Figure 4
Figure 4. Correlation between mitochondrial priming and in vivo response in the PB, lymph node, and BM compartments. (A) Lymphocyte response. Correlation between percentage reduction in the absolute lymphocyte count at 6 weeks in CLL patients on the M12-175 trial and mitochondrial priming, as assessed by percentage cytochrome C loss after exposure of CLL cells (mean viability after thawing 92% [range 80% to 98%]) to BIM BH3 peptide at 0.8 μM (P = .05, R2 = 0.23), in 13 evaluable patients with lymphocytosis at study entry. (B) Nodal response. Correlations between percentage reductions in the SPD of target lymph nodes at 6 weeks and mitochondrial priming (P = .19, R2 = 0.14) in 14 evaluable patients. (C) Marrow response. Correlation between percentage reduction in CLL cell BM infiltrate at first restaging at approximately week 24 and mitochondrial priming (P = .01, R2 = 0.63) in 9 evaluable patients.

Correlation between mitochondrial priming and in vivo response in the PB, lymph node, and BM compartments. (A) Lymphocyte response. Correlation between percentage reduction in the absolute lymphocyte count at 6 weeks in CLL patients on the M12-175 trial and mitochondrial priming, as assessed by percentage cytochrome C loss after exposure of CLL cells (mean viability after thawing 92% [range 80% to 98%]) to BIM BH3 peptide at 0.8 μM (P = .05, R2 = 0.23), in 13 evaluable patients with lymphocytosis at study entry. (B) Nodal response. Correlations between percentage reductions in the SPD of target lymph nodes at 6 weeks and mitochondrial priming (P = .19, R2 = 0.14) in 14 evaluable patients. (C) Marrow response. Correlation between percentage reduction in CLL cell BM infiltrate at first restaging at approximately week 24 and mitochondrial priming (P = .01, R2 = 0.63) in 9 evaluable patients.

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