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dc.contributor.authorvan der Linde, R.-
dc.contributor.authorGatt, P. N.-
dc.contributor.authorSmith, S.-
dc.contributor.authorFernandez, M.-
dc.contributor.authorVaughan, Lachlin-
dc.contributor.authorBlyth, Emily M.-
dc.contributor.authorCurnow, Jennifer-
dc.contributor.authorBrown, David A.-
dc.contributor.authorTegg, Elizabeth-
dc.contributor.authorSasson, Sarah C.-
dc.date.accessioned2024-04-23T04:29:47Z-
dc.date.available2024-04-23T04:29:47Z-
dc.date.issued2024-
dc.identifier.citationPathology 56(Supplement 1):S108, 2024-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9471-
dc.description.abstractMeasurable residual disease (MRD) detected by flow cytometry (FC) is well established in paediatric B- lymphoblastic leukaemia (B-ALL) and adult chronic lymphocytic leukaemia (CLL), but its utility in adult B-ALL and adult acute myeloid leukaemia (AML) is less clear. In this prospective MRD study we examined consecutive bone marrow aspirates from adult participants with B-ALL (n=47) and AML (n=87) sent for FC-MRD testing at a quaternary referral hospital in Sydney. FC-MRD RESULTS were correlated to corresponding molecular MRD (Mol-MRD) testing where available and clinical outcomes at three-month intervals over 1 year. B-ALL showed a moderate positive correlation (rs=0.401, p<0.001), while there was no correlation between FC-MRD and Mol-MRD for AML (rs=0.13, p=0.237). Five longitudinal FC-MRD patterns were identified which had significant associations with relapse (chi2(4)=31.17(4), p>0.001) and survival (chi 2(4)=13.67, p=0.008) in AML, but not in B-ALL. MRD level at 3 months was strongly associated with relapse and survival in AML, while the association in B-ALL was less evident. Overall, these findings suggest divergent utilities of FC-MRD in AML and B-ALL.-
dc.subjectHaematology-
dc.subjectOncology-
dc.titleCorrelation of flow cytometric measurable residual disease (FC-MRD) with molecular MRD and clinical outcome at one year in adult B-acute lymphoblastic leukaemia (B-ALL) and acute myeloid leukaemia (AML)-
dc.typeJournal Article-
dc.identifier.doihttps://dx.doi.org/10.1016/j.pathol.2023.12.359-
dc.subject.keywordsleukemia, acute myeloid-
dc.subject.keywordsB cell acute lymphoblastic leukemia-
dc.subject.keywordsbone marrow aspiration-
dc.subject.keywordschronic lymphatic leukemia-
dc.subject.keywordsacute disease-
dc.identifier.journaltitlePathology-
dc.identifier.departmentPathology-
dc.identifier.departmentHaematology-
dc.identifier.departmentImmunology-
dc.contributor.wslhdVaughan, Lachlin-
dc.contributor.wslhdBlyth, Emily M.-
dc.contributor.wslhdCurnow, Jennifer-
dc.contributor.wslhdBrown, David A.-
dc.contributor.wslhdTegg, Elizabeth-
dc.contributor.wslhdSasson, Sarah C.-
dc.type.studyortrialProspective Study-
dc.identifier.affiliationNSW Health Pathology, NSW, Australia-
dc.identifier.affiliationDepartment of Clinical Haematology, Western Sydney Local Health District, NSW, Australia-
dc.identifier.facilityBlacktown-
dc.identifier.facilityWestmead-
dc.identifier.conferencenamePATHOLOGY UPDATE 2024 ABSTRACTS SUPPLEMENT. Adelaide Australia.-
Appears in Collections:Blacktown Mount Druitt Hospital

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