If there is no overall survival benefit in metastatic breast cancer: Does it imply lack of efficacy? Taxanes as an example
Abstract In recent years, new drugs have shown activity in metastatic breast cancer, but not always resulting in an overall survival benefit. This has led to discussions if such drugs, mainly expensive drugs, should be reimbursed especially when also not leading to improvement in quality of life. Fo...
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Veröffentlicht in: | Cancer treatment reviews 2013-04, Vol.39 (2), p.189-198 |
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description | Abstract In recent years, new drugs have shown activity in metastatic breast cancer, but not always resulting in an overall survival benefit. This has led to discussions if such drugs, mainly expensive drugs, should be reimbursed especially when also not leading to improvement in quality of life. For that reason, we decided to systematically review taxane-based chemotherapy studies in early and metastatic breast cancer, to assess which factors may have caused the differential outcome. Taxanes did not improve survival in metastatic breast cancer trials, whereas they did so in early breast cancer trials. We questioned if the differential outcome of taxanes in metastatic breast cancer might be caused by the chosen comparator and study design. We noticed that in the majority of metastatic breast cancer studies taxanes were used as a substitute for other active cytotoxic drugs, mainly cyclophosphamide, whereas in early breast cancer studies taxanes were generally delivered in addition to a standard regimen. We conclude from our analyses that use of taxanes instead of other active drugs explains the lack of overall survival benefit in metastatic breast cancer trials. Further, our results suggest that cyclophosphamide is an important drug in the treatment of breast cancer, being as effective as optimally dosed taxanes and anthracyclines. By studying the different study designs and comparators in both settings, we were able to demonstrate their impact on efficacy endpoints. We conclude, therefore, that re-assessment of studies of drugs both assessed in metastatic and early breast cancer provides a new tool for improved understanding. |
doi_str_mv | 10.1016/j.ctrv.2012.04.005 |
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Taxanes as an example</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Vriens, Birgit E.P.J ; Lobbezoo, Dorien J.A ; de Hoon, Joep P.J ; Veeck, Jürgen ; Voogd, Adri C ; Tjan-Heijnen, Vivianne C.G</creator><creatorcontrib>Vriens, Birgit E.P.J ; Lobbezoo, Dorien J.A ; de Hoon, Joep P.J ; Veeck, Jürgen ; Voogd, Adri C ; Tjan-Heijnen, Vivianne C.G</creatorcontrib><description>Abstract In recent years, new drugs have shown activity in metastatic breast cancer, but not always resulting in an overall survival benefit. This has led to discussions if such drugs, mainly expensive drugs, should be reimbursed especially when also not leading to improvement in quality of life. For that reason, we decided to systematically review taxane-based chemotherapy studies in early and metastatic breast cancer, to assess which factors may have caused the differential outcome. Taxanes did not improve survival in metastatic breast cancer trials, whereas they did so in early breast cancer trials. We questioned if the differential outcome of taxanes in metastatic breast cancer might be caused by the chosen comparator and study design. We noticed that in the majority of metastatic breast cancer studies taxanes were used as a substitute for other active cytotoxic drugs, mainly cyclophosphamide, whereas in early breast cancer studies taxanes were generally delivered in addition to a standard regimen. We conclude from our analyses that use of taxanes instead of other active drugs explains the lack of overall survival benefit in metastatic breast cancer trials. Further, our results suggest that cyclophosphamide is an important drug in the treatment of breast cancer, being as effective as optimally dosed taxanes and anthracyclines. By studying the different study designs and comparators in both settings, we were able to demonstrate their impact on efficacy endpoints. We conclude, therefore, that re-assessment of studies of drugs both assessed in metastatic and early breast cancer provides a new tool for improved understanding.</description><identifier>ISSN: 0305-7372</identifier><identifier>EISSN: 1532-1967</identifier><identifier>DOI: 10.1016/j.ctrv.2012.04.005</identifier><identifier>PMID: 22658318</identifier><identifier>CODEN: CTREDJ</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Antineoplastic agents ; Biological and medical sciences ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - mortality ; Breast Neoplasms - pathology ; Chemotherapy ; Clinical Trials as Topic ; Docetaxel ; Female ; Gynecology. Andrology. Obstetrics ; Hematology, Oncology and Palliative Medicine ; Humans ; Mammary gland diseases ; Medical sciences ; Neoplasm Metastasis - drug therapy ; Paclitaxel ; Pharmacology. Drug treatments ; Survival Analysis ; Taxanes ; Taxoids - therapeutic use ; Treatment Outcome ; Tumors</subject><ispartof>Cancer treatment reviews, 2013-04, Vol.39 (2), p.189-198</ispartof><rights>Elsevier Ltd</rights><rights>2012 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-98160e99fed32fa6a87deb17d243f680c63d853ac36038b8ba8e76d747ab65e03</citedby><cites>FETCH-LOGICAL-c441t-98160e99fed32fa6a87deb17d243f680c63d853ac36038b8ba8e76d747ab65e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ctrv.2012.04.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27096542$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22658318$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vriens, Birgit E.P.J</creatorcontrib><creatorcontrib>Lobbezoo, Dorien J.A</creatorcontrib><creatorcontrib>de Hoon, Joep P.J</creatorcontrib><creatorcontrib>Veeck, Jürgen</creatorcontrib><creatorcontrib>Voogd, Adri C</creatorcontrib><creatorcontrib>Tjan-Heijnen, Vivianne C.G</creatorcontrib><title>If there is no overall survival benefit in metastatic breast cancer: Does it imply lack of efficacy? Taxanes as an example</title><title>Cancer treatment reviews</title><addtitle>Cancer Treat Rev</addtitle><description>Abstract In recent years, new drugs have shown activity in metastatic breast cancer, but not always resulting in an overall survival benefit. This has led to discussions if such drugs, mainly expensive drugs, should be reimbursed especially when also not leading to improvement in quality of life. For that reason, we decided to systematically review taxane-based chemotherapy studies in early and metastatic breast cancer, to assess which factors may have caused the differential outcome. Taxanes did not improve survival in metastatic breast cancer trials, whereas they did so in early breast cancer trials. We questioned if the differential outcome of taxanes in metastatic breast cancer might be caused by the chosen comparator and study design. We noticed that in the majority of metastatic breast cancer studies taxanes were used as a substitute for other active cytotoxic drugs, mainly cyclophosphamide, whereas in early breast cancer studies taxanes were generally delivered in addition to a standard regimen. We conclude from our analyses that use of taxanes instead of other active drugs explains the lack of overall survival benefit in metastatic breast cancer trials. Further, our results suggest that cyclophosphamide is an important drug in the treatment of breast cancer, being as effective as optimally dosed taxanes and anthracyclines. By studying the different study designs and comparators in both settings, we were able to demonstrate their impact on efficacy endpoints. We conclude, therefore, that re-assessment of studies of drugs both assessed in metastatic and early breast cancer provides a new tool for improved understanding.</description><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - mortality</subject><subject>Breast Neoplasms - pathology</subject><subject>Chemotherapy</subject><subject>Clinical Trials as Topic</subject><subject>Docetaxel</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Neoplasm Metastasis - drug therapy</subject><subject>Paclitaxel</subject><subject>Pharmacology. 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Taxanes as an example</title><author>Vriens, Birgit E.P.J ; Lobbezoo, Dorien J.A ; de Hoon, Joep P.J ; Veeck, Jürgen ; Voogd, Adri C ; Tjan-Heijnen, Vivianne C.G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-98160e99fed32fa6a87deb17d243f680c63d853ac36038b8ba8e76d747ab65e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - mortality</topic><topic>Breast Neoplasms - pathology</topic><topic>Chemotherapy</topic><topic>Clinical Trials as Topic</topic><topic>Docetaxel</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Neoplasm Metastasis - drug therapy</topic><topic>Paclitaxel</topic><topic>Pharmacology. 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Taxanes as an example</atitle><jtitle>Cancer treatment reviews</jtitle><addtitle>Cancer Treat Rev</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>39</volume><issue>2</issue><spage>189</spage><epage>198</epage><pages>189-198</pages><issn>0305-7372</issn><eissn>1532-1967</eissn><coden>CTREDJ</coden><abstract>Abstract In recent years, new drugs have shown activity in metastatic breast cancer, but not always resulting in an overall survival benefit. This has led to discussions if such drugs, mainly expensive drugs, should be reimbursed especially when also not leading to improvement in quality of life. For that reason, we decided to systematically review taxane-based chemotherapy studies in early and metastatic breast cancer, to assess which factors may have caused the differential outcome. Taxanes did not improve survival in metastatic breast cancer trials, whereas they did so in early breast cancer trials. We questioned if the differential outcome of taxanes in metastatic breast cancer might be caused by the chosen comparator and study design. We noticed that in the majority of metastatic breast cancer studies taxanes were used as a substitute for other active cytotoxic drugs, mainly cyclophosphamide, whereas in early breast cancer studies taxanes were generally delivered in addition to a standard regimen. We conclude from our analyses that use of taxanes instead of other active drugs explains the lack of overall survival benefit in metastatic breast cancer trials. Further, our results suggest that cyclophosphamide is an important drug in the treatment of breast cancer, being as effective as optimally dosed taxanes and anthracyclines. By studying the different study designs and comparators in both settings, we were able to demonstrate their impact on efficacy endpoints. 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subjects | Antineoplastic agents Biological and medical sciences Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - mortality Breast Neoplasms - pathology Chemotherapy Clinical Trials as Topic Docetaxel Female Gynecology. Andrology. Obstetrics Hematology, Oncology and Palliative Medicine Humans Mammary gland diseases Medical sciences Neoplasm Metastasis - drug therapy Paclitaxel Pharmacology. Drug treatments Survival Analysis Taxanes Taxoids - therapeutic use Treatment Outcome Tumors |
title | If there is no overall survival benefit in metastatic breast cancer: Does it imply lack of efficacy? Taxanes as an example |
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