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A PK/PD Analysis of Circulating Biomarkers and Their Relationship to Tumor Response in Atezolizumab‐Treated non‐small Cell Lung Cancer Patients

机译:接受Atezolizumab治疗的非小细胞肺癌患者循环生物标志物的PK / PD分析及其与肿瘤反应的关系

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摘要

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 (RCFBIL ‐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 RCFBIL ‐18,d21 seemed relevant to the duration of the response.
机译:为了评估循环生物标志物作为抗Atezolizumab(抗程序性死亡配体1(PD-L1),Tecentriq)抗肿瘤反应的预测指标,对88例复发/难治性非小细胞肺癌患者的血清药代动力学(PK)和95种血浆生物标志物进行了分析静脉接受阿特珠单抗治疗的癌症(NSCLC) PCD4989g I期临床试验的q3w(10–20 mg / kg)。在进行探索性分析之后,选择了两种血浆生物标记物进行进一步研究,并在药代动力学/药效学(PK / PD)肿瘤建模框架中评估了与肿瘤大小变化(最长直径的总和)的相关性。当对生物标志物的纵向动力学和肿瘤大小进行建模时,发现肿瘤缩小与曲线下面积(AUC),基线因素(转移部位,肝转移和吸烟状态)以及白介素(IL)的相对变化显着相关-从第21天的基线起18水平(RCFBIL‐18,d21)。尽管AUC是肿瘤缩小的主要预测因子,但估计其消失的平均半衰期为80天,而RCFBIL-18,d21似乎与反应持续时间有关。

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