Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12323
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dc.contributor.authorSegelov, Een
dc.contributor.authorChan, David Len
dc.contributor.authorShapiro, Jen
dc.contributor.authorPrice, Timothy Jen
dc.contributor.authorKarapetis, C Sen
dc.contributor.authorTebbutt, Niall Cen
dc.contributor.authorPavlakis, Nen
dc.date.accessioned2015-05-16T01:59:34Z
dc.date.available2015-05-16T01:59:34Z
dc.date.issued2014-07-29en
dc.identifier.citationBritish Journal of Cancer 2014; 111(6): 1122-31en
dc.identifier.govdoc25072258en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12323en
dc.description.abstractBiologic agents have achieved variable results in relapsed metastatic colorectal cancer (mCRC). Systematic meta-analysis was undertaken to determine the efficacy of biological therapy.Major databases were searched for randomised studies of mCRC after first-line treatment comparing (1) standard treatment plus biologic agent with standard treatment or (2) standard treatment with biologic agent with the same treatment with different biologic agent(s). Data were extracted on study design, participants, interventions and outcomes. Study quality was assessed using the MERGE criteria. Comparable data were pooled for meta-analysis.Twenty eligible studies with 8225 patients were identified. The use of any biologic therapy improved overall survival with hazard ratio (HR) 0.87 (95% confidence interval (CI) 0.82-0.91, P<0.00001), progression-free survival (PFS) with HR 0.71 (95% CI 0.67-0.74, P<0.0001) and overall response rate (ORR) with odds ratio (OR) 2.38 (95% CI 2.03-2.78, P<0.00001). Grade 3/4 toxicity was increased with OR 2.34. Considering by subgroups, EGFR inhibitors (EGFR-I) in the second-line setting and anti-angiogenic therapies (both in second-line and third-line and beyond settings) all improved overall survival, PFS and ORR. EGFR-I in third-line settings improved PFS and ORR but not OS.The use of biologic agents in mCRC after first-line treatment is associated with improved outcomes but increased toxicity.en
dc.language.isoenen
dc.subject.otherAngiogenesis Inhibitors.adverse effects.therapeutic useen
dc.subject.otherAntibodies, Monoclonal.adverse effects.therapeutic useen
dc.subject.otherBiological Therapy.adverse effectsen
dc.subject.otherColorectal Neoplasms.drug therapy.pathologyen
dc.subject.otherDisease-Free Survivalen
dc.subject.otherHumansen
dc.subject.otherRandomized Controlled Trials as Topicen
dc.subject.otherReceptor, Epidermal Growth Factor.antagonists & inhibitorsen
dc.subject.otherReceptors, Vascular Endothelial Growth Factor.antagonists & inhibitorsen
dc.subject.otherVascular Endothelial Growth Factor A.antagonists & inhibitorsen
dc.titleThe role of biological therapy in metastatic colorectal cancer after first-line treatment: a meta-analysis of randomised trials.en
dc.typeJournal Articleen
dc.identifier.journaltitleBritish Journal of Canceren
dc.identifier.affiliationAustin Health, VIC 3084, Australiaen
dc.identifier.affiliationFlinders University and Flinders Medical Centre, Flinders Centre for Innovation in Cancer, Bedford Park, SA, 5042, Australiaen
dc.identifier.affiliationThe Queen Elizabeth Hospital and University of Adelaide, Woodville South, SA 5011, Australiaen
dc.identifier.affiliationMonash University and Cabrini Hospital, Melbourne, VIC 3800, Australiaen
dc.identifier.affiliationRoyal North Shore Hospital, St Leonards, Sydney, NSW 2065, Australiaen
dc.identifier.affiliationSt Vincent's Clinical School, University of New South Wales, Sydney, NSW 2052, Australiaen
dc.identifier.doi10.1038/bjc.2014.404en
dc.description.pages1122-31en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/25072258en
dc.type.austinJournal Articleen
local.name.researcherTebbutt, Niall C
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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