TY - GEN
T1 - Study of population and covariate model in physiologically based pharmacokinetics model used for treatment planning in peptide receptor radionuclide therapy
AU - Riana, Ade
AU - Pawiro, Supriyanto A.
AU - Hardiansyah, Deni
N1 - Publisher Copyright:
© 2021 American Institute of Physics Inc.. All rights reserved.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/3/2
Y1 - 2021/3/2
N2 - 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 [Rk]. The final covariate model of receptor density in the kidney was: [Rk] (10-15mol/l) = 6.32x106∗(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.
AB - 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 [Rk]. The final covariate model of receptor density in the kidney was: [Rk] (10-15mol/l) = 6.32x106∗(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.
UR - http://www.scopus.com/inward/record.url?scp=85102305801&partnerID=8YFLogxK
U2 - 10.1063/5.0037544
DO - 10.1063/5.0037544
M3 - Conference contribution
AN - SCOPUS:85102305801
T3 - AIP Conference Proceedings
BT - 9th National Physics Seminar 2020
A2 - Nasbey, Hadi
A2 - Fahdiran, Riser
A2 - Indrasari, Widyaningrum
A2 - Budi, Esmar
A2 - Bakri, Fauzi
A2 - Prayitno, Teguh Budi
A2 - Muliyati, Dewi
PB - American Institute of Physics Inc.
T2 - 9th National Physics Seminar 2020
Y2 - 20 June 2020
ER -