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Study of population and covariate model in physiologically based pharmacokinetics model used for treatment planning in peptide receptor radionuclide therapy

机译:肽受体放射性核素治疗治疗计划的生理基于药代动力学模型的人口与协变化模型研究

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In this study, we implemented for the first time the Population and Covariate Model (POPCOV) to simplify the Individual Treatment Planning (ITP) process in PRRT with minimal Physiologically based Pharmacokinetic (mPBPK) model. POPCOV method was used to predict the unknown parameters of the PBPK model using the individual covariates. Stepwise selection procedures (forward selection and backward elimination) were used for the covariate selection and the derivation of the final model. The performance of the final model was tested by comparing the predicted time-integrated activity coefficient (TIACs) from the Fixed-Dose Treatment Planning (FDP) i.e., mPBPK with mean parameters, and conventional ITP method, i.e., mPBPK with individual estimated parameters. Based on the POPCOV analysis, GFR was identified as the best covariate for the receptor density in the kidneys [R_k]. The final covariate model of receptor density in the kidney was: [R_k] (10~(-15)mol/l)=6.32×10~(6*)(GFR/0.09)~(0.67). These results indicated that the performance of POPCOV for ITP was around 12% better than the FDP and around 26% worse than the conventional ITP method for the kidneys. The results showed that the POPCOV method could be used as an alternative method in PRRT to predict kidneys TIACs in a case where the individual biokinetic data is unavailable.
机译:在这项研究中,我们首次实施了人口和协变量模型(POPCOV),以简化PRRT中的个体治疗计划(ITP)过程,以最小的生理基础的药代动力学(MPBPK)模型。 Popcov方法用于预测使用单个协变量的PBPK模型的未知参数。逐步选择程序(正向选择和后退消除)用于协变量选择和最终模型的推导。通过将预测的时间综合活性系数(TIACS)与来自固定剂量治疗计划(FDP)I.,MPBPK具有平均参数的MPBPK,以及具有单个估计参数的MPBPK来测试最终模型的性能。基于POPCOV分析,GFR被鉴定为肾脏受体密度的最佳变性[R_K]。肾脏中受体密度的最终协变化模型是:[R_K](10〜(-15)mol / l)= 6.32×10〜(6 *)(GFR / 0.09)〜(0.67)。这些结果表明,Popcov的ITP的性能比FDP更好的12%,比肾脏的常规ITP方法差约26%。结果表明,POPCOV方法可以用作PRRT中的替代方法,以预测各个杀虫数据不可用的情况下的肾脏TIAC。

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