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. 2017 Nov 28;9:122. doi: 10.1186/s13148-017-0422-7

Table 1.

Patients’ characteristics according to cytogenetic risk groups

Cytogenetic risk groups Low (n = 64) Intermediate (n = 19) High (n = 30) Statistics (p)
Age at diagnosis, mean (±SD) 64.4 (± 9.4) 67.8 (± 8.2) 64.9 (± 10.7) NS
Age at study entry, mean (±SD) 68.7 (± 9.3) 72.2 (± 8.4) 69.7 (± 9.8) NS
Binet stage, No. of patients (%) 0.05
 A 50/64 (78.1%) 11/19 (57.9%) 16/30 (51.7%)
 B 8/64 (12.5%) 5/19 (26.3%) 11/30 (37.9%)
 C 6/64 (9.4%) 3/19 (15.8%) 3/30 (10.3%)
Lymphocytosis (Giga/L), mean (±SD) 30.7 (± 29.3) 74.7 (± 71.1) 49.6 (± 40.60) 0.006
IGHV mutational status, No. of patients (%) NS
Unmutated (≥ 98% homology) 1/22 (4.5%) 2/12 (16.7%) 3/10 (30%)
Mutated (< 98% homology) 21/22 (95.5%) 10/12 (83.3%) 7/10 (70%)
CD38 > 30%, No. of patients (%) 12/58 (20.7%) 9/19 (47.4%) 6/25 (24%) NS
LDT from diagnosis, median (months)a 48 24 17 0.0004
PFS, median (months)a > 120 72 40 0.003
TFS, median (months)a > 120 77 72 0.001

Abbreviations: NS not significant, No. number, SD standard deviation, IGHV immunoglobulin heavy-chain variable region, LDT lymphocyte doubling time, PFS progression-free survival, TFS treatment-free survival

aKaplan–Meier survival analysis