Table 1 Clinicobiological characteristics of the studied cohort.

From: Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY

 

All cases

Binet A

Binet A M-CLL

Binet A U-CLL

Gender

  Male

2890 (63%)

1992 (59%)

1183 (58%)

708 (61%)

  Female

1690 (37%)

1370 (41%)

862 (42%)

445 (39%)

Median age at diagnosis (years)

64.6

64.9

64.6

64.9

IGHV gene SHM status

  M-CLL

2454 (57%)

2045 (64%)

  

  U-CLL

1878 (43%)

1153 (36%)

  

  Unknown

239

164

  

Recurrent aberrationsa

  del(13q)

1856 (42%)

1465 (45%)

775 (57%)

302 (27%)

  trisomy12

566 (13%)

380 (12%)

72 (5%)

212 (19%)

  del(11q)

495 (11%)

277 (8%)

12 (1%)

225 (20%)

  del(17p)

236 (5%)

148 (5%)

42 (3%)

78 (7%)

  No recurrent abnormalities

1306 (29%)

1005 (31%)

469 (34%)

319 (28%)

  Unknown

121

87

35

17

Binet stage

  A

3362 (74%)

   

  B

825 (18%)

   

  C

387 (8%)

   

  Unknown

6

   

Treatment statusb

  Treated

2680 (59%)

1570 (47%)

640 (32%)

875 (76%)

  Untreated

1900 (41%)

1792 (53%)

1405 (68%)

278 (24%)

  1. SHM somatic hypermutation, M-CLL CLL with mutated IGHV genes, U-CLL CLL with unmutated IGHV genes.
  2. aAccording to the Döhner classification [6].
  3. bAt follow-up.