Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/122834
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dc.contributor.authorPagani, I.S.en
dc.contributor.authorDang, P.en
dc.contributor.authorSaunders, V.A.en
dc.contributor.authorGrose, R.en
dc.contributor.authorShanmuganathan, N.en
dc.contributor.authorKok, C.H.en
dc.contributor.authorCarne, L.en
dc.contributor.authorRwodzi, Z.en
dc.contributor.authorWatts, S.en
dc.contributor.authorMcLean, J.en
dc.contributor.authorBraley, J.en
dc.contributor.authorAltamura, H.en
dc.contributor.authorYeung, D.T.en
dc.contributor.authorBranford, S.en
dc.contributor.authorYong, A.S.M.en
dc.contributor.authorWhite, D.L.en
dc.contributor.authorHughes, T.P.en
dc.contributor.authorRoss, D.M.en
dc.date.issued2020en
dc.identifier.citationLeukemia, 2020; 34(4):1052-1061en
dc.identifier.issn0887-6924en
dc.identifier.issn1476-5551en
dc.identifier.urihttp://hdl.handle.net/2440/122834-
dc.descriptionPublished: 25 November 2019en
dc.description.abstractApproximately half of patients with chronic myeloid leukemia (CML) in sustained deep molecular response who discontinue tyrosine kinase inhibitors (TKIs) remain in treatment-free remission (TFR). Some of these patients have measurable residual disease (MRD) by BCR-ABL1 mRNA testing, and most have detectable BCR-ABL1 DNA by highly sensitive methods. We used fluorescence-activated cell sorting and BCR-ABL1 DNA PCR to investigate the lineage of residual CML cells in TFR. Twenty patients in TFR for >1 year provided blood for sorting into granulocytes, monocytes, B cells, T cells, and NK cells. MRD was identified predominantly in the lymphoid compartment and never in granulocytes. B cells were more often BCR-ABL1 positive than T cells (18 vs 11/20 patients) and at higher levels (median 10-4.9 vs 10-5.7; P = 0.014). In 13 CML patients studied at diagnosis lymphocytes expressing BCR-ABL1 mRNA comprised a small proportion of total leukocytes. These data improve our understanding of TFR biology, since it is now clear that MRD in the blood of TFR patients need not imply the persistence of multipotent CML cells. Lineage-specific assessment of MRD could be explored as a means to improve the prediction of TFR.en
dc.description.statementofresponsibilityIlaria S. Pagani, Phuong Dang, Verity A. Saunders, Randall Grose, Naranie Shanmuganathan, Chung H. Kok … et al.en
dc.language.isoenen
dc.publisherSpringer Natureen
dc.rights© The Author(s), under exclusive licence to Springer Nature Limited 2019.en
dc.subjectLymphocyte Subsets; Humans; Neoplasm, Residual; Fusion Proteins, bcr-abl; Protein Kinase Inhibitors; Prognosis; Remission Induction; Follow-Up Studies; Cell Lineage; Adult; Aged; Aged, 80 and over; Middle Aged; Female; Male; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Imatinib Mesylateen
dc.titleLineage of measurable residual disease in patients with chronic myeloid leukemia in treatment-free remissionen
dc.typeJournal articleen
dc.identifier.rmid1000006485en
dc.identifier.doi10.1038/s41375-019-0647-xen
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1138935en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1104425en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1051965en
dc.identifier.pubid507577-
pubs.library.collectionMedicine publicationsen
pubs.library.teamDS10en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidPagani, I.S. [0000-0002-3216-2966]en
dc.identifier.orcidShanmuganathan, N. [0000-0001-5895-8797]en
dc.identifier.orcidKok, C.H. [0000-0002-3181-7852]en
dc.identifier.orcidYeung, D.T. [0000-0002-7558-9927]en
dc.identifier.orcidBranford, S. [0000-0002-1964-3626]en
dc.identifier.orcidYong, A.S.M. [0000-0001-9452-1533]en
dc.identifier.orcidWhite, D.L. [0000-0003-4844-333X]en
dc.identifier.orcidHughes, T.P. [0000-0002-0910-3730]en
dc.identifier.orcidRoss, D.M. [0000-0001-7171-2935]en
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