Osteosarcoma: The Addition of Muramyl Tripeptide to Chemotherapy Improves Overall Survival—A Report From the Children's Oncology Group
To compare three-drug chemotherapy with cisplatin, doxorubicin, and methotrexate with four-drug chemotherapy with cisplatin, doxorubicin, methotrexate, and ifosfamide for the treatment of osteosarcoma. To determine whether the addition of muramyl tripeptide (MTP) to chemotherapy enhances event-free...
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Veröffentlicht in: | Journal of clinical oncology 2008-02, Vol.26 (4), p.633-638 |
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creator | MEYERS, Paul A SCHWARTZ, Cindy L KLEINERMAN, Eugenie LINK, Michael P NADEL, Helen NIEDER, Michael SIEGAL, Gene P WEINER, Michael A WELLS, Robert J WOMER, Richard B GRIER, Holcombe E KRAILO, Mark D HEALEY, John H BERNSTEIN, Mark L BETCHER, Donna FERGUSON, William S GEBHARDT, Mark C GOORIN, Alien M HARRIS, Michael |
description | To compare three-drug chemotherapy with cisplatin, doxorubicin, and methotrexate with four-drug chemotherapy with cisplatin, doxorubicin, methotrexate, and ifosfamide for the treatment of osteosarcoma. To determine whether the addition of muramyl tripeptide (MTP) to chemotherapy enhances event-free survival (EFS) and overall survival in newly diagnosed patients with osteosarcoma.
Six hundred sixty-two patients with osteosarcoma without clinically detectable metastatic disease and whose disease was considered resectable received one of four prospectively randomized treatments. All patients received identical cumulative doses of cisplatin, doxorubicin, and methotrexate and underwent definitive surgical resection of primary tumor. Patients were randomly assigned to receive or not to receive ifosfamide and/or MTP in a 2 x 2 factorial design. The primary end points for analysis were EFS and overall survival.
In the current analysis, there was no evidence of interaction, and we were able to examine each intervention separately. The chemotherapy regimens resulted in similar EFS and overall survival. There was a trend toward better EFS with the addition of MTP (P = .08). The addition of MTP to chemotherapy improved 6-year overall survival from 70% to 78% (P = .03). The hazard ratio for overall survival with the addition of MTP was 0.71 (95% CI, 0.52 to 0.96).
The addition of ifosfamide to cisplatin, doxorubicin, and methotrexate did not enhance EFS or overall survival for patients with osteosarcoma. The addition of MTP to chemotherapy resulted in a statistically significant improvement in overall survival and a trend toward better EFS. |
doi_str_mv | 10.1200/JCO.2008.14.0095 |
format | Article |
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Six hundred sixty-two patients with osteosarcoma without clinically detectable metastatic disease and whose disease was considered resectable received one of four prospectively randomized treatments. All patients received identical cumulative doses of cisplatin, doxorubicin, and methotrexate and underwent definitive surgical resection of primary tumor. Patients were randomly assigned to receive or not to receive ifosfamide and/or MTP in a 2 x 2 factorial design. The primary end points for analysis were EFS and overall survival.
In the current analysis, there was no evidence of interaction, and we were able to examine each intervention separately. The chemotherapy regimens resulted in similar EFS and overall survival. There was a trend toward better EFS with the addition of MTP (P = .08). The addition of MTP to chemotherapy improved 6-year overall survival from 70% to 78% (P = .03). The hazard ratio for overall survival with the addition of MTP was 0.71 (95% CI, 0.52 to 0.96).
The addition of ifosfamide to cisplatin, doxorubicin, and methotrexate did not enhance EFS or overall survival for patients with osteosarcoma. The addition of MTP to chemotherapy resulted in a statistically significant improvement in overall survival and a trend toward better EFS.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2008.14.0095</identifier><identifier>PMID: 18235123</identifier><language>eng</language><publisher>Baltimore, MD: American Society of Clinical Oncology</publisher><subject>Adolescent ; Adult ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Bone Neoplasms - drug therapy ; Bone Neoplasms - mortality ; Child ; Child, Preschool ; Cisplatin - administration & dosage ; Disease-Free Survival ; Diseases of the osteoarticular system ; Doxorubicin - administration & dosage ; Female ; Humans ; Ifosfamide - administration & dosage ; Infant ; Lung Neoplasms - secondary ; Male ; Medical sciences ; Methotrexate - administration & dosage ; Neoplasm Recurrence, Local ; Osteosarcoma - drug therapy ; Osteosarcoma - mortality ; Osteosarcoma - secondary ; Survival Rate ; Tumors ; Tumors of striated muscle and skeleton</subject><ispartof>Journal of clinical oncology, 2008-02, Vol.26 (4), p.633-638</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-683b4cc7914d01925493c64ac39be65aa4d19687822247b30d3e51b71b7163923</citedby><cites>FETCH-LOGICAL-c512t-683b4cc7914d01925493c64ac39be65aa4d19687822247b30d3e51b71b7163923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3716,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20050453$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18235123$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MEYERS, Paul A</creatorcontrib><creatorcontrib>SCHWARTZ, Cindy L</creatorcontrib><creatorcontrib>KLEINERMAN, Eugenie</creatorcontrib><creatorcontrib>LINK, Michael P</creatorcontrib><creatorcontrib>NADEL, Helen</creatorcontrib><creatorcontrib>NIEDER, Michael</creatorcontrib><creatorcontrib>SIEGAL, Gene P</creatorcontrib><creatorcontrib>WEINER, Michael A</creatorcontrib><creatorcontrib>WELLS, Robert J</creatorcontrib><creatorcontrib>WOMER, Richard B</creatorcontrib><creatorcontrib>GRIER, Holcombe E</creatorcontrib><creatorcontrib>KRAILO, Mark D</creatorcontrib><creatorcontrib>HEALEY, John H</creatorcontrib><creatorcontrib>BERNSTEIN, Mark L</creatorcontrib><creatorcontrib>BETCHER, Donna</creatorcontrib><creatorcontrib>FERGUSON, William S</creatorcontrib><creatorcontrib>GEBHARDT, Mark C</creatorcontrib><creatorcontrib>GOORIN, Alien M</creatorcontrib><creatorcontrib>HARRIS, Michael</creatorcontrib><creatorcontrib>Children's Oncology Group</creatorcontrib><title>Osteosarcoma: The Addition of Muramyl Tripeptide to Chemotherapy Improves Overall Survival—A Report From the Children's Oncology Group</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>To compare three-drug chemotherapy with cisplatin, doxorubicin, and methotrexate with four-drug chemotherapy with cisplatin, doxorubicin, methotrexate, and ifosfamide for the treatment of osteosarcoma. To determine whether the addition of muramyl tripeptide (MTP) to chemotherapy enhances event-free survival (EFS) and overall survival in newly diagnosed patients with osteosarcoma.
Six hundred sixty-two patients with osteosarcoma without clinically detectable metastatic disease and whose disease was considered resectable received one of four prospectively randomized treatments. All patients received identical cumulative doses of cisplatin, doxorubicin, and methotrexate and underwent definitive surgical resection of primary tumor. Patients were randomly assigned to receive or not to receive ifosfamide and/or MTP in a 2 x 2 factorial design. The primary end points for analysis were EFS and overall survival.
In the current analysis, there was no evidence of interaction, and we were able to examine each intervention separately. The chemotherapy regimens resulted in similar EFS and overall survival. There was a trend toward better EFS with the addition of MTP (P = .08). The addition of MTP to chemotherapy improved 6-year overall survival from 70% to 78% (P = .03). The hazard ratio for overall survival with the addition of MTP was 0.71 (95% CI, 0.52 to 0.96).
The addition of ifosfamide to cisplatin, doxorubicin, and methotrexate did not enhance EFS or overall survival for patients with osteosarcoma. The addition of MTP to chemotherapy resulted in a statistically significant improvement in overall survival and a trend toward better EFS.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - mortality</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cisplatin - administration & dosage</subject><subject>Disease-Free Survival</subject><subject>Diseases of the osteoarticular system</subject><subject>Doxorubicin - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Ifosfamide - administration & dosage</subject><subject>Infant</subject><subject>Lung Neoplasms - secondary</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methotrexate - administration & dosage</subject><subject>Neoplasm Recurrence, Local</subject><subject>Osteosarcoma - drug therapy</subject><subject>Osteosarcoma - mortality</subject><subject>Osteosarcoma - secondary</subject><subject>Survival Rate</subject><subject>Tumors</subject><subject>Tumors of striated muscle and skeleton</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkM2KFDEURoMoTju6dyXZqKtq81upctc0zjgy0qAtuAup1O2pDKlKmVS19M6lDzBPOE9immlUuHDhcr6Py0HoJSVLygh592m9WeZdLalYElLLR2hBJVOFUlI-RguiOCtoxb-foWcp3RJCRcXlU3RGK8YlZXyBfm_SBCGZaENv3uNtB3jVtm5yYcBhhz_P0fQHj7fRjTBOrgU8BbzuoA9TB9GMB3zVjzHsIeHNPh-8x1_nuHd74-9_3a3wFxhDnPBFDD3OiRx1vo0wvM38YIMPNwd8GcM8PkdPdsYneHHa5-jbxYft-mNxvbm8Wq-uC5sfnoqy4o2wVtVUtITWTIqa21IYy-sGSmmMaGldVqpijAnVcNJykLRRxyl5zfg5evPQm7_-MUOadO-SBe_NAGFOWhEmOaMqg-QBtDGkFGGnx-h6Ew-aEn20r7N9fbSvqdBH-zny6tQ9Nz20_wIn3Rl4fQJMssbvohmsS3-5XCaJkP9xnbvpfroIOvVZba5l-tYGVmqhS875H8Gvmw0</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>MEYERS, Paul A</creator><creator>SCHWARTZ, Cindy L</creator><creator>KLEINERMAN, Eugenie</creator><creator>LINK, Michael P</creator><creator>NADEL, Helen</creator><creator>NIEDER, Michael</creator><creator>SIEGAL, Gene P</creator><creator>WEINER, Michael A</creator><creator>WELLS, Robert J</creator><creator>WOMER, Richard B</creator><creator>GRIER, Holcombe E</creator><creator>KRAILO, Mark D</creator><creator>HEALEY, John H</creator><creator>BERNSTEIN, Mark L</creator><creator>BETCHER, Donna</creator><creator>FERGUSON, William S</creator><creator>GEBHARDT, Mark C</creator><creator>GOORIN, Alien M</creator><creator>HARRIS, Michael</creator><general>American Society of Clinical Oncology</general><general>Lippincott Williams & Wilkins</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>20080201</creationdate><title>Osteosarcoma: The Addition of Muramyl Tripeptide to Chemotherapy Improves Overall Survival—A Report From the Children's Oncology Group</title><author>MEYERS, Paul A ; SCHWARTZ, Cindy L ; KLEINERMAN, Eugenie ; LINK, Michael P ; NADEL, Helen ; NIEDER, Michael ; SIEGAL, Gene P ; WEINER, Michael A ; WELLS, Robert J ; WOMER, Richard B ; GRIER, Holcombe E ; KRAILO, Mark D ; HEALEY, John H ; BERNSTEIN, Mark L ; BETCHER, Donna ; FERGUSON, William S ; GEBHARDT, Mark C ; GOORIN, Alien M ; HARRIS, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-683b4cc7914d01925493c64ac39be65aa4d19687822247b30d3e51b71b7163923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Bone Neoplasms - mortality</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cisplatin - administration & dosage</topic><topic>Disease-Free Survival</topic><topic>Diseases of the osteoarticular system</topic><topic>Doxorubicin - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Ifosfamide - administration & dosage</topic><topic>Infant</topic><topic>Lung Neoplasms - secondary</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methotrexate - administration & dosage</topic><topic>Neoplasm Recurrence, Local</topic><topic>Osteosarcoma - drug therapy</topic><topic>Osteosarcoma - mortality</topic><topic>Osteosarcoma - secondary</topic><topic>Survival Rate</topic><topic>Tumors</topic><topic>Tumors of striated muscle and skeleton</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MEYERS, Paul A</creatorcontrib><creatorcontrib>SCHWARTZ, Cindy L</creatorcontrib><creatorcontrib>KLEINERMAN, Eugenie</creatorcontrib><creatorcontrib>LINK, Michael P</creatorcontrib><creatorcontrib>NADEL, Helen</creatorcontrib><creatorcontrib>NIEDER, Michael</creatorcontrib><creatorcontrib>SIEGAL, Gene P</creatorcontrib><creatorcontrib>WEINER, Michael A</creatorcontrib><creatorcontrib>WELLS, Robert J</creatorcontrib><creatorcontrib>WOMER, Richard B</creatorcontrib><creatorcontrib>GRIER, Holcombe E</creatorcontrib><creatorcontrib>KRAILO, Mark D</creatorcontrib><creatorcontrib>HEALEY, John H</creatorcontrib><creatorcontrib>BERNSTEIN, Mark L</creatorcontrib><creatorcontrib>BETCHER, Donna</creatorcontrib><creatorcontrib>FERGUSON, William S</creatorcontrib><creatorcontrib>GEBHARDT, Mark C</creatorcontrib><creatorcontrib>GOORIN, Alien M</creatorcontrib><creatorcontrib>HARRIS, Michael</creatorcontrib><creatorcontrib>Children's Oncology Group</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>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MEYERS, Paul A</au><au>SCHWARTZ, Cindy L</au><au>KLEINERMAN, Eugenie</au><au>LINK, Michael P</au><au>NADEL, Helen</au><au>NIEDER, Michael</au><au>SIEGAL, Gene P</au><au>WEINER, Michael A</au><au>WELLS, Robert J</au><au>WOMER, Richard B</au><au>GRIER, Holcombe E</au><au>KRAILO, Mark D</au><au>HEALEY, John H</au><au>BERNSTEIN, Mark L</au><au>BETCHER, Donna</au><au>FERGUSON, William S</au><au>GEBHARDT, Mark C</au><au>GOORIN, Alien M</au><au>HARRIS, Michael</au><aucorp>Children's Oncology Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteosarcoma: The Addition of Muramyl Tripeptide to Chemotherapy Improves Overall Survival—A Report From the Children's Oncology Group</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>26</volume><issue>4</issue><spage>633</spage><epage>638</epage><pages>633-638</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>To compare three-drug chemotherapy with cisplatin, doxorubicin, and methotrexate with four-drug chemotherapy with cisplatin, doxorubicin, methotrexate, and ifosfamide for the treatment of osteosarcoma. To determine whether the addition of muramyl tripeptide (MTP) to chemotherapy enhances event-free survival (EFS) and overall survival in newly diagnosed patients with osteosarcoma.
Six hundred sixty-two patients with osteosarcoma without clinically detectable metastatic disease and whose disease was considered resectable received one of four prospectively randomized treatments. All patients received identical cumulative doses of cisplatin, doxorubicin, and methotrexate and underwent definitive surgical resection of primary tumor. Patients were randomly assigned to receive or not to receive ifosfamide and/or MTP in a 2 x 2 factorial design. The primary end points for analysis were EFS and overall survival.
In the current analysis, there was no evidence of interaction, and we were able to examine each intervention separately. The chemotherapy regimens resulted in similar EFS and overall survival. There was a trend toward better EFS with the addition of MTP (P = .08). The addition of MTP to chemotherapy improved 6-year overall survival from 70% to 78% (P = .03). The hazard ratio for overall survival with the addition of MTP was 0.71 (95% CI, 0.52 to 0.96).
The addition of ifosfamide to cisplatin, doxorubicin, and methotrexate did not enhance EFS or overall survival for patients with osteosarcoma. The addition of MTP to chemotherapy resulted in a statistically significant improvement in overall survival and a trend toward better EFS.</abstract><cop>Baltimore, MD</cop><pub>American Society of Clinical Oncology</pub><pmid>18235123</pmid><doi>10.1200/JCO.2008.14.0095</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Adolescent Adult Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Bone Neoplasms - drug therapy Bone Neoplasms - mortality Child Child, Preschool Cisplatin - administration & dosage Disease-Free Survival Diseases of the osteoarticular system Doxorubicin - administration & dosage Female Humans Ifosfamide - administration & dosage Infant Lung Neoplasms - secondary Male Medical sciences Methotrexate - administration & dosage Neoplasm Recurrence, Local Osteosarcoma - drug therapy Osteosarcoma - mortality Osteosarcoma - secondary Survival Rate Tumors Tumors of striated muscle and skeleton |
title | Osteosarcoma: The Addition of Muramyl Tripeptide to Chemotherapy Improves Overall Survival—A Report From the Children's Oncology Group |
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