Circulating tumour DNA reflects treatment response and clonal evolution in chronic lymphocytic leukaemia

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作者
Paul Yeh
Tane Hunter
Devbarna Sinha
Sarah Ftouni
Elise Wallach
Damian Jiang
Yih-Chih Chan
Stephen Q. Wong
Maria Joao Silva
Ravikiran Vedururu
Kenneth Doig
Enid Lam
Gisela Mir Arnau
Timothy Semple
Meaghan Wall
Andjelija Zivanovic
Rishu Agarwal
Pasquale Petrone
Kate Jones
David Westerman
Piers Blombery
John F. Seymour
Anthony T. Papenfuss
Mark A. Dawson
Constantine S. Tam
Sarah-Jane Dawson
机构
[1] Peter MacCallum Cancer Centre,Division of Cancer Research
[2] Peter MacCallum Cancer Centre,Division of Cancer Medicine
[3] University of Melbourne,Sir Peter MacCallum Department of Oncology
[4] Peter MacCallum Cancer Centre,Department of Radiology
[5] Victorian Cancer Cytogenetics Service,Department of Medicine
[6] St Vincent’s Hospital,Department of Haematology
[7] St Vincent’s Hospital,undefined
[8] University of Melbourne,undefined
[9] Walter and Eliza Hall Institute of Medical Research,undefined
[10] Centre for Cancer Research,undefined
[11] University of Melbourne,undefined
[12] St Vincent’s Hospital,undefined
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摘要
Several novel therapeutics are poised to change the natural history of chronic lymphocytic leukaemia (CLL) and the increasing use of these therapies has highlighted limitations of traditional disease monitoring methods. Here we demonstrate that circulating tumour DNA (ctDNA) is readily detectable in patients with CLL. Importantly, ctDNA does not simply mirror the genomic information contained within circulating malignant lymphocytes but instead parallels changes across different disease compartments following treatment with novel therapies. Serial ctDNA analysis allows clonal dynamics to be monitored over time and identifies the emergence of genomic changes associated with Richter’s syndrome (RS). In addition to conventional disease monitoring, ctDNA provides a unique opportunity for non-invasive serial analysis of CLL for molecular disease monitoring.
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