Figure 1.
Figure 1. Cumulative incidence of relapse. (A) Incidence of relapse by TCR status. Cumulative incidence of relapse is indicated in the 23, 29, and 29 CR patients with IM (solid line), pre-αβ (bold dotted line), and TCR+ ALL (thin dotted line), respectively. No significant difference was observed between these 3 subsets (P = .51 by the Gray test). (B) Incidence of relapse by genetic abnormalities. Cumulative incidence of relapse was higher in the 11 CR patients with SIL-TAL1+ ALL (thin dotted line; 82% at 4 years) and in the 6 CR patients with HOX11L2+ ALL (bold dotted line; 83% at 4 years) compared with the 54 other CR patients tested (solid line; 53% at 4 years) (P = .05 by the Gray test).

Cumulative incidence of relapse. (A) Incidence of relapse by TCR status. Cumulative incidence of relapse is indicated in the 23, 29, and 29 CR patients with IM (solid line), pre-αβ (bold dotted line), and TCR+ ALL (thin dotted line), respectively. No significant difference was observed between these 3 subsets (P = .51 by the Gray test). (B) Incidence of relapse by genetic abnormalities. Cumulative incidence of relapse was higher in the 11 CR patients with SIL-TAL1+ ALL (thin dotted line; 82% at 4 years) and in the 6 CR patients with HOX11L2+ ALL (bold dotted line; 83% at 4 years) compared with the 54 other CR patients tested (solid line; 53% at 4 years) (P = .05 by the Gray test).

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