Application of physiologically based pharmacokinetic modeling to understand real-world outcomes in patients receiving imatinib for chronic myeloid leukemia

We aimed to use physiologically based pharmacokinetic (PBPK) modeling and simulation to predict imatinib steady-state plasma exposure in patients with chronic myeloid leukemia (CML) to investigate variability in outcomes. A validated imatinib PBPK model (Simcyp Simulator) was used to predict imatinib AUC(ss), C-ss,C-min and C-ss,C-max for patients with CML (n = 68) from a real-world retrospective observational study. Differences in imatinib exposure were evaluated based on clinical outcomes, (a) Early Molecular Response (EMR) achievement and (b) occurrence of grade & GE;3 adverse drug reactions (ADRs), using the Kruskal-Wallis rank sum test. Sensitivity analyses explored the influence of patient characteristics and drug interactions on imatinib exposure. Simulated imatinib exposure was significantly higher in patients who achieved EMR compared to patients who did not (geometric mean AUC(0-24,ss) 51.2 vs. 42.7 & mu;g h mL(-1), p < 0.05; C-ss,C-min 1.1 vs. 0.9 & mu;g mL(-1), p < 0.05; C-ss,C-max 3.4 vs. 2.8 & mu;g mL(-1), p < 0.05). Patients who experienced grade & GE;3 ADRs had a significantly higher simulated imatinib exposure compared to patients who did not (AUC(0-24,ss) 56.1 vs. 45.9 & mu;g h mL(-1), p < 0.05; C-ss,C-min 1.2 vs. 1.0 & mu;g mL(-1), p < 0.05; C-ss,C-max 3.7 vs. 3.0 & mu;g mL(-1), p < 0.05). Simulations identified a range of patient (sex, age, weight, abundance of hepatic CYP2C8 and CYP3A4, & alpha;(1)-acid glycoprotein concentrations, liver and kidney function) and medication-related factors (dose, concomitant CYP2C8 modulators) contributing to the inter-individual variability in imatinib exposure. Relationships between imatinib plasma exposure, EMR achievement and ADRs support the rationale for therapeutic drug monitoring to guide imatinib dosing to achieve optimal outcomes in CML.