Literature DB >> 33253425

Tacrolimus Exposure Prediction Using Machine Learning.

Jean-Baptiste Woillard1,2,3, Marc Labriffe1,2,3, Jean Debord1,2,3, Pierre Marquet1,2,3.   

Abstract

The aim of this work is to estimate the area-under the blood concentration curve of tacrolimus (TAC) following b.i.d. or q.d. dosing in organ transplant patients, using Xgboost machine learning (ML) models. A total of 4,997 and 1,452 TAC interdose area under the curves (AUCs) from patients on b.i.d. and q.d. TAC, sent to our Immunosuppressant Bayesian Dose Adjustment expert system (www.pharmaco.chu-limoges.fr/) for AUC estimation and dose recommendation based on TAC concentrations measured at least at 3 sampling times (predose, ~ 1 and 3 hours after dosing) were used to develop 4 ML models based on 2 or 3 concentrations. For each model, data splitting was performed to obtain a training set (75%) and a test set (25%). The Xgboost models in the training set with the lowest root mean square error (RMSE) in a 10-fold cross-validation experiment were evaluated in the test set and in 6 independent full-pharmacokinetic (PK) datasets from renal, liver, and heart transplant patients. ML models based on two or three concentrations, differences between these concentrations, relative deviations from theoretical times of sampling, and four covariates (dose, type of transplantation, age, and time between transplantation and sampling) yielded excellent AUC estimation performance in the test datasets (relative bias < 5% and relative RMSE < 10%) and better performance than maximum a posteriori Bayesian estimation in the six independent full-PK datasets. The Xgboost ML models described allow accurate estimation of TAC interdose AUC and can be used for routine TAC exposure estimation and dose adjustment. They will soon be implemented in a dedicated web interface.
© 2020 The Authors Clinical Pharmacology & Therapeutics © 2020 American Society for Clinical Pharmacology and Therapeutics.

Entities:  

Year:  2021        PMID: 33253425     DOI: 10.1002/cpt.2123

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  6 in total

1.  Application of Machine Learning Classification to Improve the Performance of Vancomycin Therapeutic Drug Monitoring.

Authors:  Sooyoung Lee; Moonsik Song; Jongdae Han; Donghwan Lee; Bo-Hyung Kim
Journal:  Pharmaceutics       Date:  2022-05-09       Impact factor: 6.525

2.  Construction and Interpretation of Prediction Model of Teicoplanin Trough Concentration via Machine Learning.

Authors:  Pan Ma; Ruixiang Liu; Wenrui Gu; Qing Dai; Yu Gan; Jing Cen; Shenglan Shang; Fang Liu; Yongchuan Chen
Journal:  Front Med (Lausanne)       Date:  2022-03-08

3.  Machine learning algorithms to estimate everolimus exposure trained on simulated and patient pharmacokinetic profiles.

Authors:  Marc Labriffe; Jean-Baptiste Woillard; Jean Debord; Pierre Marquet
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2022-05-22

4.  Machine Learning and Pharmacometrics for Prediction of Pharmacokinetic Data: Differences, Similarities and Challenges Illustrated with Rifampicin.

Authors:  Lina Keutzer; Huifang You; Ali Farnoud; Joakim Nyberg; Sebastian G Wicha; Gareth Maher-Edwards; Georgios Vlasakakis; Gita Khalili Moghaddam; Elin M Svensson; Michael P Menden; Ulrika S H Simonsson
Journal:  Pharmaceutics       Date:  2022-07-22       Impact factor: 6.525

5.  Editorial: Therapeutic Drug Monitoring in Solid Organ Transplantation.

Authors:  Christine E Staatz; Nicole M Isbel; Troels K Bergmann; Bente Jespersen; Niels Henrik Buus
Journal:  Front Pharmacol       Date:  2021-12-10       Impact factor: 5.810

6.  A hybrid machine learning/pharmacokinetic approach outperforms maximum a posteriori Bayesian estimation by selectively flattening model priors.

Authors:  Jasmine H Hughes; Ron J Keizer
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2021-07-26
  6 in total

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