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. 2016 Aug 4;7(39):63177–63188. doi: 10.18632/oncotarget.11050

Table 1. Comparison of clinical and laboratory features between h-MDS and NH-MDS patients.

Clinical characters Total (n=369) h-MDS (n=100, 27.1%) NH-MDS (n=269, 72.9%) P value
Sex 0.324
Male 242 (65.6%) 70 (70.0%) 172 (63.9%)
Female 127 (34.4%) 30 (30.0%) 97 (36.1%)
Age (year)* 65.2 (16.4-94.5) 61.6 (18.4-94.5) 65.3 (16.4-90.5) 0.997
Lab data**
WBC (/μL) 3490 (490-40500) 3050 (650-9890) 3660 (490-40500) 0.030*
Hb (g/dL) 8.1 (3.4-14.6) 8.1 (3.7-14.4) 8.2 (3.2-14.6) 0.971
Platelet (×1,000 /μL) 77 (3-931) 66 (3-618) 82 (3-931) 0.179
LDH (U/L) 482 (145-6807) 463 (145-3122) 495 (210-6807) 0.361
PB blast count (/μL) 0 (0-3270) 0 (0-523) 0 (0-3270) 0.006*
BM blast % 3.2 (0-19.0) 2.0 (0-19.0) 4.5 (0-19.5) 0.001*
2008 WHO classification#
RCUD 75 (20.3%) 28 (28.0%) 47 (17.5%) 0.029*
RARS 20 (5.4%) 3 (3.0%) 17 (6.3%) 0.302
RCMD 94 (25.5%) 38 (38.0%) 56 (20.8%) 0.001*
RCMD-RS 14 (3.8%) 3 (3.0%) 11 (4.1%) 0.767
RAEB1 78 (21.1%) 11 (11.0%) 67 (24.9%) 0.004*
RAEB2 85 (23.1%) 17 (17.0%) 68 (25.3%) 0.097
MDS-U 3 (0.8%) 0 (0%) 3 (1.1%) 0.566
IPSS#§ <0.001*
Low+INT-1 219 (64.2%) 72 (80.0%) 147 (58.6%)
INT-2+High 122 (35.8%) 18 (20.0%) 104 (41.4%)
IPSS-R#ζ 0.001*
Very low+low+INT 197 (57.8%) 65 (72.2%) 132 (52.6%)
High+very high 144 (42.2%) 25 (27.8%) 119 (47.4%)
Treatment modalities
Transfusion/BCS 235 (63.7%) 70 (70.0%) 165 (61.3%) 0.144
HMA 20 (5.4%) 4 (4.0%) 16 (5.9%) 0.608
Intensive chemotherapy 26 (7.1%) 2 (2.0%) 24 (8.9%) 0.021*
Lose-dose chemotherapy 37 (10.0%) 7 (7.0%) 30 (11.2%) 0.329
HSCT 51 (13.8%) 17 (17.0%) 34 (12.6%) 0.309
**

Median (range).

*

Statistically significant if P<0.05.

#

Number of patients (% of patients within either hypoplastic or non-hypoplastic MDS subgroups).

341patients, including 90 h-MDS and 251 NH-MDS patients, had chromosome data at diagnosis.

§

IPSS: Low, 0; intermediate (INT)-1, 0.5-1; INT-2, 1.5-2; and High, ≥ 2.5.

ζ

IPSS-R: Very low, ≦1.5; Low, >1.5-3; intermediate (INT),>3-4.5; High, >4.5-6; and Vey high, >6.

Abbreviations: h-MDS, hypoplastic MDS; NH-MDS, normo-/hypercellular MDS; FAB, French-American-British classification; RARS, refractory anemia with ring sideroblasts; RAEB, refractory anemia with excess blasts; RCUD, refractory cytopenia with unilineage dysplasia; RCMD, refractory cytopenia with multilineage dysplasia; and MDS-U, MDS (unclassifiable); IPSS, international prognosis scoring system; IPSS-R, revised IPSS.