The Personalized Advantage Index: translating research on prediction into individualized treatment recommendations. A demonstration
Advances in personalized medicine require the identification of variables that predict differential response to treatments as well as the development and refinement of methods to transform predictive information into actionable recommendations. To illustrate and test a new method for integrating pre...
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creator | DeRubeis, Robert J Cohen, Zachary D Forand, Nicholas R Fournier, Jay C Gelfand, Lois A Lorenzo-Luaces, Lorenzo |
description | Advances in personalized medicine require the identification of variables that predict differential response to treatments as well as the development and refinement of methods to transform predictive information into actionable recommendations.
To illustrate and test a new method for integrating predictive information to aid in treatment selection, using data from a randomized treatment comparison.
Data from a trial of antidepressant medications (N = 104) versus cognitive behavioral therapy (N = 50) for Major Depressive Disorder were used to produce predictions of post-treatment scores on the Hamilton Rating Scale for Depression (HRSD) in each of the two treatments for each of the 154 patients. The patient's own data were not used in the models that yielded these predictions. Five pre-randomization variables that predicted differential response (marital status, employment status, life events, comorbid personality disorder, and prior medication trials) were included in regression models, permitting the calculation of each patient's Personalized Advantage Index (PAI), in HRSD units.
For 60% of the sample a clinically meaningful advantage (PAI≥3) was predicted for one of the treatments, relative to the other. When these patients were divided into those randomly assigned to their "Optimal" treatment versus those assigned to their "Non-optimal" treatment, outcomes in the former group were superior (d = 0.58, 95% CI .17-1.01).
This approach to treatment selection, implemented in the context of two equally effective treatments, yielded effects that, if obtained prospectively, would rival those routinely observed in comparisons of active versus control treatments. |
doi_str_mv | 10.1371/journal.pone.0083875 |
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To illustrate and test a new method for integrating predictive information to aid in treatment selection, using data from a randomized treatment comparison.
Data from a trial of antidepressant medications (N = 104) versus cognitive behavioral therapy (N = 50) for Major Depressive Disorder were used to produce predictions of post-treatment scores on the Hamilton Rating Scale for Depression (HRSD) in each of the two treatments for each of the 154 patients. The patient's own data were not used in the models that yielded these predictions. Five pre-randomization variables that predicted differential response (marital status, employment status, life events, comorbid personality disorder, and prior medication trials) were included in regression models, permitting the calculation of each patient's Personalized Advantage Index (PAI), in HRSD units.
For 60% of the sample a clinically meaningful advantage (PAI≥3) was predicted for one of the treatments, relative to the other. When these patients were divided into those randomly assigned to their "Optimal" treatment versus those assigned to their "Non-optimal" treatment, outcomes in the former group were superior (d = 0.58, 95% CI .17-1.01).
This approach to treatment selection, implemented in the context of two equally effective treatments, yielded effects that, if obtained prospectively, would rival those routinely observed in comparisons of active versus control treatments.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0083875</identifier><identifier>PMID: 24416178</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Active control ; Analysis ; Antidepressants ; Antidepressive Agents - therapeutic use ; Behavior modification ; Behavioral medicine ; Care and treatment ; Clinical outcomes ; Clinical trials ; Cognitive ability ; Cognitive behavioral therapy ; Cognitive Therapy ; Comorbidity ; Depression (Mood disorder) ; Depressive Disorder, Major - drug therapy ; Drugs ; Health Planning Guidelines ; Humans ; Medical imaging ; Medicine ; Mental depression ; Mental health ; Patients ; Polyamide-imides ; Precision Medicine ; Predictions ; Prognosis ; Psychiatric Status Rating Scales ; Psychiatry ; Psychology ; Randomization ; Regression analysis ; Regression models ; Researchers ; Social and Behavioral Sciences ; Test procedures ; Translational Medical Research</subject><ispartof>PloS one, 2014-01, Vol.9 (1), p.e83875</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 DeRubeis et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 DeRubeis et al 2014 DeRubeis et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-2ef4fdabb4ae5cabaa35164f550278b8d5322aab5a0841b11527da40e1e1c44d3</citedby><cites>FETCH-LOGICAL-c692t-2ef4fdabb4ae5cabaa35164f550278b8d5322aab5a0841b11527da40e1e1c44d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885521/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885521/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24416178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DeRubeis, Robert J</creatorcontrib><creatorcontrib>Cohen, Zachary D</creatorcontrib><creatorcontrib>Forand, Nicholas R</creatorcontrib><creatorcontrib>Fournier, Jay C</creatorcontrib><creatorcontrib>Gelfand, Lois A</creatorcontrib><creatorcontrib>Lorenzo-Luaces, Lorenzo</creatorcontrib><title>The Personalized Advantage Index: translating research on prediction into individualized treatment recommendations. A demonstration</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Advances in personalized medicine require the identification of variables that predict differential response to treatments as well as the development and refinement of methods to transform predictive information into actionable recommendations.
To illustrate and test a new method for integrating predictive information to aid in treatment selection, using data from a randomized treatment comparison.
Data from a trial of antidepressant medications (N = 104) versus cognitive behavioral therapy (N = 50) for Major Depressive Disorder were used to produce predictions of post-treatment scores on the Hamilton Rating Scale for Depression (HRSD) in each of the two treatments for each of the 154 patients. The patient's own data were not used in the models that yielded these predictions. Five pre-randomization variables that predicted differential response (marital status, employment status, life events, comorbid personality disorder, and prior medication trials) were included in regression models, permitting the calculation of each patient's Personalized Advantage Index (PAI), in HRSD units.
For 60% of the sample a clinically meaningful advantage (PAI≥3) was predicted for one of the treatments, relative to the other. When these patients were divided into those randomly assigned to their "Optimal" treatment versus those assigned to their "Non-optimal" treatment, outcomes in the former group were superior (d = 0.58, 95% CI .17-1.01).
This approach to treatment selection, implemented in the context of two equally effective treatments, yielded effects that, if obtained prospectively, would rival those routinely observed in comparisons of active versus control treatments.</description><subject>Active control</subject><subject>Analysis</subject><subject>Antidepressants</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Behavior modification</subject><subject>Behavioral medicine</subject><subject>Care and treatment</subject><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Cognitive ability</subject><subject>Cognitive behavioral therapy</subject><subject>Cognitive Therapy</subject><subject>Comorbidity</subject><subject>Depression (Mood disorder)</subject><subject>Depressive Disorder, Major - drug therapy</subject><subject>Drugs</subject><subject>Health Planning Guidelines</subject><subject>Humans</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Mental depression</subject><subject>Mental health</subject><subject>Patients</subject><subject>Polyamide-imides</subject><subject>Precision Medicine</subject><subject>Predictions</subject><subject>Prognosis</subject><subject>Psychiatric Status Rating Scales</subject><subject>Psychiatry</subject><subject>Psychology</subject><subject>Randomization</subject><subject>Regression analysis</subject><subject>Regression models</subject><subject>Researchers</subject><subject>Social and Behavioral Sciences</subject><subject>Test procedures</subject><subject>Translational Medical Research</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12L1DAUhoso7rr6D0QLguDFjPlsM14Iw-LHwMKKrt6G0yTtZGib2SQdVm_942Z2ussUFKTQHk6e9-3h5Jwse47RHNMSv924wffQzreuN3OEBBUlf5Cd4gUls4Ig-vAoPsmehLBBiFNRFI-zE8IYLnApTrPfV2uTfzE-uORlfxmdL_UO-giNyVe9Njfv8uihDy1E2ze5N8GAV-vc9fnWG21VtCm0fXTppe3O6mH0id5A7Ewfk0i5LkUa9nCY58tcmy5FyXmfeZo9qqEN5tn4Pcu-f_xwdf55dnH5aXW-vJipYkHijJia1RqqioHhCioAynHBas4RKUUlNKeEAFQckGC4wpiTUgNDBhusGNP0LHt58N22Lsixf0FiVhZYIExxIlYHQjvYyK23Hfif0oGVtwnnGwk-WtUaqREqeV2iGlTFqkJUVACFSpAFIkQvVPJ6P_5tqDqjVeqEh3ZiOj3p7Vo2biepEJyTfTGvRgPvrgcT4j9KHqkGUlW2r10yU50NSi5ZKUTJMKKJmv-FSk-6CKvSBNU25SeCNxNBYqK5iQ0MIcjVt6__z17-mLKvj9i1gTaug2uH28mYguwAKu9C8Ka-7xxGcr8Ad92Q-wWQ4wIk2Yvjrt-L7iae_gHJrARB</recordid><startdate>20140108</startdate><enddate>20140108</enddate><creator>DeRubeis, Robert J</creator><creator>Cohen, Zachary D</creator><creator>Forand, Nicholas R</creator><creator>Fournier, Jay C</creator><creator>Gelfand, Lois A</creator><creator>Lorenzo-Luaces, Lorenzo</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140108</creationdate><title>The Personalized Advantage Index: translating research on prediction into individualized treatment recommendations. 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Lorenzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Personalized Advantage Index: translating research on prediction into individualized treatment recommendations. A demonstration</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-01-08</date><risdate>2014</risdate><volume>9</volume><issue>1</issue><spage>e83875</spage><pages>e83875-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Advances in personalized medicine require the identification of variables that predict differential response to treatments as well as the development and refinement of methods to transform predictive information into actionable recommendations.
To illustrate and test a new method for integrating predictive information to aid in treatment selection, using data from a randomized treatment comparison.
Data from a trial of antidepressant medications (N = 104) versus cognitive behavioral therapy (N = 50) for Major Depressive Disorder were used to produce predictions of post-treatment scores on the Hamilton Rating Scale for Depression (HRSD) in each of the two treatments for each of the 154 patients. The patient's own data were not used in the models that yielded these predictions. Five pre-randomization variables that predicted differential response (marital status, employment status, life events, comorbid personality disorder, and prior medication trials) were included in regression models, permitting the calculation of each patient's Personalized Advantage Index (PAI), in HRSD units.
For 60% of the sample a clinically meaningful advantage (PAI≥3) was predicted for one of the treatments, relative to the other. When these patients were divided into those randomly assigned to their "Optimal" treatment versus those assigned to their "Non-optimal" treatment, outcomes in the former group were superior (d = 0.58, 95% CI .17-1.01).
This approach to treatment selection, implemented in the context of two equally effective treatments, yielded effects that, if obtained prospectively, would rival those routinely observed in comparisons of active versus control treatments.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24416178</pmid><doi>10.1371/journal.pone.0083875</doi><tpages>e83875</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Active control Analysis Antidepressants Antidepressive Agents - therapeutic use Behavior modification Behavioral medicine Care and treatment Clinical outcomes Clinical trials Cognitive ability Cognitive behavioral therapy Cognitive Therapy Comorbidity Depression (Mood disorder) Depressive Disorder, Major - drug therapy Drugs Health Planning Guidelines Humans Medical imaging Medicine Mental depression Mental health Patients Polyamide-imides Precision Medicine Predictions Prognosis Psychiatric Status Rating Scales Psychiatry Psychology Randomization Regression analysis Regression models Researchers Social and Behavioral Sciences Test procedures Translational Medical Research |
title | The Personalized Advantage Index: translating research on prediction into individualized treatment recommendations. A demonstration |
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