Clinical and biological features of study patients
Characteristic . | MDS N = 70 . |
---|---|
Age, median (range), y | 81 (54-94) |
Male, n (%) | 51 (72.9) |
Female, n (%) | 19 (27.1) |
Hemoglobin, median (range), g/dL | 11.75 (7.6-17.8) |
WBC count, median (range), ×109/L | 4.58 (1.44-12.28) |
Neutrophil count, median (range), ×109/L | 2.41 (0.31-7.68) |
Platelet count, median (range), ×109/L | 154 (28-584) |
Presence PB blasts, n (%) | 2 (2.86) |
LDH, median (range) | 292 (111-487) |
BM blasts %, median (range) | 2 (0-19) |
RSs %, median (range) | 0 (0-90) |
Altered karyotype, n (%) | 20 (28.6) |
Very good cytogenetic IPSS-R risk group, n (%) | 6 (8.6) |
Good cytogenetic IPSS-R risk group, n (%) | 7 (10) |
Intermediate cytogenetic IPSS-R risk group, n (%) | 4 (5.7) |
Poor cytogenetic IPSS-R risk group, n (%) | 2 (2.9) |
Very poor cytogenetic IPSS-R risk group, n (%) | 1 (1.4) |
IPSS-R risk group | |
Very low, n (%) | 28 (40) |
Low, n (%) | 31 (44.3) |
Intermediate, n (%) | 7 (10) |
High, n (%) | 2 (2.9) |
Very high, n (%) | 2 (2.9) |
MDS subtype (WHO 2017) | |
MDS-SLD, n (%) | 1 (1.4) |
MDS-MLD, n (%) | 35 (50) |
MDS-RS-SLD, n (%) | 5 (7.1) |
MDS-RS-MLD, n (%) | 17 (24.3) |
MDS-del(5q), n (%) | 2 (2.9) |
MDS-EB-1, n (%) | 6 (8.6) |
MDS-EB-2, n (%) | 2 (2.9) |
MDS-U, n (%) | 2 (2.9) |
Number of patients with mutations, n (%) | 66 (94.3) |
Mutations per patient, median (range) | 3 (0-10) |
Mutated genes per patient, median (range) | 2 (0-6) |
cfDNA concentration, median (range), ng/plasma mL | 58.4 (10.6-91.4) |
Characteristic . | MDS N = 70 . |
---|---|
Age, median (range), y | 81 (54-94) |
Male, n (%) | 51 (72.9) |
Female, n (%) | 19 (27.1) |
Hemoglobin, median (range), g/dL | 11.75 (7.6-17.8) |
WBC count, median (range), ×109/L | 4.58 (1.44-12.28) |
Neutrophil count, median (range), ×109/L | 2.41 (0.31-7.68) |
Platelet count, median (range), ×109/L | 154 (28-584) |
Presence PB blasts, n (%) | 2 (2.86) |
LDH, median (range) | 292 (111-487) |
BM blasts %, median (range) | 2 (0-19) |
RSs %, median (range) | 0 (0-90) |
Altered karyotype, n (%) | 20 (28.6) |
Very good cytogenetic IPSS-R risk group, n (%) | 6 (8.6) |
Good cytogenetic IPSS-R risk group, n (%) | 7 (10) |
Intermediate cytogenetic IPSS-R risk group, n (%) | 4 (5.7) |
Poor cytogenetic IPSS-R risk group, n (%) | 2 (2.9) |
Very poor cytogenetic IPSS-R risk group, n (%) | 1 (1.4) |
IPSS-R risk group | |
Very low, n (%) | 28 (40) |
Low, n (%) | 31 (44.3) |
Intermediate, n (%) | 7 (10) |
High, n (%) | 2 (2.9) |
Very high, n (%) | 2 (2.9) |
MDS subtype (WHO 2017) | |
MDS-SLD, n (%) | 1 (1.4) |
MDS-MLD, n (%) | 35 (50) |
MDS-RS-SLD, n (%) | 5 (7.1) |
MDS-RS-MLD, n (%) | 17 (24.3) |
MDS-del(5q), n (%) | 2 (2.9) |
MDS-EB-1, n (%) | 6 (8.6) |
MDS-EB-2, n (%) | 2 (2.9) |
MDS-U, n (%) | 2 (2.9) |
Number of patients with mutations, n (%) | 66 (94.3) |
Mutations per patient, median (range) | 3 (0-10) |
Mutated genes per patient, median (range) | 2 (0-6) |
cfDNA concentration, median (range), ng/plasma mL | 58.4 (10.6-91.4) |
EB, excess blasts; LDH, lactate dehydrogenase; MLD, multilineage dysplasia; SLD, single lineage dysplasia; U, unclassifiable; WBC, white blood cells; WHO, World Health Organization.