期刊
BLOOD
卷 129, 期 1, 页码 38-47出版社
AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2016-04-708560
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资金
- Basic Science Research Program through the National Research Foundation of Korea (NRF)
- Ministry of Science, ICT and Future Planning [NRF-2015R1A2A1A10054579, NRF-2011-0030034]
- Foreign Research Institute Recruitment Program through the NRF
- Queen Elizabeth II Graduate Scholarship for Science and Technology (University of Toronto)
Somatic mutations commonly detected in a variety of myeloid neoplasms have not been systematically investigated in chronic myeloid leukemia (CML). We performed targeted deep sequencing on a total of 300 serial samples from 100 CML patients; 37 patients carried mutations. Sixteen of these had evidence of mutations originating from preleukemic clones. Using unsupervised hierarchical clustering, we identified 5 distinct patterns of mutation dynamics arising following tyrosine kinase inhibitor (TKI) therapy. This study demonstrates that patterns of mutation acquisition, persistence, and clearance vary but have a number of interesting correlations with clinical outcomes. Mutation burden often persisted despite successful TKI response (pattern 1), providing indirect evidence that these mutations also originated from preleukemic mutations, whereas patients exhibiting mutation clearance (pattern 3) showed mixed clinical outcomes. Unsurprisingly, patients acquiring new mutations during treatment failed TKI therapy (pattern 2). These patterns show that CML mutation dynamics following TKI therapy are markedly distinct from other myeloid neoplasms. In summary, clinical implications of mutation profiles and dynamics in CML should be interpreted with caution.
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