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https://ahro.austin.org.au/austinjspui/handle/1/12323
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Segelov, E | en |
dc.contributor.author | Chan, David L | en |
dc.contributor.author | Shapiro, J | en |
dc.contributor.author | Price, Timothy J | en |
dc.contributor.author | Karapetis, C S | en |
dc.contributor.author | Tebbutt, Niall C | en |
dc.contributor.author | Pavlakis, N | en |
dc.date.accessioned | 2015-05-16T01:59:34Z | |
dc.date.available | 2015-05-16T01:59:34Z | |
dc.date.issued | 2014-07-29 | en |
dc.identifier.citation | British Journal of Cancer 2014; 111(6): 1122-31 | en |
dc.identifier.govdoc | 25072258 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/12323 | en |
dc.description.abstract | Biologic 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.iso | en | en |
dc.subject.other | Angiogenesis Inhibitors.adverse effects.therapeutic use | en |
dc.subject.other | Antibodies, Monoclonal.adverse effects.therapeutic use | en |
dc.subject.other | Biological Therapy.adverse effects | en |
dc.subject.other | Colorectal Neoplasms.drug therapy.pathology | en |
dc.subject.other | Disease-Free Survival | en |
dc.subject.other | Humans | en |
dc.subject.other | Randomized Controlled Trials as Topic | en |
dc.subject.other | Receptor, Epidermal Growth Factor.antagonists & inhibitors | en |
dc.subject.other | Receptors, Vascular Endothelial Growth Factor.antagonists & inhibitors | en |
dc.subject.other | Vascular Endothelial Growth Factor A.antagonists & inhibitors | en |
dc.title | The role of biological therapy in metastatic colorectal cancer after first-line treatment: a meta-analysis of randomised trials. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | British Journal of Cancer | en |
dc.identifier.affiliation | Austin Health, VIC 3084, Australia | en |
dc.identifier.affiliation | Flinders University and Flinders Medical Centre, Flinders Centre for Innovation in Cancer, Bedford Park, SA, 5042, Australia | en |
dc.identifier.affiliation | The Queen Elizabeth Hospital and University of Adelaide, Woodville South, SA 5011, Australia | en |
dc.identifier.affiliation | Monash University and Cabrini Hospital, Melbourne, VIC 3800, Australia | en |
dc.identifier.affiliation | Royal North Shore Hospital, St Leonards, Sydney, NSW 2065, Australia | en |
dc.identifier.affiliation | St Vincent's Clinical School, University of New South Wales, Sydney, NSW 2052, Australia | en |
dc.identifier.doi | 10.1038/bjc.2014.404 | en |
dc.description.pages | 1122-31 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/25072258 | en |
dc.type.austin | Journal Article | en |
local.name.researcher | Tebbutt, Niall C | |
item.openairetype | Journal Article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | Medical Oncology | - |
crisitem.author.dept | Olivia Newton-John Cancer Wellness and Research Centre | - |
Appears in Collections: | Journal articles |
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