Zhu Jinwei, Zhang Yicui, Zhao Yixin, Zhang Jingwei, Hao Kun, He Hua
State Key Laboratory of Natural Medicines, Jiangsu Province Key Laboratory of Drug Metabolism and Pharmacokinetics, Institute of Pharmaceutical Sciences, China Pharmaceutical University, Nanjing 210009, China.
Center of Drug Metabolism and Pharmacokinetics, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
Pharmaceutics. 2023 Sep 3;15(9):2274. doi: 10.3390/pharmaceutics15092274.
Despite the recent advances in this field, there are limited methods for translating organoid-based study results to clinical response. The goal of this study was to develop a pharmacokinetic/pharmacodynamic (PK/PD) model to facilitate the translation, using oxaliplatin and irinotecan treatments with colorectal cancer (CRC) as examples. The PK models were developed using qualified oxaliplatin and irinotecan PK data from the literature. The PD models were developed based on antitumor efficacy data of SN-38 and oxaliplatin evaluated in vitro using tumor organoids. To predict the clinical response, translational scaling of the models was established by incorporating predicted ultrafiltration platinum in plasma or SN-38 in tumors to PD models as the driver of efficacy. The final PK/PD model can predict PK profiles and responses following treatments with oxaliplatin or irinotecan. After generation of virtual patient cohorts, this model simulated their tumor shrinkages following treatments, which were used in analyzing the efficacies of the two treatments. Consistent with the published clinical trials, the model simulation suggested similar patient responses following the treatments of oxaliplatin and irinotecan with regards to the probabilities of progression-free survival (HR = 1.05, 95%CI [0.97;1.15]) and the objective response rate (OR = 1.15, 95%CI [1.00;1.32]). This proposed translational PK/PD modeling approach provides a significant tool for predicting clinical responses of different agents, which may help decision-making in drug development and guide clinical trial design.
尽管该领域最近取得了进展,但将基于类器官的研究结果转化为临床反应的方法仍然有限。本研究的目的是开发一种药代动力学/药效学(PK/PD)模型以促进这种转化,以奥沙利铂和伊立替康治疗结直肠癌(CRC)为例。PK模型是使用文献中合格的奥沙利铂和伊立替康PK数据开发的。PD模型是基于使用肿瘤类器官在体外评估的SN-38和奥沙利铂的抗肿瘤疗效数据开发的。为了预测临床反应,通过将血浆中预测的超滤铂或肿瘤中的SN-38纳入PD模型作为疗效驱动因素,建立了模型的转化缩放。最终的PK/PD模型可以预测奥沙利铂或伊立替康治疗后的PK概况和反应。生成虚拟患者队列后,该模型模拟了他们治疗后的肿瘤缩小情况,用于分析两种治疗的疗效。与已发表的临床试验一致,模型模拟表明奥沙利铂和伊立替康治疗后患者的反应在无进展生存概率(HR = 1.05,95%CI [0.97;1.15])和客观缓解率(OR = 1.15,95%CI [1.00;1.32])方面相似。这种提出的转化PK/PD建模方法为预测不同药物的临床反应提供了一个重要工具,这可能有助于药物开发中的决策制定并指导临床试验设计。