Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/27666
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dc.contributor.authorGanju V.en
dc.contributor.authorDobrovic A.en
dc.contributor.authorTebbutt N.C.en
dc.contributor.authorParry M.M.en
dc.contributor.authorZannino D.en
dc.contributor.authorStrickland A.H.en
dc.contributor.authorVan Hazel G.A.en
dc.contributor.authorPavlakis N.en
dc.contributor.authorMellor D.en
dc.contributor.authorGebski V.J.en
dc.date.accessioned2021-05-14T09:19:00Zen
dc.date.available2021-05-14T09:19:00Zen
dc.date.copyright2013en
dc.date.created20130328en
dc.date.issued2013-03-28en
dc.identifier.citationBritish Journal of Cancer. 108 (4) (pp 771-774), 2013. Date of Publication: 05 Mar 2013.en
dc.identifier.issn0007-0920en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/27666en
dc.description.abstractBackground:Cetuximab can reverse chemotherapy resistance in colorectal cancer. This study evaluated the efficacy and safety of the combination of docetaxel and cetuximab as a second-line treatment in docetaxel-refractory oesophagogastric cancer. Method(s):Patients received docetaxel 30 mg m-2 on days 1 and 8, every 3 weeks and cetuximab 400 mg m-2 on day 1, then 250 mg m-2 weekly. Biomarker mutation analysis was performed. Result(s):A total of 38 patients were enrolled. Response rates were PR 6% (95% CI 2-19%), s.d. 43% (95% CI 28-59%). Main grade 3/4 toxicities were febrile neutropenia, anorexia, nausea, diarrhoea, stomatitis, and acneiform rash. Median progression-free and overall survival were 2.1 and 5.4 months, respectively. A landmark analysis showed a trend to improved survival times with increased grade of acneiform rash. No KRAS, BRAF or PIK3CA mutations were observed. Conclusion(s):Cetuximab and docetaxel achieve modest responses rates, but maintain comparable survival times to other salvage regimens with low rates of toxicity. © 2013 Cancer Research UK.en
dc.languageenen
dc.languageEnglishen
dc.publisherNature Publishing Group (Houndmills, Basingstoke, Hampshire RG21 6XS, United Kingdom)en
dc.titleDocetaxel plus cetuximab as second-line treatment for docetaxel-refractory oesophagogastric cancer: The AGITG ATTAX2 trial.en
dc.typeArticleen
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1038/bjc.2013.41en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid23412099 [http://www.ncbi.nlm.nih.gov/pubmed/?term=23412099]en
dc.identifier.source52444825en
dc.identifier.institution(Tebbutt) Department of Medical Oncology, Austin Health, PO Box 5555 Studley Road, Heidelberg Melbourne, VIC 3084, Australia (Parry, Zannino, Gebski) National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Locked Bag 77, Camperdown, Sydney NSW 1450, Australia (Strickland) Monash Medical Centre, 246 Clayton Road, Clayton, Melbourne, VIC 3168, Australia (Van Hazel) Sir Charles Gairdner Hospital, Hospital Avenue Nedlands, Perth, WA 6009, Australia (Pavlakis) Royal North Shore Hospital, Pacific Highway, St Leonards, Sydney, NSW 2064, Australia (Ganju) Frankston Hospital, PO Box 52, Frankston, Melbourne, VIC 3199, Australia (Mellor, Dobrovic) Peter MacCallum Cancer Centre, St Andrews Place, East Melbourne, Melbourne, VIC 3002, Australiaen
dc.description.addressN.C. Tebbutt, Department of Medical Oncology, Austin Health, PO Box 5555 Studley Road, Heidelberg Melbourne, VIC 3084, Australia. E-mail: niall.tebbutt@ludwig.edu.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2013 Elsevier B.V., All rights reserved.en
dc.subect.keywordsadvanced gastric cancer advanced oesophageal cancer cetuximab docetaxelen
dc.identifier.authoremailTebbutt N.C.; niall.tebbutt@ludwig.edu.auen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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