Table 1A: Clinical and haematological features | |
Characteristic | N (%) |
No. of patients with MDS | 988 |
Median age (range) | 53 years (18–86) |
No. of patients ≥ 21 years (%) | 899 (96) |
Median age of patients ≥ 21 years (range) | 53 years (21–86) |
No. of patients ≥ 40 years (%) | 696 (74) |
Median age of patients ≥ 40 years (range) | 58 years (40–86) |
Males / females (M: F ratio) | 607/329 (1.8:1) |
Blood counts | |
Hemoglobin, g/dL, n = 929 | |
<10 | 787(84.7) |
≥10 | 142(15.3) |
Platelet count, ×10⁹/L, n = 929 | |
<100,000 | 619(66.6) |
≥100,000 | 310(33.4) |
Absolute neutrophil count (ANC), ×10⁹/L, n = 919 | |
<0.8 | 610(66.4) |
≥0.8 | 309(33.6) |
Single cytopenia | 237(25.5) |
Anemia | 165(17.8) |
Thrombocytopenia | 51(5.5) |
Leucopenia | 21(2.3) |
Bicytopenia | 311(33.5) |
Anemia & thrombocytopenia | 165(18) |
Anemia & leucopenia | 98(10.7) |
Thrombocytopenia & leucopenia | 48(14.1) |
Pancytopenia | 346(37.6) |
Table 1B. Overview of cytogenetic findings | |
Characteristic | N (%) |
Successful cytogenetic analyses | 936 (94.7) |
Normal karyotypes | 421(44.9) |
Clonal cytogenetic abnormalities | 515(55) |
Numerical abnormalities only | 131 (25.4) |
Structural abnormalities only | 201(39) |
Numerical and structural abnormalities | 183 (35.5) |
Cytogenetic abnormalities | |
Single abnormality | 279(29.8) |
Two abnormalities | 70(7.5) |
≥2 independent non-complex clones | 25(2.7) |
Complex KT, ≥3 abnormalities | 141(15) |
Complex KT with 3 abnormalities | 36(3.8) |
Complex KT with >3 abnormalities | 105(11.2) |
Table 1C. Cytogenetic prognosis and clinical risk groups | |
Cytogenetic prognosis groups (as per CCSS and IPSS-R) | N (%) |
Very good prognosis | 19(2) |
Good prognosis, all / abnormal KT only | 520(55.6)/99(10.6) |
Intermediate prognosis | 152(16.2) |
Poor prognosis | 140(15) |
Very poor prognosis | 105(11.2) |
Clinical (IPSS-R) risk groups, n = 842 | N (%) |
Very low risk | 33(3.9) |
Low risk | 260(30.9) |
Intermediate risk | 204(24.2) |
High risk | 177(21) |
Very high risk | 168(20) |