Clinical Pharmacology & Therapeutics · 2018 · 38 citations · 35 references
MedicineOncologyPharmacologyCancer PharmacologyMedical OncologyPharmacokinetics Of Anticancer AgentsBiomarker ModelingCancer BiomarkersOncology PharmacologyPharmacodynamics Of Anticancer AgentsPharmacodynamics Of Anticancer DrugsPharmacokinetics Of Anticancer DrugsAtezolizumab TherapyBiomarkersCirculating BiomarkersCirculating Tumor BiomarkersNon-small Cell Lung Cancer TherapyProgrammed Death-ligand 1 BiomarkerTumor Response PredictionTumor Shrinkage Assessment
To assess circulating biomarkers as predictors of antitumor response to atezolizumab (anti‐programmed death‐ligand 1 (PD‐L1), Tecentriq) serum pharmacokinetic ( PK ) and 95 plasma biomarkers were analyzed in 88 patients with relapsed/refractory non‐small cell lung cancer ( NSCLC ) receiving atezolizumab i.v. q3w (10–20 mg/kg) in the PCD4989g phase I clinical trial. Following exploratory analyses, two plasma biomarkers were chosen for further study and correlation with change in tumor size (the sum of the longest diameter) was assessed in a pharmacokinetic/pharmacodynamic ( PK/PD ) tumor modeling framework. When longitudinal kinetics of biomarkers and tumor size were modeled, tumor shrinkage was found to significantly correlate with area under the curve ( AUC ), baseline factors (metastatic sites, liver metastases, and smoking status), and relative change in interleukin (IL)‐18 level from baseline at day 21 ( RCFB IL ‐18,d21 ). Although AUC was a major predictor of tumor shrinkage, the effect was estimated to dissipate with an average half‐life of 80 days, whereas RCFB IL ‐18,d21 seemed relevant to the duration of the response.
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