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. 2021 Nov 4;11(11):2041. doi: 10.3390/diagnostics11112041

Table 1.

Patient characteristics.

Number of Patients (%)
(Total Number of Patients n = 73)
Sex
Male 42 (58)
Female 31 (42)
Median age at diagnosis (years) 63 (range 36–80)
Binet stage initial diagnosis
A 48 (66)
B 15 (21)
C 6 (8)
not available 4 (5)
Rai stage initial diagnosis
0 20 (27)
I–II 32 (44)
III–IV 6 (8)
not available 15 (21)
Binet stage sample acquisition
A 32 (44)
B 22 (30)
C 17 (23)
not available 2 (3)
Rai stage sample acquisition
0 12 (16)
I–II 38 (53)
III–IV 21 (28)
not available 2 (3)
IGHV mutational status
mutated 10 (59)
unmutated 7 (41)
CD38 expression
<20% 43 (59)
20–29% 3 (4)
≥30% 15 (21)
not available 12 (16)
Cytogenetics risk
favorable * 5 (7)
intermediate * 4 (5)
poor * 10 (14)
not available 54 (74)
TP53 mutation
Positive 3 (4)
negative 20 (27)
not available 50 (68)
Lymphocyte count (1/µL) 43,984 (range 5366–320,330)
Hb (g/dL) 12.7 (range 7.9–16.8)
Plt (1000/µL) 183 (range 14–346)
β-2 microglobuline (mg/L) 3.7 (range 1.7–9.7)

Hb: haemoglobin; plt: thrombocytes; * classical cytogenetic analyses were performed, and patient grouped accordingly: favorable: 12q trisomy, del 13q; intermediate: normal karyotype; poor: del17p, del11q.