Figure 3
Figure 3. PTK7 expression is associated with poor clinical outcome. (A) Correlation between PTK7 expression and WBC at diagnosis. The PTK7+ AMLs are significantly associated with lower WBC count in the whole population (Wilcoxon test, P = .001) but also when myeloid and monocytic subgroups were analyzed separately. (B) Correlation of PTK7 expression and extramedullary disease. LN indicates lymph node involvement; S&L, spleen and/or liver enlargement; and EHD, extrahematologic disease. Frequency was lower in PTK7+ AML (χ2 test, P < .001, .01, < .001, and < .001 for the respective columns), and this was also confirmed in analysis of subgroup patients. (C-E) Survival curves (OS and LFS, time scale is in months) using the Kaplan-Meier method. Only patients with homogeneous treatment were analyzed (n = 182). Differences shown here were confirmed in the Cox multivariate analysis model. (E) OS in intermediate cytogenetic risk group patients.

PTK7 expression is associated with poor clinical outcome. (A) Correlation between PTK7 expression and WBC at diagnosis. The PTK7+ AMLs are significantly associated with lower WBC count in the whole population (Wilcoxon test, P = .001) but also when myeloid and monocytic subgroups were analyzed separately. (B) Correlation of PTK7 expression and extramedullary disease. LN indicates lymph node involvement; S&L, spleen and/or liver enlargement; and EHD, extrahematologic disease. Frequency was lower in PTK7+ AML (χ2 test, P < .001, .01, < .001, and < .001 for the respective columns), and this was also confirmed in analysis of subgroup patients. (C-E) Survival curves (OS and LFS, time scale is in months) using the Kaplan-Meier method. Only patients with homogeneous treatment were analyzed (n = 182). Differences shown here were confirmed in the Cox multivariate analysis model. (E) OS in intermediate cytogenetic risk group patients.

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