075: Population Pharmacokinetics of Trastuzumab Deruxtecan (T-DXd) in Subjects With HER2-mutant & HER2-overexpressing Non-Small Cell Lung Cancer (NSCLC)

Statement of Purpose, Innovation or Hypothesis: T-DXd is a novel human epidermal growth factor receptor 2 (HER2) targeting antibody drug conjugate, approved globally at the dose of 5.4 mg/kg in HER2-positive or HER2-low breast cancer (BC) and HER2-mutant (HER2m) NSCLC^1,2. The aim of the analysis was to characterize the populaton pharmacokinetics (PopPK) of T-DXd and its released payload, DXd, in HER2m or HER2-overexpressing (HER2-OE) NSCLC subjects using data across tumor types (BC, NSCLC and others) from 12 Phase 1 to 3 studies with T-DXd doses ranging from 0.8-8.0 mg/kg.

Description of Methods & Materials: Analysis was performed using nonlinear mixed-effects modeling methods in NONMEM® (version 7.4.3), similar to the previous analysis in HER2-positive BC [1]. Covariate effects were explored on the PK parameters of T-DXd and DXd.

Data & Results: Analysis included data across 1822 subjects, including 346, 1128, and 348 subjects with NSCLC, BC, and other cancers, respectively. The PK of T-DXd and DXd were adequately described by a PopPK model, judging by standard model diagnostics³. Covariate effects on T-DXd and DXd steady-state area under the concentration-time curve (AUC) were not clinically meaningful (within 0.8 to 1.25 AUC ratio interval for tested covariate level versus reference), except for subjects with high body weight (e.g., 90 kg; 95th percentile) showing a 31% and 37% higher T-DXd and DXd AUC, respectively, relative to typical subject with 58 kg body weight (median). The T-DXd and DXd AUC were also similar across subjects with BC, HER2m or HER2-OE NSCLC, with the same T-DXd dose. T-DXd and DXd AUC in NSCLC subjects were similar across subjects with mild hepatic or mild or moderate renal impairment (vs. normal counterparts), region (Asia, North America, Europe, and rest of the world), and race-country (Asian-Japan, Asian-Non-Japan, and Non-Asian) groups.

Interpretation, Conclusion or Significance: T-DXd and DXd exposures were similar across subjects with BC and HER2m or HER2-OE NSCLC, as well as across hepatic function, renal function, region, and race-country groups within NSCLC supporting the use of 5.4 mg/kg dose (approved dose in BC) in HER2m or HER2-OE NSCLC from PK perspective.

Disclosures: Amit Khatri, Tushar Garimella and Malaz Abutarif are employees of Daiichi Sankyo Inc. Enoch Cobbina is a former employee of Daiichi Sankyo Inc.

Citations/References: 1. Enhertu [package insert]. Basking Ridge, NJ: Daiichi Sankyo, Inc.; 2022. 2. Enhertu [summary of product characteristics]. Daiichi Sankyo Europe GmbH, Munich; 2022. 3. Yin O et al. Clin Pharmacol Ther. 2021;109(5):1314-1325.

Additional Information/Authors: NA