Table 4

Comparison of clinical and cytogenetic data in CD5 versus CD5+ SMZL cases

CharacteristicCD5, N (median or %)CD5+, N (median or %)P
Age, y, ≥ 65 y (68) (67) .898 
Sex, male/female 0.85 1.05 .712 
Hemoglobin, g/dL, ≤ 12 g/dL (11) (11) .959 
β2-Microglobulin, > 3 mg/L 31/50 (62%) 16/24 (66.6%) .696 
LDH, > 450 mg/L 15/62 (24%) 10/24 (41%) .109 
WBCs, ×109/L, ≥ 10 × 109/L 100 (12 300) 32 (13 165) .316 
Lymphocytes, ×109/L, ≥ 5 × 109/L 95 (5300) 33 (6900) .454 
Villous lymphocytes 27/37 (73%) 12/18 (66.6%) .629 
IGHV mutated 30/50 (60%) 9/14 (64%) .771 
Median survival time, y 9.4 10.6 .898 
Cytogenetic findings    
    +3/+3q* 29/119 (24%) 16/39 (41%) .004§ 
    del(7q) 47/119 (39.5%) 13/39 (33%) .491 
    +12 7/119 (6%) 3/39 (7.7%) .709 
    14q32 9/119 (7%) 3/39 (7%) 1.000 
    del TP53 11/55 (20%) 6/20 (30%) .367 
    +18 8/119 (7%) 7/39 (18%) .038§ 
    6q 7/119 (6%) 9/39 (23%) .004§ 
Abnormal karyotype 90/119 (75.6%) 32/38 (84.2%) .269 
Single anomaly 28/90 (31%) 4/32 (12.5%) .040§ 
More than or equal to 3 alterations 46/90 (51%) 18/32 (56.3%) .073 
CharacteristicCD5, N (median or %)CD5+, N (median or %)P
Age, y, ≥ 65 y (68) (67) .898 
Sex, male/female 0.85 1.05 .712 
Hemoglobin, g/dL, ≤ 12 g/dL (11) (11) .959 
β2-Microglobulin, > 3 mg/L 31/50 (62%) 16/24 (66.6%) .696 
LDH, > 450 mg/L 15/62 (24%) 10/24 (41%) .109 
WBCs, ×109/L, ≥ 10 × 109/L 100 (12 300) 32 (13 165) .316 
Lymphocytes, ×109/L, ≥ 5 × 109/L 95 (5300) 33 (6900) .454 
Villous lymphocytes 27/37 (73%) 12/18 (66.6%) .629 
IGHV mutated 30/50 (60%) 9/14 (64%) .771 
Median survival time, y 9.4 10.6 .898 
Cytogenetic findings    
    +3/+3q* 29/119 (24%) 16/39 (41%) .004§ 
    del(7q) 47/119 (39.5%) 13/39 (33%) .491 
    +12 7/119 (6%) 3/39 (7.7%) .709 
    14q32 9/119 (7%) 3/39 (7%) 1.000 
    del TP53 11/55 (20%) 6/20 (30%) .367 
    +18 8/119 (7%) 7/39 (18%) .038§ 
    6q 7/119 (6%) 9/39 (23%) .004§ 
Abnormal karyotype 90/119 (75.6%) 32/38 (84.2%) .269 
Single anomaly 28/90 (31%) 4/32 (12.5%) .040§ 
More than or equal to 3 alterations 46/90 (51%) 18/32 (56.3%) .073 

WBC indicates white blood cells.

*

Karyotype and FISH information was used for the statistical analysis of +3/+3q.

Never as a single aberration.

Twelve of 28 patients carried 7q deletion as a single anomaly.

§

Significant difference (P < .05).

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