Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials
Background: Several randomised trials have compared interferon-α with control as adjuvant therapy for high-risk malignant melanoma. The results of the individual trials have been either inconclusive or even apparently conflicting. To assess all the available evidence we performed a meta-analysis of...
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Veröffentlicht in: | Cancer treatment reviews 2003-08, Vol.29 (4), p.241-252 |
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description | Background: Several randomised trials have compared interferon-α with control as adjuvant therapy for high-risk malignant melanoma. The results of the individual trials have been either inconclusive or even apparently conflicting. To assess all the available evidence we performed a meta-analysis of these trials.
Methods: Standard methods for quantitative meta-analysis based on published data were used. Endpoints evaluated were recurrence-free survival and overall survival. A subgroup analysis by dose of interferon-α was performed.
Findings: Twelve trials, comprising 14 comparisons of interferon-α with control, with results available were identified. Recurrence-free survival was improved with interferon-α: hazard ratio 0.83, 95% confidence interval 0.77 to 0.90,
p=0.000003. The benefit on overall survival was less clear (0.93, 0.85 to 1.02,
p=0.1) and the confidence interval is compatible both with no benefit and with a moderate, but clinically worthwhile, benefit. There was some evidence of a dose response relationship with a significant trend for the benefit of interferon-α to increase with increasing dose for recurrence-free survival (test for trend:
p=0.02) but not for overall survival (trend:
p=0.8).
Interpretation: This meta-analysis provides the most reliable synthesis of the data currently available. Adjuvant interferon-α produces clear reductions in recurrence of high-risk melanoma, with some evidence of an effect of dose of interferon-α, but it is unclear whether this translates into a worthwhile survival benefit or not. Additional and more mature data are needed to resolve these issues and an individual patient data meta-analysis should be performed. |
doi_str_mv | 10.1016/S0305-7372(03)00074-4 |
format | Article |
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Methods: Standard methods for quantitative meta-analysis based on published data were used. Endpoints evaluated were recurrence-free survival and overall survival. A subgroup analysis by dose of interferon-α was performed.
Findings: Twelve trials, comprising 14 comparisons of interferon-α with control, with results available were identified. Recurrence-free survival was improved with interferon-α: hazard ratio 0.83, 95% confidence interval 0.77 to 0.90,
p=0.000003. The benefit on overall survival was less clear (0.93, 0.85 to 1.02,
p=0.1) and the confidence interval is compatible both with no benefit and with a moderate, but clinically worthwhile, benefit. There was some evidence of a dose response relationship with a significant trend for the benefit of interferon-α to increase with increasing dose for recurrence-free survival (test for trend:
p=0.02) but not for overall survival (trend:
p=0.8).
Interpretation: This meta-analysis provides the most reliable synthesis of the data currently available. Adjuvant interferon-α produces clear reductions in recurrence of high-risk melanoma, with some evidence of an effect of dose of interferon-α, but it is unclear whether this translates into a worthwhile survival benefit or not. Additional and more mature data are needed to resolve these issues and an individual patient data meta-analysis should be performed.</description><identifier>ISSN: 0305-7372</identifier><identifier>EISSN: 1532-1967</identifier><identifier>DOI: 10.1016/S0305-7372(03)00074-4</identifier><identifier>PMID: 12927565</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - therapeutic use ; Chemotherapy, Adjuvant ; Disease-Free Survival ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Humans ; Interferon-alpha - administration & dosage ; Interferon-alpha - therapeutic use ; interferon-α ; melanoma ; Melanoma - drug therapy ; Melanoma - surgery ; Meta-analysis ; randomised controlled trials ; Randomized Controlled Trials as Topic ; Risk Assessment ; Skin Neoplasms - drug therapy ; Skin Neoplasms - surgery ; Survival Analysis</subject><ispartof>Cancer treatment reviews, 2003-08, Vol.29 (4), p.241-252</ispartof><rights>2003 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c361t-93542720c65d14204a8882e7da6bdb19074f3a859548bdc350d7049bc27181673</citedby><cites>FETCH-LOGICAL-c361t-93542720c65d14204a8882e7da6bdb19074f3a859548bdc350d7049bc27181673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0305-7372(03)00074-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12927565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wheatley, Keith</creatorcontrib><creatorcontrib>Ives, Natalie</creatorcontrib><creatorcontrib>Hancock, Barry</creatorcontrib><creatorcontrib>Gore, Martin</creatorcontrib><creatorcontrib>Eggermont, Alexander</creatorcontrib><creatorcontrib>Suciu, Stefan</creatorcontrib><title>Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials</title><title>Cancer treatment reviews</title><addtitle>Cancer Treat Rev</addtitle><description>Background: Several randomised trials have compared interferon-α with control as adjuvant therapy for high-risk malignant melanoma. The results of the individual trials have been either inconclusive or even apparently conflicting. To assess all the available evidence we performed a meta-analysis of these trials.
Methods: Standard methods for quantitative meta-analysis based on published data were used. Endpoints evaluated were recurrence-free survival and overall survival. A subgroup analysis by dose of interferon-α was performed.
Findings: Twelve trials, comprising 14 comparisons of interferon-α with control, with results available were identified. Recurrence-free survival was improved with interferon-α: hazard ratio 0.83, 95% confidence interval 0.77 to 0.90,
p=0.000003. The benefit on overall survival was less clear (0.93, 0.85 to 1.02,
p=0.1) and the confidence interval is compatible both with no benefit and with a moderate, but clinically worthwhile, benefit. There was some evidence of a dose response relationship with a significant trend for the benefit of interferon-α to increase with increasing dose for recurrence-free survival (test for trend:
p=0.02) but not for overall survival (trend:
p=0.8).
Interpretation: This meta-analysis provides the most reliable synthesis of the data currently available. Adjuvant interferon-α produces clear reductions in recurrence of high-risk melanoma, with some evidence of an effect of dose of interferon-α, but it is unclear whether this translates into a worthwhile survival benefit or not. Additional and more mature data are needed to resolve these issues and an individual patient data meta-analysis should be performed.</description><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Chemotherapy, Adjuvant</subject><subject>Disease-Free Survival</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Humans</subject><subject>Interferon-alpha - administration & dosage</subject><subject>Interferon-alpha - therapeutic use</subject><subject>interferon-α</subject><subject>melanoma</subject><subject>Melanoma - drug therapy</subject><subject>Melanoma - surgery</subject><subject>Meta-analysis</subject><subject>randomised controlled trials</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Risk Assessment</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - surgery</subject><subject>Survival Analysis</subject><issn>0305-7372</issn><issn>1532-1967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtuFDEQRS1ERCaBTwB5hZKFwY-23b2KovCUImUBrC23XU07dLeD7ZloPis_wjfFkxnBklVtTtWtexB6zeg7Rpl6_40KKokWmp9RcU4p1Q1pnqEVk4IT1in9HK3-IsfoJOfbCnVCdS_QMeMd11LJFdp-iJCx9bfrjV0KDkuBNECKC_nzgIeY8Bh-jiSF_AvPMNklzhbfpbgJHrDF9zGV8X4ME-AeFhhCucCXFSyW2MVO2xwyjgMuI-BkFx_nkMHjkoKd8kt0NNQBrw7zFP349PH71RdyffP569XlNXFCsUI6IRuuOXVKetZw2ti2bTlob1Xve9bV3oOwrexk0_beCUm9pk3XO65Zy5QWp-jt_m59-_cacjH1CwdTLQNxnY0WslVcNhWUe9ClmHOCwdylMNu0NYyanXPz5NzshBoqzJNzs9t7cwhY9zP4f1sHyRW42ANQa24CJJNdgMWBDwlcMT6G_0Q8ArtMkfw</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Wheatley, Keith</creator><creator>Ives, Natalie</creator><creator>Hancock, Barry</creator><creator>Gore, Martin</creator><creator>Eggermont, Alexander</creator><creator>Suciu, Stefan</creator><general>Elsevier Ltd</general><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>20030801</creationdate><title>Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials</title><author>Wheatley, Keith ; Ives, Natalie ; Hancock, Barry ; Gore, Martin ; Eggermont, Alexander ; Suciu, Stefan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c361t-93542720c65d14204a8882e7da6bdb19074f3a859548bdc350d7049bc27181673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Chemotherapy, Adjuvant</topic><topic>Disease-Free Survival</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Humans</topic><topic>Interferon-alpha - administration & dosage</topic><topic>Interferon-alpha - therapeutic use</topic><topic>interferon-α</topic><topic>melanoma</topic><topic>Melanoma - drug therapy</topic><topic>Melanoma - surgery</topic><topic>Meta-analysis</topic><topic>randomised controlled trials</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Risk Assessment</topic><topic>Skin Neoplasms - drug therapy</topic><topic>Skin Neoplasms - surgery</topic><topic>Survival Analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wheatley, Keith</creatorcontrib><creatorcontrib>Ives, Natalie</creatorcontrib><creatorcontrib>Hancock, Barry</creatorcontrib><creatorcontrib>Gore, Martin</creatorcontrib><creatorcontrib>Eggermont, Alexander</creatorcontrib><creatorcontrib>Suciu, Stefan</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 treatment reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wheatley, Keith</au><au>Ives, Natalie</au><au>Hancock, Barry</au><au>Gore, Martin</au><au>Eggermont, Alexander</au><au>Suciu, Stefan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials</atitle><jtitle>Cancer treatment reviews</jtitle><addtitle>Cancer Treat Rev</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>29</volume><issue>4</issue><spage>241</spage><epage>252</epage><pages>241-252</pages><issn>0305-7372</issn><eissn>1532-1967</eissn><abstract>Background: Several randomised trials have compared interferon-α with control as adjuvant therapy for high-risk malignant melanoma. The results of the individual trials have been either inconclusive or even apparently conflicting. To assess all the available evidence we performed a meta-analysis of these trials.
Methods: Standard methods for quantitative meta-analysis based on published data were used. Endpoints evaluated were recurrence-free survival and overall survival. A subgroup analysis by dose of interferon-α was performed.
Findings: Twelve trials, comprising 14 comparisons of interferon-α with control, with results available were identified. Recurrence-free survival was improved with interferon-α: hazard ratio 0.83, 95% confidence interval 0.77 to 0.90,
p=0.000003. The benefit on overall survival was less clear (0.93, 0.85 to 1.02,
p=0.1) and the confidence interval is compatible both with no benefit and with a moderate, but clinically worthwhile, benefit. There was some evidence of a dose response relationship with a significant trend for the benefit of interferon-α to increase with increasing dose for recurrence-free survival (test for trend:
p=0.02) but not for overall survival (trend:
p=0.8).
Interpretation: This meta-analysis provides the most reliable synthesis of the data currently available. Adjuvant interferon-α produces clear reductions in recurrence of high-risk melanoma, with some evidence of an effect of dose of interferon-α, but it is unclear whether this translates into a worthwhile survival benefit or not. Additional and more mature data are needed to resolve these issues and an individual patient data meta-analysis should be performed.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>12927565</pmid><doi>10.1016/S0305-7372(03)00074-4</doi><tpages>12</tpages></addata></record> |
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subjects | Antineoplastic Agents - administration & dosage Antineoplastic Agents - therapeutic use Chemotherapy, Adjuvant Disease-Free Survival Dose-Response Relationship, Drug Drug Administration Schedule Humans Interferon-alpha - administration & dosage Interferon-alpha - therapeutic use interferon-α melanoma Melanoma - drug therapy Melanoma - surgery Meta-analysis randomised controlled trials Randomized Controlled Trials as Topic Risk Assessment Skin Neoplasms - drug therapy Skin Neoplasms - surgery Survival Analysis |
title | Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials |
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