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. 2017 Sep 28;3(9):e00405. doi: 10.1016/j.heliyon.2017.e00405

Table 2.

Association between ALL patients’ clinical and laboratorial characteristics and Stathmin 1 expressiona.

Parameters All patients (n = 40) Stathmin 1
p-valueb
Low expression (n = 20) High expression (n = 20)
Age; median (range), y 27 (18–79) 37 (18–79) 23 (18–78) 0.01
Female; n (%) 12 (27.9) 8 (40) 4 (20) 0.17
Immunophenotype 0.43
 B-ALL (%) 32 (80) 17 (85) 15 (75)
 T-ALL (%) 8 (20) 3 (15) 5 (25)
BCR-ABL1 (%) 8 (20) 5 (25) 3 (15) 0.43
Hemoglobin; median, (range); g/dL 8.7 (5.2–15.8) 8.1 (5.3–15.8) 8.9 (5.2–12.8) 0.79
WBC; median (range) × 109/L 13.7 (0.8–549.5) 8.2 (1.1–92.1) 20.65 (0.8–549.5) 0.06
Platelets; median (range) × 109/L 36.5 (4–433) 38 (7–433) 32.5 (4–162) 0.56
LDH (range) U/L 1789 (245–13090) 1750 (245–6848) 1789 (270–13090) 0.32

Abbreviations: ALL, acute lymphoblastic leukemia; T-ALL, precursor T-acute lymphoblastic leukemia; B-ALL, precursor B-acute lymphoblastic leukemia; BCR-ABL1, breakpoint cluster region-abelson 1; WBC, white blood cell; LDH, lactic dehydrogenase.

Statistically significant p values are highlighted in bold.

a

Patients with ALL whose sample were collected at diagnosis (n = 40) were included in association analysis.

b

Mann–Whitney test and Fisher’s exact test were used for measured and categorical factors, respectively.