Table 1.

CLL patient samples analyzed in Figure 2B-E 

IGHVRai at samplingHierarchical cytogeneticsTherapy
M-CLLU-CLL0I-IIIII-IVHigh riskOthersTreatedUntreated
CXCL12          
 % of Control, median (N) 31 (16) 26 (11) 26 (10) 34 (8) 34 (9) 24 (6) 34 (21) 32 (13) 30 (14) 
 P* <.0001 .0029 .002 .0015 .0117 .0014 <.0001 .0002 .0002 
CCL19          
 % of Control, median (N) 34 (16) 29 (11) 30 (10) 40 (8) 29 (9) 26 (6) 33 (21) 28 (13) 40 (14) 
 P* .0042 .001 .0488 .004 .0117 .0023 .0006 .0012 .004 
BM stroma          
 % of Control, median (N) 32 (4) 54 (11) 53 (1) 67 (6) 26 (8) 53 (7) 46 (8) 37 (13) 65 (2) 
 P* .0365 .002 — .023 .0148 .0313 .0041 .0005 — 
ECM          
 % of Control, median (N) 41 (6) 45 (4) 95 (1) 50 (4) 35 (5) 21 (3) 46 (7) 36 (6) 83 (4) 
 P* .0313 .0452 — .0419 .0133 0.0663 .0117 .0313 0.2069 
IGHVRai at samplingHierarchical cytogeneticsTherapy
M-CLLU-CLL0I-IIIII-IVHigh riskOthersTreatedUntreated
CXCL12          
 % of Control, median (N) 31 (16) 26 (11) 26 (10) 34 (8) 34 (9) 24 (6) 34 (21) 32 (13) 30 (14) 
 P* <.0001 .0029 .002 .0015 .0117 .0014 <.0001 .0002 .0002 
CCL19          
 % of Control, median (N) 34 (16) 29 (11) 30 (10) 40 (8) 29 (9) 26 (6) 33 (21) 28 (13) 40 (14) 
 P* .0042 .001 .0488 .004 .0117 .0023 .0006 .0012 .004 
BM stroma          
 % of Control, median (N) 32 (4) 54 (11) 53 (1) 67 (6) 26 (8) 53 (7) 46 (8) 37 (13) 65 (2) 
 P* .0365 .002 — .023 .0148 .0313 .0041 .0005 — 
ECM          
 % of Control, median (N) 41 (6) 45 (4) 95 (1) 50 (4) 35 (5) 21 (3) 46 (7) 36 (6) 83 (4) 
 P* .0313 .0452 — .0419 .0133 0.0663 .0117 .0313 0.2069 

CLL patient samples analyzed in Figure 2B-E were divided into groups based on their clinical and molecular characteristics. Stratification was based on IGHV mutational status (mutated [M-CLL] and unmutated [U-CLL] IGHV); Rai stage at sampling (groups 0/I-II/III-IV; stage II and IV); hierarchical cytogenetics [high risk (del 11q and del 17p) vs others (del 13q, normal karyotype, tris 12)]; and prior therapy (treated vs untreated). For full data, see supplemental Figure 2E-H. Results are summarized for each group in the following format: median percentage of control, number of samples (N), and statistical significance (P). Raw data (migration index [MI] values, supplemental Figure 2A-D) were analyzed by Wilcoxon matched-pairs signed rank test or ratio paired Student t test according to the data distribution. Significant P values are shown in bold.

—, Not applicable.

*

Control vs CK1 inhibitor treated MI; Wilcoxon matched-pairs signed rank test or ratio paired Student t test according to the data distribution.

Inhibitory effects were significantly different between groups.

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