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. Author manuscript; available in PMC: 2016 Jul 1.
Published in final edited form as: J Geriatr Oncol. 2015 Jun 11;6(4):288–298. doi: 10.1016/j.jgo.2015.05.003

Table 1.

Demographic and clinico-pathological characteristics of patients with MDS (n = 114).

Characteristic N (%)a
Age category
 65–69   34 (29.8)
 70–74   35 (30.7)
 75–79   22 (19.3)
 80+   23 (20.2)
Male   85 (74.6)
White 108 (94.7)
Lives alone   13 (11.8)
History of tobacco use   65 (57.0)
WHO BMI categories
 <25   30 (27.1)
 25–30   48 (43.2)
 >30   33 (29.7)
Baseline ECOG Performance Status
 0   51 (44.7)
 1   49 (43.0)
 ≥2   14 (12.3)
Baseline Charlson comorbidity score
 0   43 (37.7)
 1   19 (16.7)
 2   30 (26.3)
 ≥3   22 (19.3)
Serum albumin <3.5 g/dl   11 (9.7)
Number of cytopeniasd
 0   16 (14.0)
 1   36 (31.6)
 2   39 (34.2)
 3   23 (20.2)
Cytogeneticse
 Good   76 (66.6)
 Intermediate   19 (16.7)
 Poor   19 (16.7)
% Bone marrow blastsf
 <5%   74 (66.1)
 5–10%   27 (24.1)
 >10%   11 (9.8)
IPSS Category
 Low risk   27 (23.7)
 Intermediate risk-1   52 (45.6)
 Intermediate risk-2   30 (26.3)
 High risk     5 (4.4)
Previous chemotherapy or radiation   20 (17.5)
Treatment type received
 No chemotherapy   53 (46.5)
 Non-intensive chemotherapyb   44 (38.6)
 Intensive chemotherapyc   17 (14.9)
a

May not add up to 100% due to missing variables.

b

5-Azacytidine or decitabine.

c

Induction chemotherapy and/or non-myeloablative bone marrow transplant.

d

Component of the IPSS score. Platelets < 100,000/μl; hemoglobin < 10 g/dl; neutrophils < 1800/μl.

e

Component of the IPSS score. Good: normal, -Y, del(5q), del(20q); intermediate: other abnormalities; poor: complex (≥3 abnormalities) or chromosome 7 anomalies.

f

Component of the IPSS score.