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Serial monitoring of circulating tumour DNA on clinical outcome in myelodysplastic syndromes and acute myeloid leukaemia

Dear Editor, Diagnostic bone marrow (BM) DNA and matched plasma-derived circulating tumour DNA (ctDNA) demonstrated excellent correlations in myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML),1–4 and dynamic ctDNA monitoring contributes to predict relapse in MDS and AML patients unde...

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Published in:Clinical and translational medicine 2023-07, Vol.13 (7), p.e1349-n/a
Main Authors: Zhou, Xinping, Lang, Wei, Mei, Chen, Ren, Yanling, Ma, Liya, Jiang, Lingxu, Ye, Li, Xu, Gaixiang, Luo, Yingwan, Liu, Lixia, Cao, Shanbo, Qin, Jiayue, Tong, Hongyan
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Language:English
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Summary:Dear Editor, Diagnostic bone marrow (BM) DNA and matched plasma-derived circulating tumour DNA (ctDNA) demonstrated excellent correlations in myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML),1–4 and dynamic ctDNA monitoring contributes to predict relapse in MDS and AML patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).5 However, few researches are reported on the application of ctDNA dynamic monitoring assessments during the whole disease course in MDS and AML.1 Here, we assessed the feasibility and utility of ctDNA as a novel and minimally invasive biomarker based on targeted next-generation sequencing (NGS) to monitor treatment outcome, track clonal evolution and predict survival. To investigate the prognostic differences between mean ctDNA VAF and mean ctDNA concentration change from post- to pre-treatment, we compared the discrimination ability of the prognostic model with the concordance index (C-index). SEE PDF] In summary, our study revealed that serial plasma-derived ctDNA assessments can reflect treatment response, survival, and clonal evolution in adult MDS and AML as a minimally invasive method, which warrant the prospective use of ctDNA as a biomarker in disease monitoring.
ISSN:2001-1326
2001-1326
DOI:10.1002/ctm2.1349