Loading…
Individualization of Drug Therapy: History, Present State, and Opportunities for the Future
Individualization of drug therapy, described as tailoring drug selection and drug dosing to a given patient, has been an objective of physicians and other health‐care providers for centuries. An understanding of the pathogenesis of the disease, the mechanism of action of the drug, and exposure–respo...
Saved in:
Published in: | Clinical pharmacology and therapeutics 2012-10, Vol.92 (4), p.458-466 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83 |
---|---|
cites | cdi_FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83 |
container_end_page | 466 |
container_issue | 4 |
container_start_page | 458 |
container_title | Clinical pharmacology and therapeutics |
container_volume | 92 |
creator | Lesko, L J Schmidt, S |
description | Individualization of drug therapy, described as tailoring drug selection and drug dosing to a given patient, has been an objective of physicians and other health‐care providers for centuries. An understanding of the pathogenesis of the disease, the mechanism of action of the drug, and exposure–response relationships provides the framework for individualization. There are many approaches to individualization: selecting an antibiotic based on minimum effective concentrations and bacterial sensitivity, population (sparse sample) pharmacokinetics, therapeutic drug monitoring and, more recently, pharmacogenomics. The goal of individualization is to optimize the efficacy of a drug, minimize its toxicity, or both. With the growth of technology and databases, drug–disease–trial models and simulation have become useful for integrating information from many different domains. Physiology‐based pharmacokinetic (PBPK) models have provided a mechanistic approach to individualization, and clinical trial designs such as those involving enrichment have also enabled individualization. In the future, “‐omics” technologies, vaccines, ex vivo gene therapy, and the so‐called “diseases‐in‐a‐dish” will provide additional strategies to achieve individualization.
Clinical Pharmacology & Therapeutics (2012); 92 4, 458–466. doi:10.1038/clpt.2012.113 |
doi_str_mv | 10.1038/clpt.2012.113 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1038_clpt_2012_113</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CPTCLPT2012113</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83</originalsourceid><addsrcrecordid>eNp9kM1Kw0AYRQdRbK0u3co8QFPnL8mMO6n2B4ItGHDhYpgkEzvaJmEyUePTm5LapauPC-dePg4A1xhNMKL8Nt1WbkIQJhOM6QkYYp8SL_CpfwqGCCHhCUKDAbio6_cuMsH5ORgQIhjnAg_B67LIzKfJGrU1P8qZsoBlDh9s8wbjjbaqau_gwtSutO0Yrq2udeHgs1NOj6EqMriqqtK6pjDO6BrmpYVuo-GscY3Vl-AsV9taXx3uCMSzx3i68KLVfDm9j7yUsZB6qUKZTpI8JAmhnHGlcZJileEcYaopU4wgRnPFdBL4AjMiklBhjoJUED_ldAS8fja1ZV1bncvKmp2yrcRI7h3JvSO5dyQ7Rx1_0_NVk-x0dqT_pHSA6IEvs9Xt_2tyuo6n0Tre53788EznTH8fu8p-yCCkoS9fnuZyHc6Zz6JYcvoLJjWD4Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Individualization of Drug Therapy: History, Present State, and Opportunities for the Future</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Lesko, L J ; Schmidt, S</creator><creatorcontrib>Lesko, L J ; Schmidt, S</creatorcontrib><description>Individualization of drug therapy, described as tailoring drug selection and drug dosing to a given patient, has been an objective of physicians and other health‐care providers for centuries. An understanding of the pathogenesis of the disease, the mechanism of action of the drug, and exposure–response relationships provides the framework for individualization. There are many approaches to individualization: selecting an antibiotic based on minimum effective concentrations and bacterial sensitivity, population (sparse sample) pharmacokinetics, therapeutic drug monitoring and, more recently, pharmacogenomics. The goal of individualization is to optimize the efficacy of a drug, minimize its toxicity, or both. With the growth of technology and databases, drug–disease–trial models and simulation have become useful for integrating information from many different domains. Physiology‐based pharmacokinetic (PBPK) models have provided a mechanistic approach to individualization, and clinical trial designs such as those involving enrichment have also enabled individualization. In the future, “‐omics” technologies, vaccines, ex vivo gene therapy, and the so‐called “diseases‐in‐a‐dish” will provide additional strategies to achieve individualization.
Clinical Pharmacology & Therapeutics (2012); 92 4, 458–466. doi:10.1038/clpt.2012.113</description><identifier>ISSN: 0009-9236</identifier><identifier>EISSN: 1532-6535</identifier><identifier>DOI: 10.1038/clpt.2012.113</identifier><identifier>PMID: 22948891</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Drug Monitoring - methods ; Drug Monitoring - trends ; Forecasting ; Humans ; Pharmaceutical Preparations - administration & dosage ; Pharmaceutical Preparations - metabolism ; Pharmacogenetics - methods ; Pharmacogenetics - trends ; Precision Medicine - methods ; Precision Medicine - trends</subject><ispartof>Clinical pharmacology and therapeutics, 2012-10, Vol.92 (4), p.458-466</ispartof><rights>2012 American Society for Clinical Pharmacology and Therapeutics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83</citedby><cites>FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22948891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lesko, L J</creatorcontrib><creatorcontrib>Schmidt, S</creatorcontrib><title>Individualization of Drug Therapy: History, Present State, and Opportunities for the Future</title><title>Clinical pharmacology and therapeutics</title><addtitle>Clinical Pharmacology & Therapeutics</addtitle><description>Individualization of drug therapy, described as tailoring drug selection and drug dosing to a given patient, has been an objective of physicians and other health‐care providers for centuries. An understanding of the pathogenesis of the disease, the mechanism of action of the drug, and exposure–response relationships provides the framework for individualization. There are many approaches to individualization: selecting an antibiotic based on minimum effective concentrations and bacterial sensitivity, population (sparse sample) pharmacokinetics, therapeutic drug monitoring and, more recently, pharmacogenomics. The goal of individualization is to optimize the efficacy of a drug, minimize its toxicity, or both. With the growth of technology and databases, drug–disease–trial models and simulation have become useful for integrating information from many different domains. Physiology‐based pharmacokinetic (PBPK) models have provided a mechanistic approach to individualization, and clinical trial designs such as those involving enrichment have also enabled individualization. In the future, “‐omics” technologies, vaccines, ex vivo gene therapy, and the so‐called “diseases‐in‐a‐dish” will provide additional strategies to achieve individualization.
Clinical Pharmacology & Therapeutics (2012); 92 4, 458–466. doi:10.1038/clpt.2012.113</description><subject>Drug Monitoring - methods</subject><subject>Drug Monitoring - trends</subject><subject>Forecasting</subject><subject>Humans</subject><subject>Pharmaceutical Preparations - administration & dosage</subject><subject>Pharmaceutical Preparations - metabolism</subject><subject>Pharmacogenetics - methods</subject><subject>Pharmacogenetics - trends</subject><subject>Precision Medicine - methods</subject><subject>Precision Medicine - trends</subject><issn>0009-9236</issn><issn>1532-6535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kM1Kw0AYRQdRbK0u3co8QFPnL8mMO6n2B4ItGHDhYpgkEzvaJmEyUePTm5LapauPC-dePg4A1xhNMKL8Nt1WbkIQJhOM6QkYYp8SL_CpfwqGCCHhCUKDAbio6_cuMsH5ORgQIhjnAg_B67LIzKfJGrU1P8qZsoBlDh9s8wbjjbaqau_gwtSutO0Yrq2udeHgs1NOj6EqMriqqtK6pjDO6BrmpYVuo-GscY3Vl-AsV9taXx3uCMSzx3i68KLVfDm9j7yUsZB6qUKZTpI8JAmhnHGlcZJileEcYaopU4wgRnPFdBL4AjMiklBhjoJUED_ldAS8fja1ZV1bncvKmp2yrcRI7h3JvSO5dyQ7Rx1_0_NVk-x0dqT_pHSA6IEvs9Xt_2tyuo6n0Tre53788EznTH8fu8p-yCCkoS9fnuZyHc6Zz6JYcvoLJjWD4Q</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Lesko, L J</creator><creator>Schmidt, S</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201210</creationdate><title>Individualization of Drug Therapy: History, Present State, and Opportunities for the Future</title><author>Lesko, L J ; Schmidt, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Drug Monitoring - methods</topic><topic>Drug Monitoring - trends</topic><topic>Forecasting</topic><topic>Humans</topic><topic>Pharmaceutical Preparations - administration & dosage</topic><topic>Pharmaceutical Preparations - metabolism</topic><topic>Pharmacogenetics - methods</topic><topic>Pharmacogenetics - trends</topic><topic>Precision Medicine - methods</topic><topic>Precision Medicine - trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lesko, L J</creatorcontrib><creatorcontrib>Schmidt, S</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Clinical pharmacology and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lesko, L J</au><au>Schmidt, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Individualization of Drug Therapy: History, Present State, and Opportunities for the Future</atitle><jtitle>Clinical pharmacology and therapeutics</jtitle><addtitle>Clinical Pharmacology & Therapeutics</addtitle><date>2012-10</date><risdate>2012</risdate><volume>92</volume><issue>4</issue><spage>458</spage><epage>466</epage><pages>458-466</pages><issn>0009-9236</issn><eissn>1532-6535</eissn><abstract>Individualization of drug therapy, described as tailoring drug selection and drug dosing to a given patient, has been an objective of physicians and other health‐care providers for centuries. An understanding of the pathogenesis of the disease, the mechanism of action of the drug, and exposure–response relationships provides the framework for individualization. There are many approaches to individualization: selecting an antibiotic based on minimum effective concentrations and bacterial sensitivity, population (sparse sample) pharmacokinetics, therapeutic drug monitoring and, more recently, pharmacogenomics. The goal of individualization is to optimize the efficacy of a drug, minimize its toxicity, or both. With the growth of technology and databases, drug–disease–trial models and simulation have become useful for integrating information from many different domains. Physiology‐based pharmacokinetic (PBPK) models have provided a mechanistic approach to individualization, and clinical trial designs such as those involving enrichment have also enabled individualization. In the future, “‐omics” technologies, vaccines, ex vivo gene therapy, and the so‐called “diseases‐in‐a‐dish” will provide additional strategies to achieve individualization.
Clinical Pharmacology & Therapeutics (2012); 92 4, 458–466. doi:10.1038/clpt.2012.113</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>22948891</pmid><doi>10.1038/clpt.2012.113</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-9236 |
ispartof | Clinical pharmacology and therapeutics, 2012-10, Vol.92 (4), p.458-466 |
issn | 0009-9236 1532-6535 |
language | eng |
recordid | cdi_crossref_primary_10_1038_clpt_2012_113 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Drug Monitoring - methods Drug Monitoring - trends Forecasting Humans Pharmaceutical Preparations - administration & dosage Pharmaceutical Preparations - metabolism Pharmacogenetics - methods Pharmacogenetics - trends Precision Medicine - methods Precision Medicine - trends |
title | Individualization of Drug Therapy: History, Present State, and Opportunities for the Future |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T11%3A45%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Individualization%20of%20Drug%20Therapy:%20History,%20Present%20State,%20and%20Opportunities%20for%20the%20Future&rft.jtitle=Clinical%20pharmacology%20and%20therapeutics&rft.au=Lesko,%20L%20J&rft.date=2012-10&rft.volume=92&rft.issue=4&rft.spage=458&rft.epage=466&rft.pages=458-466&rft.issn=0009-9236&rft.eissn=1532-6535&rft_id=info:doi/10.1038/clpt.2012.113&rft_dat=%3Cwiley_cross%3ECPTCLPT2012113%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4473-ca0debbf72b23848ae1bc1ad1f013e34a42043fa4eb6591429b7a1806c925c83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/22948891&rfr_iscdi=true |