Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34833
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dc.contributor.authorAllan, Zexi-
dc.contributor.authorLiu, David Shi Hao-
dc.contributor.authorLee, Margaret M-
dc.contributor.authorTie, Jeanne-
dc.contributor.authorClemons, Nicholas J-
dc.date.accessioned2024-01-11T02:02:24Z-
dc.date.available2024-01-11T02:02:24Z-
dc.date.issued2024-01-04-
dc.identifier.citationClinical Chemistry 2024-01-04; 70(1)en_US
dc.identifier.issn1530-8561-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34833-
dc.description.abstractThere is accumulating evidence supporting the clinical use of circulating tumor DNA (ctDNA) in solid tumors, especially in different types of gastrointestinal cancer. As such, appraisal of the current and potential clinical utility of ctDNA is needed to guide clinicians in decision-making to facilitate its general applicability. In this review, we firstly discuss considerations surrounding specimen collection, processing, storage, and analysis, which affect reporting and interpretation of results. Secondly, we evaluate a selection of studies on colorectal, esophago-gastric, and pancreatic cancer to determine the level of evidence for the use of ctDNA in disease screening, detection of molecular residual disease (MRD) and disease recurrence during surveillance, assessment of therapy response, and guiding targeted therapy. Lastly, we highlight current limitations in the clinical utility of ctDNA and future directions. Current evidence of ctDNA in gastrointestinal cancer is promising but varies depending on its specific clinical role and cancer type. Larger prospective trials are needed to validate different aspects of ctDNA clinical utility, and standardization of collection protocols, analytical assays, and reporting guidelines should be considered to facilitate its wider applicability.en_US
dc.language.isoeng-
dc.titleA Practical Approach to Interpreting Circulating Tumor DNA in the Management of Gastrointestinal Cancers.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleClinical Chemistryen_US
dc.identifier.affiliationDivision of Cancer Research, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia.;Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationDivision of Personalised Oncology, the Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationSir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Victoria, Australia.;Division of Personalised Oncology, the Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.;Department of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia.en_US
dc.identifier.affiliationDivision of Surgery, Anaesthesia and Procedural Medicineen_US
dc.identifier.doi10.1093/clinchem/hvad188en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-9244-2057en_US
dc.identifier.orcid0000-0001-9283-9978en_US
dc.identifier.pubmedid38175583-
dc.description.volume70-
dc.description.issue1-
dc.description.startpage49-
dc.description.endpage59-
dc.subject.meshtermssecondaryCirculating Tumor DNA/genetics-
dc.subject.meshtermssecondaryGastrointestinal Neoplasms/diagnosis-
dc.subject.meshtermssecondaryGastrointestinal Neoplasms/genetics-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptSurgery-
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