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Model-informed precision dosing: State of the art and future perspectives
[Display omitted] Model-informed precision dosing (MIPD) stands as a significant development in personalized medicine to tailor drug dosing to individual patient characteristics. MIPD moves beyond traditional therapeutic drug monitoring (TDM) by integrating mathematical predictions of dosing, and co...
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Published in: | Advanced drug delivery reviews 2024-12, Vol.215, p.115421, Article 115421 |
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container_title | Advanced drug delivery reviews |
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creator | Minichmayr, I.K. Dreesen, E. Centanni, M. Wang, Z. Hoffert, Y. Friberg, L.E. Wicha, S.G. |
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Model-informed precision dosing (MIPD) stands as a significant development in personalized medicine to tailor drug dosing to individual patient characteristics. MIPD moves beyond traditional therapeutic drug monitoring (TDM) by integrating mathematical predictions of dosing, and considering patient-specific factors (patient characteristics, drug measurements) as well as different sources of variability. For this purpose, rigorous model qualification is required for the application of MIPD in patients. This review delves into new methods in model selection and validation, also highlighting the role of machine learning in improving MIPD, the utilization of biosensors for real-time monitoring, as well as the potential of models integrating biomarkers for efficacy or toxicity for precision dosing. The clinical evidence of TDM and MIPD is discussed for various medical fields including infection medicine, oncology, transplant medicine, and inflammatory bowel diseases, thereby underscoring the role of pharmacokinetics/pharmacodynamics and specific biomarkers. Further research, particularly randomized clinical trials, is warranted to corroborate the value of MIPD in enhancing patient outcomes and advancing personalized medicine. |
doi_str_mv | 10.1016/j.addr.2024.115421 |
format | article |
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Model-informed precision dosing (MIPD) stands as a significant development in personalized medicine to tailor drug dosing to individual patient characteristics. MIPD moves beyond traditional therapeutic drug monitoring (TDM) by integrating mathematical predictions of dosing, and considering patient-specific factors (patient characteristics, drug measurements) as well as different sources of variability. For this purpose, rigorous model qualification is required for the application of MIPD in patients. This review delves into new methods in model selection and validation, also highlighting the role of machine learning in improving MIPD, the utilization of biosensors for real-time monitoring, as well as the potential of models integrating biomarkers for efficacy or toxicity for precision dosing. The clinical evidence of TDM and MIPD is discussed for various medical fields including infection medicine, oncology, transplant medicine, and inflammatory bowel diseases, thereby underscoring the role of pharmacokinetics/pharmacodynamics and specific biomarkers. Further research, particularly randomized clinical trials, is warranted to corroborate the value of MIPD in enhancing patient outcomes and advancing personalized medicine.</description><identifier>ISSN: 0169-409X</identifier><identifier>ISSN: 1872-8294</identifier><identifier>EISSN: 1872-8294</identifier><identifier>DOI: 10.1016/j.addr.2024.115421</identifier><identifier>PMID: 39159868</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anti-infectives ; Immunosuppression ; Inflammatory bowel disease ; Model-informed precision dosing ; Oncology</subject><ispartof>Advanced drug delivery reviews, 2024-12, Vol.215, p.115421, Article 115421</ispartof><rights>2024 The Author(s)</rights><rights>Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c274t-da934c20f1cad70763b39dbcb3f4b5750978707b44175753de00692cb74ab1b53</cites><orcidid>0000-0002-8773-4845</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39159868$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-544045$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Minichmayr, I.K.</creatorcontrib><creatorcontrib>Dreesen, E.</creatorcontrib><creatorcontrib>Centanni, M.</creatorcontrib><creatorcontrib>Wang, Z.</creatorcontrib><creatorcontrib>Hoffert, Y.</creatorcontrib><creatorcontrib>Friberg, L.E.</creatorcontrib><creatorcontrib>Wicha, S.G.</creatorcontrib><title>Model-informed precision dosing: State of the art and future perspectives</title><title>Advanced drug delivery reviews</title><addtitle>Adv Drug Deliv Rev</addtitle><description>[Display omitted]
Model-informed precision dosing (MIPD) stands as a significant development in personalized medicine to tailor drug dosing to individual patient characteristics. MIPD moves beyond traditional therapeutic drug monitoring (TDM) by integrating mathematical predictions of dosing, and considering patient-specific factors (patient characteristics, drug measurements) as well as different sources of variability. For this purpose, rigorous model qualification is required for the application of MIPD in patients. This review delves into new methods in model selection and validation, also highlighting the role of machine learning in improving MIPD, the utilization of biosensors for real-time monitoring, as well as the potential of models integrating biomarkers for efficacy or toxicity for precision dosing. The clinical evidence of TDM and MIPD is discussed for various medical fields including infection medicine, oncology, transplant medicine, and inflammatory bowel diseases, thereby underscoring the role of pharmacokinetics/pharmacodynamics and specific biomarkers. Further research, particularly randomized clinical trials, is warranted to corroborate the value of MIPD in enhancing patient outcomes and advancing personalized medicine.</description><subject>Anti-infectives</subject><subject>Immunosuppression</subject><subject>Inflammatory bowel disease</subject><subject>Model-informed precision dosing</subject><subject>Oncology</subject><issn>0169-409X</issn><issn>1872-8294</issn><issn>1872-8294</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQQC3UCrbQP8AB-dhDs9iOE8eIC6K0RaLiQEG9Wf6YgFe7cbAdEP--XgU4chrN6M07PIQOKVlSQtvj1VI7F5eMML6ktOGM7qAF7QSrOib5J7QokKw4kf_20JeUVoRQJlqyi_ZqSRvZtd0CXf4JDtaVH_oQN-DwGMH65MOAXUh-uD_BN1lnwKHH-QGwjhnrweF-ylMEPEJMI9jsnyAdoM-9Xif4-jr30e3Pi7_nv6ur61-X52dXlWWC58ppWXPLSE-tdoKItja1dMaauuemEQ2RoitnwzkVZa0dENJKZo3g2lDT1Pvo--xNzzBORo3Rb3R8UUF79cPfnakQ79U0qYZzwrf4txkfY3icIGW18cnCeq0HCFNSNZG8Y7RlrKBsRm0MKUXo392UqG1xtVLb4mpbXM3Fy9PRq38yJeD7y1viApzOAJQoTx6iStbDYMH50jorF_xH_v8sgZEl</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Minichmayr, I.K.</creator><creator>Dreesen, E.</creator><creator>Centanni, M.</creator><creator>Wang, Z.</creator><creator>Hoffert, Y.</creator><creator>Friberg, L.E.</creator><creator>Wicha, S.G.</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-8773-4845</orcidid></search><sort><creationdate>20241201</creationdate><title>Model-informed precision dosing: State of the art and future perspectives</title><author>Minichmayr, I.K. ; Dreesen, E. ; Centanni, M. ; Wang, Z. ; Hoffert, Y. ; Friberg, L.E. ; Wicha, S.G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-da934c20f1cad70763b39dbcb3f4b5750978707b44175753de00692cb74ab1b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anti-infectives</topic><topic>Immunosuppression</topic><topic>Inflammatory bowel disease</topic><topic>Model-informed precision dosing</topic><topic>Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Minichmayr, I.K.</creatorcontrib><creatorcontrib>Dreesen, E.</creatorcontrib><creatorcontrib>Centanni, M.</creatorcontrib><creatorcontrib>Wang, Z.</creatorcontrib><creatorcontrib>Hoffert, Y.</creatorcontrib><creatorcontrib>Friberg, L.E.</creatorcontrib><creatorcontrib>Wicha, S.G.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>Advanced drug delivery reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Minichmayr, I.K.</au><au>Dreesen, E.</au><au>Centanni, M.</au><au>Wang, Z.</au><au>Hoffert, Y.</au><au>Friberg, L.E.</au><au>Wicha, S.G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Model-informed precision dosing: State of the art and future perspectives</atitle><jtitle>Advanced drug delivery reviews</jtitle><addtitle>Adv Drug Deliv Rev</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>215</volume><spage>115421</spage><pages>115421-</pages><artnum>115421</artnum><issn>0169-409X</issn><issn>1872-8294</issn><eissn>1872-8294</eissn><abstract>[Display omitted]
Model-informed precision dosing (MIPD) stands as a significant development in personalized medicine to tailor drug dosing to individual patient characteristics. MIPD moves beyond traditional therapeutic drug monitoring (TDM) by integrating mathematical predictions of dosing, and considering patient-specific factors (patient characteristics, drug measurements) as well as different sources of variability. For this purpose, rigorous model qualification is required for the application of MIPD in patients. This review delves into new methods in model selection and validation, also highlighting the role of machine learning in improving MIPD, the utilization of biosensors for real-time monitoring, as well as the potential of models integrating biomarkers for efficacy or toxicity for precision dosing. The clinical evidence of TDM and MIPD is discussed for various medical fields including infection medicine, oncology, transplant medicine, and inflammatory bowel diseases, thereby underscoring the role of pharmacokinetics/pharmacodynamics and specific biomarkers. Further research, particularly randomized clinical trials, is warranted to corroborate the value of MIPD in enhancing patient outcomes and advancing personalized medicine.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39159868</pmid><doi>10.1016/j.addr.2024.115421</doi><orcidid>https://orcid.org/0000-0002-8773-4845</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anti-infectives Immunosuppression Inflammatory bowel disease Model-informed precision dosing Oncology |
title | Model-informed precision dosing: State of the art and future perspectives |
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