ID | Sex | Age | Rai stage | Mutation status | ALC (×109/L) | %CD5+ cd19+ | Cytogenetics | TP53 mutation | Treatment |
1 | Male | 67 | II | Mutated | 149 | 93,2 | Del17p, trisomy 13, t(8;14) | ND | F, Chl |
2 | Male | 68 | I | Unmutated | NA | 90 | Del13q14 | ND | R-CHOP, F |
3 | Female | 55 | ND | Unmutated | 46,6 | 97,2 | ND | ND | F, other lines unknown |
4 | Male | 42 | ND | Unmutated | 287 | 99,7 | Del11q | ND | Chl |
5 | Male | 75 | I | Unmutated | 127 | 93 | Del13q14 | ND | No |
6 | Male | 65 | ND | ND | 162,8 | 97,8 | ND | ND | F, other lines unknown |
7 | Male | 76 | III | Unmutated | 120 | 91 | Del11q | ND | Chl, CVP, F |
8 | Male | 81 | NA | ND | 136 | 97 | Del13q14 | ND | Chl, F |
9 | Female | 63 | 0 | Polyclonal | 34,6 | 92,2 | Normal | ND | No |
10 | Male | 59 | NA | Mutated | 155 | 87,9 | Del17p, trisomy 12 | ND | Chl, R-CVP, FCR, R |
11 | Male | 70 | NA | Mutated | 322,6 | 100 | Del13q14 | ND | Chl, FC, |
12 | Male | 27 | NA | Unmutated | 160,5 | 93,8 | Del13q14, Del11q, loss 6q | TP53 WT | No |
13 | Male | 60 | 0 | Mutated | 56,5 | 95,2 | ND | ND | No |
14 | Male | 75 | II | ND | 73,4 | 96,6 | Del13q14 | TP53 WT | No |
15 | Male | 52 | I | Unmutated | 99,9 | 91,1 | Del17p, loss 5q, 5q, 6 p, 10q, 13q, 14q, 15q, 18 p, Gain 10q, 12q, | ND | FCR |
16 | Male | 70 | NA | Unmutated | 422 | 92,8 | Del17p | ND | Chl, CVP, FCR |
17 | Female | 75 | 0 | ND | 28,5 | 92,9 | ND | ND | No |
18 | Female | 71 | I | Mutated | 31,7 | 90,5 | ND | ND | No |
19 | Female | 75 | 0 | Mutated | 43,4 | 94,1 | ND | ND | No |
20 | Male | 77 | II | Mutated | 68,4 | 95,2 | Del13q14 | TP53 WT | No |
21 | Male | 62 | 0 | Mutated | 80,1 | 92,1 | Del13q14 | TP53 WT | No |
22 | Female | 60 | 0 | Unmutated | 65,3 | 91,2 | Trisomy 12 | TP53 WT | No |
23 | Male | 75 | NA | Mutated | 84,1 | 91,8 | ND | ND | No |
24 | Female | 73 | I | Mutated | 36,9 | 89,9 | ND | ND | No |
25 | Female | 63 | I | Mutated | 110,3 | 92,6 | Del13q14, Trisomy 12 | ND | No |
26 | Male | 63 | 0 | Unmutated | 250,91 | 97,6 | Del11q | ND | No |
27 | Female | 51 | II | Mutated | 122,75 | 92,4 | Del13q14 | TP53 WT | Chl, Of |
28 | Female | 79 | 0 | Mutated | 83,8 | 93,5 | ND | TP53 WT | No |
29 | Male | 67 | IV | Unmutated | 333,7 | 96,8 | Normal | TP53 WT | No |
30 | Female | 54 | I | Mutated | 91,8 | 90,99 | loss X | TP53 WT | No |
31 | Male | 82 | NA | Unmutated | 34,6 | 93,74 | ND | ND | No |
32 | Male | 69 | II | Unmutated | 41,8 | 94,04 | Del13q14, Del11q | TP53 WT | No |
33 | Male | 63 | 0 | ND | 44,6 | 91,3 | ND | ND | No |
34 | Female | 73 | 0 | Mutated | 20,9 | 92,08 | Del13q14 | TP53 WT | No |
35 | Female | 91 | I | ND | 68,5 | 92,92 | ND | ND | No |
36 | Female | 69 | 0 | Mutated | 58,51 | 92,26 | Del13q14 | ND | No |
37 | Male | 66 | I | Mutated | 73,41 | 91,98 | Normal | ND | No |
38 | Female | 80 | 0 | Unmutated | 37,29 | 90,23 | ND | ND | No |
39 | Female | 86 | I | Mutated | 43,14 | 95,36 | ND | ND | No |
40 | Male | 77 | 0 | Mutated | 52,29 | 92,97 | Del13q14, 14q32-rearrangement | ND | No |
41 | Male | 70 | 0 | ND | 74,11 | 97,29 | ND | ND | No |
42 | Female | 67 | 0 | ND | 95,69 | 94,07 | ND | ND | No |
43 | Male | 82 | ND | ND | 83,66 | 91,85 | ND | ND | No |
44 | Male | 66 | ND | ND | 49,6 | 95,08 | ND | ND | No |
45 | Female | 54 | ND | Mutated | 76,84 | 94,52 | ND | ND | No |
46 | Female | 71 | II | Unmutated | 125,55 | 96,36 | Del13q14 | TP53 mut | Chl +R, Venetoclax (resistant) |
47 | Male | 80 | I | ND | 65,7 | 94 | Del13q14 | TP53 mut | Chl, Ibr (resistant) |
48 | Male | 61 | ND | ND | 76,65 | 91,7 | Del17p | ND | R-CVP, FCR, Ibr (resistant) |
49 | Male | 66 | III | ND | 114,82 | 96,39 | Del13q14, Del17p | TP53 mut | FCR |
50 | Male | 70 | ND | Unmutated | 36,48 | 87,57 | Del17p, Del11q, gain of 3p14,3p14,1, 11q24,2q25 | TP53 mut | No |
Treatment indications were in accordance with IWCLL criteria. Patients with no treatments were in a steady state under a ‘watch and wait’ regimen. Deletion of 17 p was determined by CGH-array. TP53 mutations were determined by Sanger sequencing. Chemorefractory samples were defined according to IWCLL 2008 criteria and were marked as refractory when patients did not respond or relapsed ≤6 months after fludarabine treatment. Ibrutinib and venetoclax refractory samples were obtained from patients that had an IWCLL-defined progression under maintenance treatment with ibrutinib or venetoclax.
ALC, Absolute leukocyte count; Chl, chlorambucil; F, fludarabine; FCR, fludarabine, cyclophosphamide and rituximab; Ibr, ibrutinib; ND, not determined; Of, ofatumumab; R, rituximab; R-CHOP, rituximab cyclophosphamide, doxorubicin, vincristine and prednisone; R-CVP, rituximab cyclophosphamide, vincristin and prednisone; WT, wild type.