Journal article
Circulating tumour DNA reflects treatment response and clonal evolution in chronic lymphocytic leukaemia
P Yeh, T Hunter, D Sinha, S Ftouni, E Wallach, D Jiang, YC Chan, SQ Wong, MJ Silva, R Vedururu, K Doig, E Lam, GM Arnau, T Semple, M Wall, A Zivanovic, R Agarwal, P Petrone, K Jones, D Westerman Show all
Nature Communications | Published : 2017
DOI: 10.1038/ncomms14756
Abstract
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..
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Grants
Awarded by National Health and Medical Research Council
Funding Acknowledgements
P.Y. is supported by the Klempfner Epigenetics Fellowship administered by the Snowdome Foundation and by the Haematology Society of Australia and New Zealand new investigator scholarship. A National Breast Cancer Foundation and Victorian Cancer Agency Fellowship currently support S.J.D. The National Health and Medical Research Council of Australia (1104549) supported this research. The clinical study patient recruitment was funded by Abbvie and Janssen. We thank Sreeja Gadipally and Timothy Holloway for assistance with exome sequencing and LC-WGS.