Table 1.
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.