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Serial circulating tumour DNA analysis during multimodality treatment of locally advanced rectal cancer: a prospective biomarker study

dc.contributor.authorTie, Jeanne
dc.contributor.authorCohen, Joshua
dc.contributor.authorWang, Yuxuan
dc.contributor.authorLi, Lu
dc.contributor.authorChristie, Michael
dc.contributor.authorSimons, Koen
dc.contributor.authorElsaleh, Hany
dc.contributor.authorKosmider, Suzanne
dc.contributor.authorWong, Rachel
dc.contributor.authorYip, Desmond
dc.contributor.authorLee, Margaret
dc.contributor.authorTran, Ben
dc.date.accessioned2023-02-17T00:16:42Z
dc.date.issued2018
dc.date.updated2023-12-10T07:17:19Z
dc.description.abstractObjective For patients with locally advanced rectal cancer (LARC), adjuvant chemotherapy selection following surgery remains a major clinical dilemma. Here, we investigated the ability of circulating tumour DNA (ctDNA) to improve risk stratification in patients with LARC. Design We enrolled patients with LARC (T3/T4 and/or N+) planned for neoadjuvant chemoradiotherapy. Plasma samples were collected pretreatment, postchemoradiotherapy and 4–10 weeks after surgery. Somatic mutations in individual patient’s tumour were identified via massively parallel sequencing of 15 genes commonly mutated in colorectal cancer. We then designed personalised assays to quantify ctDNA in plasma samples. Patients received adjuvant therapy at clinician discretion, blinded to the ctDNA results. Results We analysed 462 serial plasma samples from 159 patients. ctDNA was detectable in 77%, 8.3% and 12% of pretreatment, postchemoradiotherapy and postsurgery plasma samples. Significantly worse recurrence-free survival was seen if ctDNA was detectable after chemoradiotherapy (HR 6.6; P<0.001) or after surgery (HR 13.0; P<0.001). The estimated 3-year recurrence-free survival was 33% for the postoperative ctDNA-positive patients and 87% for the postoperative ctDNA-negative patients. Postoperative ctDNA detection was predictive of recurrence irrespective of adjuvant chemotherapy use (chemotherapy: HR 10.0; P<0.001; without chemotherapy: HR 22.0; P<0.001). Postoperative ctDNA status remained an independent predictor of recurrence-free survival after adjusting for known clinicopathological risk factors (HR 6.0; P<0.001). Conclusion Postoperative ctDNA analysis stratifies patients with LARC into subsets that are either at very high or at low risk of recurrence, independent of conventional clinicopathological risk factors. ctDNA analysis could potentially be used to guide patient selection for adjuvant chemotherapy.
dc.description.sponsorshipAustralian National Health and Medical Research Council (GNT1026230), the National Institute of Health (CA62924, GM07309, and P30-CA006973), Virginia and D K Ludwig Fund for Cancer Research, The John Templeton Foundation, The Conrad R Hilton Foundation, The Sol Goldman Sequencing Facility at Johns Hopkins.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn0017-5749en_AU
dc.identifier.urihttp://hdl.handle.net/1885/285283
dc.language.isoen_AUen_AU
dc.publisherBMJ Publishing Group
dc.relationhttp://purl.org/au-research/grants/nhmrc/1026230
dc.rights© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2019
dc.sourceGut
dc.titleSerial circulating tumour DNA analysis during multimodality treatment of locally advanced rectal cancer: a prospective biomarker study
dc.typeJournal article
local.bibliographicCitation.issue4en_AU
local.bibliographicCitation.lastpage671en_AU
local.bibliographicCitation.startpage663en_AU
local.contributor.affiliationTie, Jeanne, Walter and Eliza Hall Institute of Medical Researchen_AU
local.contributor.affiliationCohen, Joshua, Johns Hopkins University School of Medicineen_AU
local.contributor.affiliationWang, Yuxuan, Johns Hopkins University School of Medicineen_AU
local.contributor.affiliationLi, Lu, Johns Hopkins University School of Medicineen_AU
local.contributor.affiliationChristie, Michael, Melbourne Healthen_AU
local.contributor.affiliationSimons, Koen, The University of Melbourneen_AU
local.contributor.affiliationElsaleh, Hany, College of Health and Medicine, ANUen_AU
local.contributor.affiliationKosmider, Suzanne, Western Hospitalen_AU
local.contributor.affiliationWong, Rachel, Eastern Healthen_AU
local.contributor.affiliationYip, Desmond, College of Health and Medicine, ANUen_AU
local.contributor.affiliationLee, Margaret, The Royal Melbourne Hospitalen_AU
local.contributor.affiliationTran, Ben, Royal Melbourne Hospitalen_AU
local.contributor.authoruidElsaleh, Hany, a225770en_AU
local.contributor.authoruidYip, Desmond, u5086006en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor321100 - Oncology and carcinogenesisen_AU
local.identifier.ariespublicationu5369653xPUB260en_AU
local.identifier.citationvolume68en_AU
local.identifier.doi10.1136/gutjnl-2017-315852en_AU
local.identifier.scopusID2-s2.0-85047767738
local.identifier.thomsonIDWOS:000471830300012
local.publisher.urlhttps://gut.bmj.com/en_AU
local.type.statusPublished Versionen_AU

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