Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35769
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dc.contributor.authorAthauda A.en
dc.contributor.authorSegelov E.en
dc.contributor.authorAli Z.en
dc.contributor.authorChau I.en
dc.date.accessioned2021-05-14T12:06:08Zen
dc.date.available2021-05-14T12:06:08Zen
dc.date.copyright2019en
dc.date.created20190103en
dc.date.issued2019-01-03en
dc.identifier.citationCancer Treatment Reviews. 73 (pp 31-40), 2019. Date of Publication: February 2019.en
dc.identifier.issn0305-7372en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/35769en
dc.description.abstractGastrointestinal (GI) malignancies comprise a diverse group of cancers with varying aetiology, clinical course, management and prognosis. Advances over the last decade in molecular diagnostics in colorectal cancer (CRC) have helped to improve our understanding of the underlying complex mechanisms in the development and progression of this highly heterogenous disease. Large scale integrative analysis has identified molecularly distinct subgroups of CRC with differing clinical behaviour. It was hoped that these discoveries would fuel the development of novel drug targets and new treatments to shift the management of advanced CRC from an empirical strategy to a biomarker driven approach based on underlying molecular characteristics. However, biomarkers in current clinical practice remain limited in CRC. Gastric cancer (GC) has also been slow to benefit from biomarker discovery and development and the successful utilisation of targeted therapies, with the exception of trastuzumab in HER2 positive cancers. More recently, molecular analysis of GC has also identified distinct subgroups within these cancers with differing behaviour and therapeutic targets. In addition, our deeper understanding of the underlying molecular biology of GI cancers has led to the consideration of alterations above and beyond gene mutations. The clonal, stromal and immune characteristics of GI malignancies are increasingly recognised as important in therapeutic targeting. The challenge remains to apply the data generated through molecular exploration into clinical practice in order to provide personalised treatment to each individual patient.Copyright © 2018 Elsevier Ltden
dc.languageEnglishen
dc.languageenen
dc.publisherW.B. Saunders Ltden
dc.relation.ispartofCancer Treatment Reviewsen
dc.titleIntegrative molecular analysis of colorectal cancer and gastric cancer: What have we learnt?.en
dc.typeReviewen
dc.identifier.affiliationOncology-
dc.type.studyortrialReview article (e.g. literature review, narrative review)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.ctrv.2018.12.004en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid30597479 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30597479]en
dc.identifier.source2001412110en
dc.identifier.institution(Athauda, Ali, Chau) Gastrointestinal and Lymphoma Unit, The Royal Marsden Hospital, Downs Road, Sutton, Surrey SM2 5PT, United Kingdom (Segelov) Monash Health and Monash University, Level 7, MHTP Building, Monash Health 246 Clayton Road, Victoria 3168, Australiaen
dc.description.addressI. Chau, Gastrointestinal and Lymphoma Unit, The Royal Marsden Hospital, Downs Road, Sutton, Surrey SM2 5PT, United Kingdom. E-mail: ian.chau@rmh.nhs.uken
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.subect.keywordsBiomarkers Gastrointestinal cancers Gene expression profiles Molecular subclassificationen
dc.identifier.authoremailAthauda A.; avani.athauda@rmh.nhs.uk Ali Z.; zohra.ali@rmh.nhs.uk Chau I.; ian.chau@rmh.nhs.uk Segelov E.; eva.segelov@monash.eduen
dc.description.grantOrganization: *Institute of Cancer Research* Organization No: 501100000027 Country: Canada Organization: *Royal Marsden NHS Foundation Trust* Organization No: 100012139 Country: United Kingdomen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeReview-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptOncology-
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