Comparison of myeloid blast counts and variant allele frequencies of gene mutations in myelodysplastic syndrome with excess blasts and secondary acute myeloid leukemia

被引:26
作者
Chen, Xueyan [1 ]
Othus, Megan [2 ]
Wood, Brent L. [1 ]
Walter, Roland B. [2 ,3 ]
Becker, Pamela S. [2 ,3 ]
Percival, Mary-Elizabeth [2 ,3 ]
Abkowitz, Janis L. [3 ]
Appelbaum, Frederick R. [2 ]
Estey, Elihu H. [2 ,3 ]
机构
[1] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, Mail Stop LG-540,1100 Fairview Ave N, Seattle, WA 98109 USA
[3] Univ Washington, Dept Med, Div Hematol, Seattle, WA 98195 USA
关键词
Acute myeloid leukemia; myelodysplastic syndromes; genetic mutations; variant allele frequency;
D O I
10.1080/10428194.2020.1861267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Secondary acute myeloid leukemia (sAML) is biologically and clinically distinct from de novo AML and shares specific genetic mutations with myelodysplastic syndromes (MDS). We retrospectively analyzed data from 295 adults with MDS or AML with mutational analysis by next-generation sequencing (NGS), and examined differences in functional grouping of mutations and relation between morphologic blast count and variant allele frequency (VAF) of mutations. Our analysis showed the distribution of mutations differed in MDS and AML. However, these differences largely disappeared when we compared MDS with excess blasts (MDS-EB) and sAML. VAF of mutations generally did not correlate with morphologic blast count and the distribution of VAF was similar above and below the 20% cutpoint. Complete remission (CR) rate was similar in MDS-EB and sAML following high intensity therapy and survival was also similar. These results support that MDS-EB and sAML have overlapping features and may represent a spectrum of the same disease.
引用
收藏
页码:1226 / 1233
页数:8
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