Table 2. Clinical and laboratory characteristics of the B-CLL patients.
Pt.# | Therapy | %CD38+ cells† | %ZAP-70+ | Cytogenetic abnormalities* | IgVH status | TP53 status | IC50 Ibrutinib (μM) |
---|---|---|---|---|---|---|---|
1 | Untreated | neg | neg | del13q | mut | wild-type | 14.6 |
2 | Ibrutinib | neg | neg | del11q, del13q | unmut | muta | 11 |
3 | Untreated | neg | neg | trisomy 12 | mut | wild-type | 0.1 |
4 | Untreated | neg | neg | neg | mut | wild-type | 14.4 |
5 | Untreated | neg | neg | neg | mut | wild-type | 12.3 |
6 | Ibrutinib | pos | na | del11q, del13q | unmut | mutb | 17.7 |
7 | Untreated | pos | pos | del13q | unmut | wild-type | 10.2 |
8 | Untreated | neg | neg | del13q | mut | wild-type | 12.5 |
9 | R-Benda | pos | neg | del13q | unmut | wild-type | 11.2 |
10 | Untreated | neg | neg | na | mut | wild-type | 5.3 |
11 | Untreated | pos | neg | del13q | mut | wild-type | 11.8 |
12 | Ibrutinib | neg | neg | del11q, del17p, del13q | unmut | mutc | 4.4 |
13 | Chl | pos | neg | neg | unmut | wild-type | 3.1 |
14 | Untreated | neg | na | neg | na | wild-type | 35.9 |
15 | Untreated | neg | neg | del13q | mut | wild-type | 5.2 |
16 | R-Benda | neg | neg | del13q | mut | wild-type | 2.5 |
17 | FC, FCR, R-Benda | neg | neg | del11q, del13q | na | wild-type | 8.1 |
18 | Untreated | pos | na | trisomy 12 | mut | wild-type | 10.5 |
19 | Untreated | pos | na | trisomy 12 | na | na | 7.1 |
20 | Untreated | neg | neg | neg | mut | wild-type | 2.9 |
21 | Untreated | neg | na | del13q | na | na | 15 |
22 | Ibrutinib | neg | na | del13q | unmut | wild-type | 17.6 |
Pt., patient; R-Benda, Rituximab-Bendamustine; Chl, Chlorambucil; FC, Fludarabine-Chlorambucil; FCR, Fludarabine-Chlorambucil-Rituximab; neg, negative; pos, positive; na, not available; mut, mutated; unmut, unmutated.
Results obtained in cytometric assays, using a CD38 cutoff of 30%.
Cytogenetic abnormalities were evaluated by fluorescence in situ hybridization (FISH) analysis.
c.394A>G:p.K132E;
c.644G>A:p.S215N;
c.770T>C:p.L257P.