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. 2024 Oct 28;12(11):2476. doi: 10.3390/biomedicines12112476

Table 1.

Clinical and genetic features and subsequent events in 51 patients with CMML.

Variable CMML
(n = 51)
CMML-1
(n = 34)
CMML-2
(n = 17)
p-Value
Age in years; median (range) 71 (35–88) 73 (35–88) 66 (53–80) 0.0647
Male; n (%) 36 (71) 25 (74) 11 (65) 0.532
Other malignancies; n (%) a 20 (39) 14 (41) 6 (35) 0.7672
Leukemic transformations; n (% LT) 14 (28) 4 (12) 10 (59) 0.0008
Overall survival; median months 42 129 29 0.0077
Genetic Analysis CMML
(n = 36)
CMML-1
(n = 23)
CMML-2
(n = 13)
AML
(n = 14)
Epigenetic regulation analysis; n (%)
TET2 16 (44) 12 (52) 4 (31) 3 (21)
ASXL1 15 (42) 8 (35) 7 (54) 8 (57)
DNMT3A 5 (14) 2 (9) 3 (23) 2 (14)
BCOR 2 (6) 0 (0) 2 (15) 2 (14)
EZH2 1 (3) 1 (4) 0 (0) 0 (0)
Spliceosome mutational analysis; n (%)
SRSF2 10 (28) 6 (26) 4 (31) 4 (29)
ZRSR2 7 (19) 5 (22) 2 (15) 2 (14)
U2AF1 1 (3) 1 (4) 0 (0) 0 (0)
Cellular signaling analysis; n (%)
NRAS 5 (14) 2 (9) 3 (23) 4 (29)
KRAS 3 (8) 1 (4) 2 (15) 2 (14)
CBL 1 (3) 1 (4) 0 (0) 0 (0)
FLT3 2 (6) 0 (0) 2 (15) 1 (7)
PTPN11 2 (6) 1 (4) 1 (8) 2 (14)
Other; n (%)
RUNX1 12 (33) 7 (30) 5 (38) 6 (43)
SETBP1 2 (6) 0 (0) 2 (15) 2 (14)
NPM1 3 (8) 1 (4) 2 (15) 2 (14)

a Patients with other cancers: prostate cancer (3), breast cancer (3), non-Hodgkin lymphoma (2), multiple cancers (2), and treatment-related cancers (2). Note on treatment: no treatment (11 patients), hydroxyurea (11 patients), decitabine (12 patients), azacitidine (11 patients), venetoclax with demethylating agents (2 patients), and various other protocols (4 patients). Special cases include 2 patients with treatment-related CMML and 5 who underwent allogeneic transplantation.