Results of the COSS-77 and COSS-80 studies on adjuvant chemotherapy in osteosarcoma of the extremities

In the first study, COSS-77, 100 patients with OS were treated for 12 months according to a CT-protocol consisting of high-dose methotrexate (HD-MTX), adriblastine (ADR) and cyclophosphamide (CP). At 40 months the expected continuous disease-free survival (CDFS) rate of the 71 evaluable patients was...

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Veröffentlicht in:Klinische Pädiatrie 1985-05, Vol.197 (3), p.233
Hauptverfasser: Purfürst, C, Beron, G, Torggler, S, Kotz, R, Salzer-Kuntschik, M, Winkler, K
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container_start_page 233
container_title Klinische Pädiatrie
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creator Purfürst, C
Beron, G
Torggler, S
Kotz, R
Salzer-Kuntschik, M
Winkler, K
description In the first study, COSS-77, 100 patients with OS were treated for 12 months according to a CT-protocol consisting of high-dose methotrexate (HD-MTX), adriblastine (ADR) and cyclophosphamide (CP). At 40 months the expected continuous disease-free survival (CDFS) rate of the 71 evaluable patients was 55%. After exclusion of local recurrences (n = 2) and fatal chemotherapy toxicities (n = 0) a reduced group of 69 patients remained and the expected CDFS rate at 40 months became 56%. In the second study, COSS-80, the MTX dose was doubled. Two groups were randomly selected, one of which received cisplatinum (CPL) and the other the triple drug combination bleomycin + CP + dactinomycin (BCD) in addition to MTX and ADR, both groups being treated for 8 months. Furthermore some randomly selected patients received fibroblaste-interferon (IF). The expected CDFS rate at 40 months of the 115 evaluable COSS-80 patients was 67%. 106 patients remained in a reduced group defined as above (4 local recurrences and 5 CT toxicities) in which the expected CDFS rate at 40 months was 73%. This is significantly better (p less than 0.05) than the results obtained from the COSS-77 group. No differences were found between the CPL and BCD arms of the COSS-80 group or between the arms receiving or not receiving IF. A significant increase in the CDFS rate for young (less than 12 years) and male patients over that in COSS-77 was observed in COSS-80, probably due to the increased MTX dose.
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At 40 months the expected continuous disease-free survival (CDFS) rate of the 71 evaluable patients was 55%. After exclusion of local recurrences (n = 2) and fatal chemotherapy toxicities (n = 0) a reduced group of 69 patients remained and the expected CDFS rate at 40 months became 56%. In the second study, COSS-80, the MTX dose was doubled. Two groups were randomly selected, one of which received cisplatinum (CPL) and the other the triple drug combination bleomycin + CP + dactinomycin (BCD) in addition to MTX and ADR, both groups being treated for 8 months. Furthermore some randomly selected patients received fibroblaste-interferon (IF). The expected CDFS rate at 40 months of the 115 evaluable COSS-80 patients was 67%. 106 patients remained in a reduced group defined as above (4 local recurrences and 5 CT toxicities) in which the expected CDFS rate at 40 months was 73%. This is significantly better (p less than 0.05) than the results obtained from the COSS-77 group. No differences were found between the CPL and BCD arms of the COSS-80 group or between the arms receiving or not receiving IF. A significant increase in the CDFS rate for young (less than 12 years) and male patients over that in COSS-77 was observed in COSS-80, probably due to the increased MTX dose.</description><identifier>ISSN: 0300-8630</identifier><identifier>PMID: 2409325</identifier><language>ger</language><publisher>Germany</publisher><subject><![CDATA[Amputation ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bleomycin - administration & dosage ; Bone Neoplasms - drug therapy ; Child ; Cisplatin - administration & dosage ; Clinical Trials as Topic ; Combined Modality Therapy ; Cyclophosphamide - administration & dosage ; Dactinomycin - administration & dosage ; Doxorubicin - administration & dosage ; Extremities ; Female ; Humans ; Lung Neoplasms - secondary ; Male ; Methotrexate - administration & dosage ; Neoplasm Recurrence, Local - etiology ; Osteosarcoma - drug therapy ; Osteosarcoma - secondary]]></subject><ispartof>Klinische Pädiatrie, 1985-05, Vol.197 (3), p.233</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2409325$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Purfürst, C</creatorcontrib><creatorcontrib>Beron, G</creatorcontrib><creatorcontrib>Torggler, S</creatorcontrib><creatorcontrib>Kotz, R</creatorcontrib><creatorcontrib>Salzer-Kuntschik, M</creatorcontrib><creatorcontrib>Winkler, K</creatorcontrib><title>Results of the COSS-77 and COSS-80 studies on adjuvant chemotherapy in osteosarcoma of the extremities</title><title>Klinische Pädiatrie</title><addtitle>Klin Padiatr</addtitle><description>In the first study, COSS-77, 100 patients with OS were treated for 12 months according to a CT-protocol consisting of high-dose methotrexate (HD-MTX), adriblastine (ADR) and cyclophosphamide (CP). At 40 months the expected continuous disease-free survival (CDFS) rate of the 71 evaluable patients was 55%. After exclusion of local recurrences (n = 2) and fatal chemotherapy toxicities (n = 0) a reduced group of 69 patients remained and the expected CDFS rate at 40 months became 56%. In the second study, COSS-80, the MTX dose was doubled. Two groups were randomly selected, one of which received cisplatinum (CPL) and the other the triple drug combination bleomycin + CP + dactinomycin (BCD) in addition to MTX and ADR, both groups being treated for 8 months. Furthermore some randomly selected patients received fibroblaste-interferon (IF). The expected CDFS rate at 40 months of the 115 evaluable COSS-80 patients was 67%. 106 patients remained in a reduced group defined as above (4 local recurrences and 5 CT toxicities) in which the expected CDFS rate at 40 months was 73%. This is significantly better (p less than 0.05) than the results obtained from the COSS-77 group. No differences were found between the CPL and BCD arms of the COSS-80 group or between the arms receiving or not receiving IF. A significant increase in the CDFS rate for young (less than 12 years) and male patients over that in COSS-77 was observed in COSS-80, probably due to the increased MTX dose.</description><subject>Amputation</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bleomycin - administration &amp; dosage</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Child</subject><subject>Cisplatin - administration &amp; dosage</subject><subject>Clinical Trials as Topic</subject><subject>Combined Modality Therapy</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Dactinomycin - administration &amp; dosage</subject><subject>Doxorubicin - administration &amp; dosage</subject><subject>Extremities</subject><subject>Female</subject><subject>Humans</subject><subject>Lung Neoplasms - secondary</subject><subject>Male</subject><subject>Methotrexate - administration &amp; dosage</subject><subject>Neoplasm Recurrence, Local - etiology</subject><subject>Osteosarcoma - drug therapy</subject><subject>Osteosarcoma - secondary</subject><issn>0300-8630</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j8tqwzAURLVoSdM0nxDQDxiuJOvhZTF9QSDQZB8k-4o4xJaR5NL8fQ1JVzMwcwbmgSxBABRGCXgizymdAVhZQbUgC15CJbhcEv-NabrkRIOn-YS03u33hdbUDu3NG6ApT22Hc2Wgtj1PP3bItDlhH2Yg2vFKu4GGlDEkG5vQ2_8t_M0R-y7P7At59PaScH3XFTm8vx3qz2K7-_iqX7fFKIUsGEMmrOPOA-fKNBy4Vhwaj5UyErVBUJaBN3yOnBOcIWiFomwdE1IqsSKb2-w4uR7b4xi73sbr8X5X_AEMG08N</recordid><startdate>198505</startdate><enddate>198505</enddate><creator>Purfürst, C</creator><creator>Beron, G</creator><creator>Torggler, S</creator><creator>Kotz, R</creator><creator>Salzer-Kuntschik, M</creator><creator>Winkler, K</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>198505</creationdate><title>Results of the COSS-77 and COSS-80 studies on adjuvant chemotherapy in osteosarcoma of the extremities</title><author>Purfürst, C ; Beron, G ; Torggler, S ; Kotz, R ; Salzer-Kuntschik, M ; Winkler, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p535-11e13ab2bf02268c2027620cfe9685e78e06a10f82c20bb321e076e34db135563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>ger</language><creationdate>1985</creationdate><topic>Amputation</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Bleomycin - administration &amp; dosage</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Child</topic><topic>Cisplatin - administration &amp; dosage</topic><topic>Clinical Trials as Topic</topic><topic>Combined Modality Therapy</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>Dactinomycin - administration &amp; dosage</topic><topic>Doxorubicin - administration &amp; dosage</topic><topic>Extremities</topic><topic>Female</topic><topic>Humans</topic><topic>Lung Neoplasms - secondary</topic><topic>Male</topic><topic>Methotrexate - administration &amp; dosage</topic><topic>Neoplasm Recurrence, Local - etiology</topic><topic>Osteosarcoma - drug therapy</topic><topic>Osteosarcoma - secondary</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Purfürst, C</creatorcontrib><creatorcontrib>Beron, G</creatorcontrib><creatorcontrib>Torggler, S</creatorcontrib><creatorcontrib>Kotz, R</creatorcontrib><creatorcontrib>Salzer-Kuntschik, M</creatorcontrib><creatorcontrib>Winkler, K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Klinische Pädiatrie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Purfürst, C</au><au>Beron, G</au><au>Torggler, S</au><au>Kotz, R</au><au>Salzer-Kuntschik, M</au><au>Winkler, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Results of the COSS-77 and COSS-80 studies on adjuvant chemotherapy in osteosarcoma of the extremities</atitle><jtitle>Klinische Pädiatrie</jtitle><addtitle>Klin Padiatr</addtitle><date>1985-05</date><risdate>1985</risdate><volume>197</volume><issue>3</issue><spage>233</spage><pages>233-</pages><issn>0300-8630</issn><abstract>In the first study, COSS-77, 100 patients with OS were treated for 12 months according to a CT-protocol consisting of high-dose methotrexate (HD-MTX), adriblastine (ADR) and cyclophosphamide (CP). At 40 months the expected continuous disease-free survival (CDFS) rate of the 71 evaluable patients was 55%. After exclusion of local recurrences (n = 2) and fatal chemotherapy toxicities (n = 0) a reduced group of 69 patients remained and the expected CDFS rate at 40 months became 56%. In the second study, COSS-80, the MTX dose was doubled. Two groups were randomly selected, one of which received cisplatinum (CPL) and the other the triple drug combination bleomycin + CP + dactinomycin (BCD) in addition to MTX and ADR, both groups being treated for 8 months. Furthermore some randomly selected patients received fibroblaste-interferon (IF). The expected CDFS rate at 40 months of the 115 evaluable COSS-80 patients was 67%. 106 patients remained in a reduced group defined as above (4 local recurrences and 5 CT toxicities) in which the expected CDFS rate at 40 months was 73%. This is significantly better (p less than 0.05) than the results obtained from the COSS-77 group. No differences were found between the CPL and BCD arms of the COSS-80 group or between the arms receiving or not receiving IF. A significant increase in the CDFS rate for young (less than 12 years) and male patients over that in COSS-77 was observed in COSS-80, probably due to the increased MTX dose.</abstract><cop>Germany</cop><pmid>2409325</pmid></addata></record>
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source MEDLINE; Thieme Connect Journals
subjects Amputation
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Bleomycin - administration & dosage
Bone Neoplasms - drug therapy
Child
Cisplatin - administration & dosage
Clinical Trials as Topic
Combined Modality Therapy
Cyclophosphamide - administration & dosage
Dactinomycin - administration & dosage
Doxorubicin - administration & dosage
Extremities
Female
Humans
Lung Neoplasms - secondary
Male
Methotrexate - administration & dosage
Neoplasm Recurrence, Local - etiology
Osteosarcoma - drug therapy
Osteosarcoma - secondary
title Results of the COSS-77 and COSS-80 studies on adjuvant chemotherapy in osteosarcoma of the extremities
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