Figure 1.
Figure 1. Prognostic value of frequencies of CD34+CD38− putative LSC (pLSC) compartment at follow-up. The Kaplan-Meier analyses for RFS for the CD34+CD38− pLSC compartment at follow-up for 3 consecutive therapy cycles are shown. The optimal cutoff levels were chosen to define high pLSC frequency (pLSC+) and low pLSC frequency (pLSC−) after first induction cycle (0.0003%, which is 3 pLSCs in 1 000 000 WBCs) and after second induction cycle and consolidation therapy (0.0001%, 1 pLSC in 1 000 000 WBCs). After the first induction cycle (A, 71 patients), second induction cycle (B, 77 patients), and after consolidation therapy (C, 48 patients), pLSC+ patients showed significantly poorer outcome as compared with pLSC− patients.

Prognostic value of frequencies of CD34+CD38 putative LSC (pLSC) compartment at follow-up. The Kaplan-Meier analyses for RFS for the CD34+CD38 pLSC compartment at follow-up for 3 consecutive therapy cycles are shown. The optimal cutoff levels were chosen to define high pLSC frequency (pLSC+) and low pLSC frequency (pLSC) after first induction cycle (0.0003%, which is 3 pLSCs in 1 000 000 WBCs) and after second induction cycle and consolidation therapy (0.0001%, 1 pLSC in 1 000 000 WBCs). After the first induction cycle (A, 71 patients), second induction cycle (B, 77 patients), and after consolidation therapy (C, 48 patients), pLSC+ patients showed significantly poorer outcome as compared with pLSC patients.

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