We saw no benefit of using the intraarterial route to administer cisplatin.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Arm - pathology</subject><subject>Arm - surgery</subject><subject>Biological and medical sciences</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - pathology</subject><subject>Bone Neoplasms - surgery</subject><subject>Chemotherapy</subject><subject>Child, Preschool</subject><subject>cisplatin</subject><subject>Cisplatin - administration & dosage</subject><subject>Doxorubicin - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>ifosfamide</subject><subject>Ifosfamide - administration & dosage</subject><subject>Infusions, Intra-Arterial</subject><subject>Infusions, Intravenous</subject><subject>intraarterial therapy</subject><subject>Leg - pathology</subject><subject>Leg - surgery</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methotrexate - administration & dosage</subject><subject>Neoadjuvant Therapy</subject><subject>osteosarcoma</subject><subject>Osteosarcoma - drug therapy</subject><subject>Osteosarcoma - pathology</subject><subject>Osteosarcoma - surgery</subject><subject>Pharmacology. Drug treatments</subject><subject>Risk Factors</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE-LEzEYh4Moa109exJyEDzFTSaTf95q1a5QXLEKxUvIZJLu6MxkSDJqP5jfz5SWlT0l8Hve5335AfCc4NcEV_Rq-YZgLKkiBFNCqwdgQRhXSOKaPAQLrCqKBKP1Y_AkpR8YY64qdQEulJCKE7oAfzdh3KPs4gCjS3OfEwwe5lsHbUBhctHk7peD6wKYES3nlGNXPtvfXSpkyi4kE20YDEx5bg9wH8M8vUpwiiEHG3q4utlukeRHazdmN6ajbiiLujbOe2hv3RDKumimAzRjC9Mc9y4eoA_xvv98Vt8NTXoKHnnTJ_fs_F6Cbx_ef11do83N-uNquUG25jwjQqjgrmaV5YRRY51quPAtoxWX3AnVUtniRtVSGMWF895LKy1pnKi5UDWjl-Dq5LUxpBSd11PsBhMPmmB97F8v9b3-y8SL08Q0N4Nr7_hz4SV_ec5Nsqb30Yy2S_-1TBHOVMHQCetKBX_uYhN_ai6oYPp6912vd-rd7u2nL_oz_Qd2-6Bh</recordid><startdate>19980801</startdate><enddate>19980801</enddate><creator>Fuchs, N.</creator><creator>Bielack, S. S.</creator><creator>Epler, D.</creator><creator>Biding, P.</creator><creator>Delling, G.</creator><creator>Körholz, D.</creator><creator>Graf, N.</creator><creator>Heise, U.</creator><creator>Jürgens, H.</creator><creator>Kotz, R.</creator><creator>Salzer-Kuntschik, M.</creator><creator>Weinel, P.</creator><creator>Werner, M.</creator><creator>Winkler, K.</creator><general>Oxford University Press</general><scope>BSCLL</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></search><sort><creationdate>19980801</creationdate><title>Long-term results of the co-operative German-Austrian-Swiss osteosarcoma study group's protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs</title><author>Fuchs, N. ; Bielack, S. S. ; Epler, D. ; Biding, P. ; Delling, G. ; Körholz, D. ; Graf, N. ; Heise, U. ; Jürgens, H. ; Kotz, R. ; Salzer-Kuntschik, M. ; Weinel, P. ; Werner, M. ; Winkler, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-11376e452c6153ace9b67fd532686e79d38d0b9487a967efff8c8c1be74679453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Arm - pathology</topic><topic>Arm - surgery</topic><topic>Biological and medical sciences</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Bone Neoplasms - pathology</topic><topic>Bone Neoplasms - surgery</topic><topic>Chemotherapy</topic><topic>Child, Preschool</topic><topic>cisplatin</topic><topic>Cisplatin - administration & dosage</topic><topic>Doxorubicin - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>ifosfamide</topic><topic>Ifosfamide - administration & dosage</topic><topic>Infusions, Intra-Arterial</topic><topic>Infusions, Intravenous</topic><topic>intraarterial therapy</topic><topic>Leg - pathology</topic><topic>Leg - surgery</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methotrexate - administration & dosage</topic><topic>Neoadjuvant Therapy</topic><topic>osteosarcoma</topic><topic>Osteosarcoma - drug therapy</topic><topic>Osteosarcoma - pathology</topic><topic>Osteosarcoma - surgery</topic><topic>Pharmacology. Drug treatments</topic><topic>Risk Factors</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fuchs, N.</creatorcontrib><creatorcontrib>Bielack, S. S.</creatorcontrib><creatorcontrib>Epler, D.</creatorcontrib><creatorcontrib>Biding, P.</creatorcontrib><creatorcontrib>Delling, G.</creatorcontrib><creatorcontrib>Körholz, D.</creatorcontrib><creatorcontrib>Graf, N.</creatorcontrib><creatorcontrib>Heise, U.</creatorcontrib><creatorcontrib>Jürgens, H.</creatorcontrib><creatorcontrib>Kotz, R.</creatorcontrib><creatorcontrib>Salzer-Kuntschik, M.</creatorcontrib><creatorcontrib>Weinel, P.</creatorcontrib><creatorcontrib>Werner, M.</creatorcontrib><creatorcontrib>Winkler, K.</creatorcontrib><collection>Istex</collection><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><jtitle>Annals of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fuchs, N.</au><au>Bielack, S. S.</au><au>Epler, D.</au><au>Biding, P.</au><au>Delling, G.</au><au>Körholz, D.</au><au>Graf, N.</au><au>Heise, U.</au><au>Jürgens, H.</au><au>Kotz, R.</au><au>Salzer-Kuntschik, M.</au><au>Weinel, P.</au><au>Werner, M.</au><au>Winkler, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term results of the co-operative German-Austrian-Swiss osteosarcoma study group's protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>1998-08-01</date><risdate>1998</risdate><volume>9</volume><issue>8</issue><spage>893</spage><epage>899</epage><pages>893-899</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>Background: In an effort to intensify osteosarcoma therapy, systemic ifosfamide was added pre- and postoperatively to an already aggressive three-drug regimen. In a subgroup of patients, loco-regional treatment intensification was attempted by using the intraarterial route to give cisplatin. Patients and methods: Patients ≤ 40 years at diagnosis of a localised, de novo high-grade central extremity osteosarcoma were eligible for inclusion into study COSS-86 if registered within three weeks from biopsy. Doxorubicin, high-dose methotrexate, and cisplatin were given to all patients. Patients who fulfilled one or more of three defined high-risk criteria received early systemic treatment intensification by adding ifosfamide as the fourth agent. Preoperatively, these high-risk patients received cisplatin either intraarterially or intravenously. Results: 171 eligible patients were entered, of which 128 were stratified into the high-risk group. When all 171 were analysed by intention-to-treat, actuarial overall and event-free survival rates at ten years were 72% and 66%, respectively. No benefit of intraarterial cisplatin application was detected. Cumulative treatment toxicity was considerable. Conclusions: In a multicenter setting, intensive treatment of osteosarcoma according to protocol COSS-86 led to long-term disease-free survival for two thirds of patients. We saw no benefit of using the intraarterial route to administer cisplatin.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>9789613</pmid><doi>10.1023/A:1008391103132</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Antineoplastic agents Antineoplastic Combined Chemotherapy Protocols - therapeutic use Arm - pathology Arm - surgery Biological and medical sciences Bone Neoplasms - drug therapy Bone Neoplasms - pathology Bone Neoplasms - surgery Chemotherapy Child, Preschool cisplatin Cisplatin - administration & dosage Doxorubicin - administration & dosage Female Humans ifosfamide Ifosfamide - administration & dosage Infusions, Intra-Arterial Infusions, Intravenous intraarterial therapy Leg - pathology Leg - surgery Male Medical sciences Methotrexate - administration & dosage Neoadjuvant Therapy osteosarcoma Osteosarcoma - drug therapy Osteosarcoma - pathology Osteosarcoma - surgery Pharmacology. Drug treatments Risk Factors Survival Analysis Treatment Outcome |
title | Long-term results of the co-operative German-Austrian-Swiss osteosarcoma study group's protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs |
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