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. 2021 Sep 10;13(18):4557. doi: 10.3390/cancers13184557

Table 1.

The clinical characteristics of the patients with CLL included in this study.

Patient No. Gender Age (Years) Time from Diagnosis (Years) Immunophenotype Mutations Treatment
del(13q) +12 del(11q) del(17p) IGHV
1 M 60 10 CLL Negative Negative Negative Negative ND None
2 M 68 1 CLL Negative Negative Negative Negative ND None
3 F 71 16 CLL ND ND ND ND ND None
4 M 65 11 CLL Negative Positive Negative Negative U None
5 M 58 10 CLL Positive Negative Positive Negative ND Yes
6 M 38 8 CLL Positive Negative Negative Negative U Yes
7 M 54 11 CLL Positive Negative Negative Negative U Yes
8 M 66 0 CLL Positive Negative Negative Positive U Yes
9 M 81 10 CLL Positive Negative Negative Negative ND Yes
10 M 87 1 CLL ND ND ND ND ND None
11 F 80 0 CLL Positive Negative Positive Negative U Yes
12 F 55 2 CLL Positive Negative Negative Negative Mut None
13 M 66 16 CLL Positive Negative Negative Negative ND None
14 M 66 10 CLL Positive Positive Negative Negative Mut Yes
15 F 63 11 CLL Positive Negative Negative Negative U Yes
16 M 79 7 CLL Positive Negative Negative Negative Mut Yes
17 M 73 0 CLL Negative Negative Negative Positive U Yes
18 F 64 5 CLL Positive Negative Negative Positive U Yes
19 M 44 4 CLL Positive Negative Negative Negative U Yes
20 F 72 6 CLL ND ND ND ND ND None
21 M 73 0 CLL Negative Positive Negative Negative U Yes
22 M 79 4 CLL Negative Negative Negative Negative ND Yes
23 M 52 8 CLL Positive Negative Negative Negative Mut None
24 M 63 1 aCLL/MCL Negative Negative Negative Negative ND Yes
25 F 64 4 CLL Positive Negative Positive Negative U None
26 M 75 10 CLL Positive Negative Negative Negative Mut Yes
27 M 71 1 CLL ND ND ND ND ND None
28 F 56 15 CLL Negative Negative Positive Negative U Yes

CLL, chronic lymphocytic leukemia; aCLL/MCL, atypical chronic lymphocytic leukemia/mantle cell lymphoma; IGHV, immunoglobulin heavy-chain variable region gene; M, male; F, female; ND, not determined; U, unmutated; Mut, mutated; del(13q), deletion of long arm of chromosome 13; +12, trisomy of chromosome 12; del(11q), deletion of long arm of chromosome 11; del(17p), deletion of short arm of chromosome 17.