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. 2017 Mar 1;12(3):e0172978. doi: 10.1371/journal.pone.0172978

Table 1. Biological and clinical characteristics of hiMBL (n = 156) and Binet A CLL (n = 107) cohorts at diagnosis.

Variable hiMBL n (%) CLL n (%) P
Median follow-up, months (range) 73 (1–307) 95 (3–250) 0.069
Clinical variables at diagnosis
  Age [years, median (range)] 68 (30–89) 63 (29–86) 0.0002
    ≤60 25 (16) 47 (44) 6.9x10-7
  Sex
    Male 86 (55) 66 (62) 0.18
  WBC (mean ± SD; x109/L) 11.8±2.5 22.2±13.1 1.5x10-12
  Absolute lymphocyte count (mean ± SD; x109/L) 7.0±1.7 16.6±12.3 4.2x10-12
  CLL-type cells (mean ± SD; x109/L) 3.1±1.2 12.0±11.1 1.4x10-12
  β2-microglobulin >3.5 mg/L* 17 (11) 12 (14) 0.33
  Treated 16 (10) 44 (41) 6.7x10-9
Biological variables at diagnosis
  IGHV homology [mean (25th-75th percentiles)] 94.0 (91.6–96) 96 (93–100) 2.7x10-5
  IGHV unmutated (homology ≥98%)* 28 (19) 46 (44) 1.5x10-5
  FISH*
    Normal 53 (40) 41 (43) 0.39
    del(11)(q22.3) 2 (2) 5 (5) 0.12
    +12 19 (15) 9 (9) 0.18
    del(13)(q14) 61 (47) 43 (45) 0.51
    del(17)(p13) 0 (-) 4 (4) 0.031

* β2-microglobulin was available in 154 (99%) hiMBL and 87 (81%) Binet A CLL cases; IGHV status was available in 149 (96%) hiMBL and 105 (98%) Binet A CLL cases. FISH analyses were performed in 131 (84%) hiMBL and 95 (89%) Binet A CLL cases.