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. Author manuscript; available in PMC: 2021 Aug 17.
Published in final edited form as: Leukemia. 2017 May 30;31(12):2815–2823. doi: 10.1038/leu.2017.164

Table 1.

Clinical characteristics of patients with CMML

Diagnosis a N Age median (years) Gender M/F Karyotype normal/abnormal (N) Sub-classification

MD-CMML (N) MP-CMML (N)

CMML-1 96 74 67/29 55/41 54 42
CMML-2 27 70 22/5 13/14 18 9
sAML 27 69 15/12 15/12 14 13
Total CMML 150 104/46 83/67 86 64
M4/M5b 64 59 34/30 41/16
JMMLc 92 19d 61/31 77/15
Sum 156

Abbreviations: CMML, chronic myelomonocytic leukemia; sAML, secondary acute myeloid leukemia; JMML, juvenile myelomonocytic leukemia; M, male; F, female; MD, myelodysplastic; MP, myeloproliferative; TDS, targeted deep sequencing; WES, whole-exome sequencing.

a

WHO 2008 CMML: 31 cases were analyzed by WES, 93 cases were analyzed by TDS and 26 cases were analyzed by Sanger sequencing.

b

TCGA cohort: 64 M4/M5 were analyzed by WES.

c

JMML: 13 out of 92 cases were sequenced by WES and all cases were analyzed by TDS.2

d

Median age in months. For cytogenetic information see Supplementary Table 3.