Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation
Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs and biological products for use in pediatric setti...
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creator | Fleming, Thomas R. Garnett, Christine E. Conklin, Laurie S. Corriol-Rohou, Solange Hariharan, Sudharshan Hsu, Daphne Mueller-Velten, Guenther Mulugeta, Yeruk Portman, Ronald Rothmann, Mark D. Stockbridge, Norman L. Wandel, Simon Zhang, Jialu Yao, Lynne |
description | Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs and biological products for use in pediatric settings, as in adults, requires demonstration of substantial evidence of effectiveness and favorable benefit-to-risk. For diseases primarily affecting children, such evidence predominantly would be obtained in the pediatric setting. However, for conditions affecting both adults and children, pediatric extrapolation uses scientific evidence in adults to enable more efficiently obtaining a reliable evaluation of an intervention’s effects in pediatric populations. Bridging biomarkers potentially have an integral role in pediatric extrapolation. In a setting where an intervention reliably has been established to be safe and effective in adults, and where there is substantive evidence that disease processes in pediatric and adult settings are biologically similar, a ‘bridging biomarker’ should satisfy three additional criteria: effects on the bridging biomarker should capture effects on the principal causal pathway through which the disease process meaningfully influences ‘feels, functions, survives’ measures; secondly, the experimental intervention should not have important unintended effects on ‘feels, functions, survives’ measures not captured by the bridging biomarker; and thirdly, in statistical analyses in adults, the intervention’s net effect on ‘feels, functions, survives’ measures should be consistent with what would be predicted by its level of effect on the bridging biomarker. A validated bridging biomarker has considerable potential utility, since an intervention’s efficacy could be extrapolated from adult to pediatric populations if evidence in children establishes the intervention not only to be safe but also to have substantive effects on that bridging biomarker. Proper use of bridging biomarkers could increase availability of reliably evaluated therapies approved for use in pediatric settings, enabling children and their caregivers to make informed choices about health care. |
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The approval of prescription drugs and biological products for use in pediatric settings, as in adults, requires demonstration of substantial evidence of effectiveness and favorable benefit-to-risk. For diseases primarily affecting children, such evidence predominantly would be obtained in the pediatric setting. However, for conditions affecting both adults and children, pediatric extrapolation uses scientific evidence in adults to enable more efficiently obtaining a reliable evaluation of an intervention’s effects in pediatric populations. Bridging biomarkers potentially have an integral role in pediatric extrapolation. In a setting where an intervention reliably has been established to be safe and effective in adults, and where there is substantive evidence that disease processes in pediatric and adult settings are biologically similar, a ‘bridging biomarker’ should satisfy three additional criteria: effects on the bridging biomarker should capture effects on the principal causal pathway through which the disease process meaningfully influences ‘feels, functions, survives’ measures; secondly, the experimental intervention should not have important unintended effects on ‘feels, functions, survives’ measures not captured by the bridging biomarker; and thirdly, in statistical analyses in adults, the intervention’s net effect on ‘feels, functions, survives’ measures should be consistent with what would be predicted by its level of effect on the bridging biomarker. A validated bridging biomarker has considerable potential utility, since an intervention’s efficacy could be extrapolated from adult to pediatric populations if evidence in children establishes the intervention not only to be safe but also to have substantive effects on that bridging biomarker. Proper use of bridging biomarkers could increase availability of reliably evaluated therapies approved for use in pediatric settings, enabling children and their caregivers to make informed choices about health care.</description><identifier>ISSN: 2168-4790</identifier><identifier>EISSN: 2168-4804</identifier><identifier>DOI: 10.1007/s43441-022-00445-6</identifier><identifier>PMID: 36057747</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adult ; Adults ; Biomarkers ; Caregivers ; Child ; Children ; Drug development ; Drug Safety and Pharmacovigilance ; Evaluation ; Extrapolation ; Health care ; Health risks ; Humans ; Intervention ; Medical innovations ; Medical treatment ; Medicine ; Original Research ; Pediatrics ; Pharmacotherapy ; Pharmacy ; Populations ; Risk Assessment ; Statistical analysis ; Survival</subject><ispartof>Therapeutic innovation & regulatory science, 2023-01, Vol.57 (1), p.109-120</ispartof><rights>This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022</rights><rights>2022. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.</rights><rights>This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-aee99f5598aa8e0f2b0a28cb1d49c822c794a6df1c72e68b0c74ba323cc88ae03</citedby><cites>FETCH-LOGICAL-c474t-aee99f5598aa8e0f2b0a28cb1d49c822c794a6df1c72e68b0c74ba323cc88ae03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s43441-022-00445-6$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s43441-022-00445-6$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,777,781,882,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36057747$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fleming, Thomas R.</creatorcontrib><creatorcontrib>Garnett, Christine E.</creatorcontrib><creatorcontrib>Conklin, Laurie S.</creatorcontrib><creatorcontrib>Corriol-Rohou, Solange</creatorcontrib><creatorcontrib>Hariharan, Sudharshan</creatorcontrib><creatorcontrib>Hsu, Daphne</creatorcontrib><creatorcontrib>Mueller-Velten, Guenther</creatorcontrib><creatorcontrib>Mulugeta, Yeruk</creatorcontrib><creatorcontrib>Portman, Ronald</creatorcontrib><creatorcontrib>Rothmann, Mark D.</creatorcontrib><creatorcontrib>Stockbridge, Norman L.</creatorcontrib><creatorcontrib>Wandel, Simon</creatorcontrib><creatorcontrib>Zhang, Jialu</creatorcontrib><creatorcontrib>Yao, Lynne</creatorcontrib><title>Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation</title><title>Therapeutic innovation & regulatory science</title><addtitle>Ther Innov Regul Sci</addtitle><addtitle>Ther Innov Regul Sci</addtitle><description>Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs and biological products for use in pediatric settings, as in adults, requires demonstration of substantial evidence of effectiveness and favorable benefit-to-risk. For diseases primarily affecting children, such evidence predominantly would be obtained in the pediatric setting. However, for conditions affecting both adults and children, pediatric extrapolation uses scientific evidence in adults to enable more efficiently obtaining a reliable evaluation of an intervention’s effects in pediatric populations. Bridging biomarkers potentially have an integral role in pediatric extrapolation. In a setting where an intervention reliably has been established to be safe and effective in adults, and where there is substantive evidence that disease processes in pediatric and adult settings are biologically similar, a ‘bridging biomarker’ should satisfy three additional criteria: effects on the bridging biomarker should capture effects on the principal causal pathway through which the disease process meaningfully influences ‘feels, functions, survives’ measures; secondly, the experimental intervention should not have important unintended effects on ‘feels, functions, survives’ measures not captured by the bridging biomarker; and thirdly, in statistical analyses in adults, the intervention’s net effect on ‘feels, functions, survives’ measures should be consistent with what would be predicted by its level of effect on the bridging biomarker. A validated bridging biomarker has considerable potential utility, since an intervention’s efficacy could be extrapolated from adult to pediatric populations if evidence in children establishes the intervention not only to be safe but also to have substantive effects on that bridging biomarker. Proper use of bridging biomarkers could increase availability of reliably evaluated therapies approved for use in pediatric settings, enabling children and their caregivers to make informed choices about health care.</description><subject>Adult</subject><subject>Adults</subject><subject>Biomarkers</subject><subject>Caregivers</subject><subject>Child</subject><subject>Children</subject><subject>Drug development</subject><subject>Drug Safety and Pharmacovigilance</subject><subject>Evaluation</subject><subject>Extrapolation</subject><subject>Health care</subject><subject>Health risks</subject><subject>Humans</subject><subject>Intervention</subject><subject>Medical innovations</subject><subject>Medical treatment</subject><subject>Medicine</subject><subject>Original Research</subject><subject>Pediatrics</subject><subject>Pharmacotherapy</subject><subject>Pharmacy</subject><subject>Populations</subject><subject>Risk Assessment</subject><subject>Statistical analysis</subject><subject>Survival</subject><issn>2168-4790</issn><issn>2168-4804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU9P3DAQxa2qVUGUL8ABWeqll7QTx4ltDpXKn7ZISHCAs-U4k11D1k7tZAXql69hgVIO9WUszW_ezNMjZK-EzyWA-JJ4xXlZAGMFAOd10bwh26xsZMEl8LdPf6Fgi-ymdA35KVkLJt-TraqBWggutsnvU-_D2kwu-ESdpxfYOTNFZ-nlEqMZcZ6cTfQY1ziEcYV-OqAX0XnrxgET7UOk0xLpVUIaenoYXbdwfkEPXViZeIPxlejJ7ZRFw_Cw8AN515sh4e5j3SFX308uj34WZ-c_To--nRWWCz4VBlGpvq6VNEYi9KwFw6Rty44rKxmzQnHTdH1pBcNGtmAFb03FKmulNAjVDvm60R3ndoWdzSaiGfQYXb7xTgfj9L8d75Z6EdZaiboGybPAp0eBGH7NmCa9csniMBiPYU6aCVCCVwLKjH58hV6HOfpsL1M1lzKTTabYhrIxpBSxfz6mBH0fr97Eq3O8-iFefT-0_9LG88hTmBmoNkDKLb_A-Hf3f2T_AJTRs0g</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Fleming, Thomas R.</creator><creator>Garnett, Christine E.</creator><creator>Conklin, Laurie S.</creator><creator>Corriol-Rohou, Solange</creator><creator>Hariharan, Sudharshan</creator><creator>Hsu, Daphne</creator><creator>Mueller-Velten, Guenther</creator><creator>Mulugeta, Yeruk</creator><creator>Portman, Ronald</creator><creator>Rothmann, Mark D.</creator><creator>Stockbridge, Norman L.</creator><creator>Wandel, Simon</creator><creator>Zhang, Jialu</creator><creator>Yao, Lynne</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</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><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230101</creationdate><title>Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation</title><author>Fleming, Thomas R. ; Garnett, Christine E. ; Conklin, Laurie S. ; Corriol-Rohou, Solange ; Hariharan, Sudharshan ; Hsu, Daphne ; Mueller-Velten, Guenther ; Mulugeta, Yeruk ; Portman, Ronald ; Rothmann, Mark D. ; Stockbridge, Norman L. ; Wandel, Simon ; Zhang, Jialu ; Yao, Lynne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-aee99f5598aa8e0f2b0a28cb1d49c822c794a6df1c72e68b0c74ba323cc88ae03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Adults</topic><topic>Biomarkers</topic><topic>Caregivers</topic><topic>Child</topic><topic>Children</topic><topic>Drug development</topic><topic>Drug Safety and Pharmacovigilance</topic><topic>Evaluation</topic><topic>Extrapolation</topic><topic>Health care</topic><topic>Health risks</topic><topic>Humans</topic><topic>Intervention</topic><topic>Medical innovations</topic><topic>Medical treatment</topic><topic>Medicine</topic><topic>Original Research</topic><topic>Pediatrics</topic><topic>Pharmacotherapy</topic><topic>Pharmacy</topic><topic>Populations</topic><topic>Risk Assessment</topic><topic>Statistical analysis</topic><topic>Survival</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fleming, Thomas R.</creatorcontrib><creatorcontrib>Garnett, Christine E.</creatorcontrib><creatorcontrib>Conklin, Laurie S.</creatorcontrib><creatorcontrib>Corriol-Rohou, Solange</creatorcontrib><creatorcontrib>Hariharan, Sudharshan</creatorcontrib><creatorcontrib>Hsu, Daphne</creatorcontrib><creatorcontrib>Mueller-Velten, Guenther</creatorcontrib><creatorcontrib>Mulugeta, Yeruk</creatorcontrib><creatorcontrib>Portman, Ronald</creatorcontrib><creatorcontrib>Rothmann, Mark D.</creatorcontrib><creatorcontrib>Stockbridge, Norman L.</creatorcontrib><creatorcontrib>Wandel, Simon</creatorcontrib><creatorcontrib>Zhang, Jialu</creatorcontrib><creatorcontrib>Yao, Lynne</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Therapeutic innovation & regulatory science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fleming, Thomas R.</au><au>Garnett, Christine E.</au><au>Conklin, Laurie S.</au><au>Corriol-Rohou, Solange</au><au>Hariharan, Sudharshan</au><au>Hsu, Daphne</au><au>Mueller-Velten, Guenther</au><au>Mulugeta, Yeruk</au><au>Portman, Ronald</au><au>Rothmann, Mark D.</au><au>Stockbridge, Norman L.</au><au>Wandel, Simon</au><au>Zhang, Jialu</au><au>Yao, Lynne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation</atitle><jtitle>Therapeutic innovation & regulatory science</jtitle><stitle>Ther Innov Regul Sci</stitle><addtitle>Ther Innov Regul Sci</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>57</volume><issue>1</issue><spage>109</spage><epage>120</epage><pages>109-120</pages><issn>2168-4790</issn><eissn>2168-4804</eissn><abstract>Even with recent substantive improvements in health care in pediatric populations, considerable need remains for additional safe and effective interventions for the prevention and treatment of diseases in children. The approval of prescription drugs and biological products for use in pediatric settings, as in adults, requires demonstration of substantial evidence of effectiveness and favorable benefit-to-risk. For diseases primarily affecting children, such evidence predominantly would be obtained in the pediatric setting. However, for conditions affecting both adults and children, pediatric extrapolation uses scientific evidence in adults to enable more efficiently obtaining a reliable evaluation of an intervention’s effects in pediatric populations. Bridging biomarkers potentially have an integral role in pediatric extrapolation. In a setting where an intervention reliably has been established to be safe and effective in adults, and where there is substantive evidence that disease processes in pediatric and adult settings are biologically similar, a ‘bridging biomarker’ should satisfy three additional criteria: effects on the bridging biomarker should capture effects on the principal causal pathway through which the disease process meaningfully influences ‘feels, functions, survives’ measures; secondly, the experimental intervention should not have important unintended effects on ‘feels, functions, survives’ measures not captured by the bridging biomarker; and thirdly, in statistical analyses in adults, the intervention’s net effect on ‘feels, functions, survives’ measures should be consistent with what would be predicted by its level of effect on the bridging biomarker. A validated bridging biomarker has considerable potential utility, since an intervention’s efficacy could be extrapolated from adult to pediatric populations if evidence in children establishes the intervention not only to be safe but also to have substantive effects on that bridging biomarker. Proper use of bridging biomarkers could increase availability of reliably evaluated therapies approved for use in pediatric settings, enabling children and their caregivers to make informed choices about health care.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>36057747</pmid><doi>10.1007/s43441-022-00445-6</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adults Biomarkers Caregivers Child Children Drug development Drug Safety and Pharmacovigilance Evaluation Extrapolation Health care Health risks Humans Intervention Medical innovations Medical treatment Medicine Original Research Pediatrics Pharmacotherapy Pharmacy Populations Risk Assessment Statistical analysis Survival |
title | Innovations in Pediatric Therapeutics Development: Principles for the Use of Bridging Biomarkers in Pediatric Extrapolation |
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