Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi

Detalhes bibliográficos
Autor(a) principal: Wiesinger, Anna-Maria
Data de Publicação: 2023
Outros Autores: Bigger, Brian, Giugliani, Roberto, Lampe, Christina, Scarpa, Maurizio, Moser, Tobias, Kampmann, Christoph, Zimmermann, Georg, Lagler, Florian B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/276423
Resumo: Mucopolysaccharidosis (MPS) is a group of rare metabolic diseases associated with reduced life expectancy and a substantial unmet medical need. Immunomodulatory drugs could be a relevant treatment approach for MPS patients, although they are not licensed for this population. Therefore, we aim to provide evidence justifying fast access to innovative individual treatment trials (ITTs) with immunomodulators and a high-quality evaluation of drug effects by implementing a risk-benefit model for MPS. The iterative methodology of our developed decision analysis framework (DAF) consists of the following steps: (i) a comprehensive literature analysis on promising treatment targets and immunomodulators for MPS; (ii) a quantitative risk-benefit assessment (RBA) of selected molecules; and (iii) allocation phenotypic profiles and a quantitative assessment. These steps allow for the personalized use of the model and are in accordance with expert and patient representatives. The following four promising immunomodulators were identified: adalimumab, abatacept, anakinra, and cladribine. An improvement in mobility is most likely with adalimumab, while anakinra might be the treatment of choice for patients with neurocognitive involvement. Nevertheless, a RBA should always be completed on an individual basis. Our evidence-based DAF model for ITTs directly addresses the substantial unmet medical need in MPS and characterizes a first approach toward precision medicine with immunomodulatory drugs.
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spelling Wiesinger, Anna-MariaBigger, BrianGiugliani, RobertoLampe, ChristinaScarpa, MaurizioMoser, TobiasKampmann, ChristophZimmermann, GeorgLagler, Florian B.2024-07-17T05:37:56Z20231999-4923http://hdl.handle.net/10183/276423001198069Mucopolysaccharidosis (MPS) is a group of rare metabolic diseases associated with reduced life expectancy and a substantial unmet medical need. Immunomodulatory drugs could be a relevant treatment approach for MPS patients, although they are not licensed for this population. Therefore, we aim to provide evidence justifying fast access to innovative individual treatment trials (ITTs) with immunomodulators and a high-quality evaluation of drug effects by implementing a risk-benefit model for MPS. The iterative methodology of our developed decision analysis framework (DAF) consists of the following steps: (i) a comprehensive literature analysis on promising treatment targets and immunomodulators for MPS; (ii) a quantitative risk-benefit assessment (RBA) of selected molecules; and (iii) allocation phenotypic profiles and a quantitative assessment. These steps allow for the personalized use of the model and are in accordance with expert and patient representatives. The following four promising immunomodulators were identified: adalimumab, abatacept, anakinra, and cladribine. An improvement in mobility is most likely with adalimumab, while anakinra might be the treatment of choice for patients with neurocognitive involvement. Nevertheless, a RBA should always be completed on an individual basis. Our evidence-based DAF model for ITTs directly addresses the substantial unmet medical need in MPS and characterizes a first approach toward precision medicine with immunomodulatory drugs.application/pdfengPharmaceutics. Basel. Vol. 15, n. 5 (2023), 1565, 15 p.MucopolissacaridosesMedicina de precisãoImunomodulacaoMedição de riscoMucopolysaccharidosisPersonalized medicineIndividual treatment trialsImmunomodulationRisk–benefit assessmentDecision analysis frameworkRetracted: an innovative tool for evidence-based, personalized treatment trials in MucopolysaccharidosiAn innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi Estrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001198069.pdf.txt001198069.pdf.txtExtracted Texttext/plain66952http://www.lume.ufrgs.br/bitstream/10183/276423/3/001198069.pdf.txtb32a27ead92b2a70f81ce1e8b59a1963MD53001198069-02.pdf.txt001198069-02.pdf.txtExtracted Texttext/plain4544http://www.lume.ufrgs.br/bitstream/10183/276423/4/001198069-02.pdf.txt65480138bb5ca91e89de68853ba75505MD54ORIGINAL001198069.pdfTexto completo (inglês)application/pdf2092853http://www.lume.ufrgs.br/bitstream/10183/276423/1/001198069.pdfd8357fc6af546e14e74baaf781656c5eMD51001198069-02.pdfRetrataçãoapplication/pdf181712http://www.lume.ufrgs.br/bitstream/10183/276423/2/001198069-02.pdf954bbeb2c965e722d5ad736c4229a212MD5210183/2764232024-07-18 06:15:53.915287oai:www.lume.ufrgs.br:10183/276423Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-07-18T09:15:53Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
dc.title.alternative.en.fl_str_mv An innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
title Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
spellingShingle Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
Wiesinger, Anna-Maria
Mucopolissacaridoses
Medicina de precisão
Imunomodulacao
Medição de risco
Mucopolysaccharidosis
Personalized medicine
Individual treatment trials
Immunomodulation
Risk–benefit assessment
Decision analysis framework
title_short Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
title_full Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
title_fullStr Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
title_full_unstemmed Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
title_sort Retracted: an innovative tool for evidence-based, personalized treatment trials in Mucopolysaccharidosi
author Wiesinger, Anna-Maria
author_facet Wiesinger, Anna-Maria
Bigger, Brian
Giugliani, Roberto
Lampe, Christina
Scarpa, Maurizio
Moser, Tobias
Kampmann, Christoph
Zimmermann, Georg
Lagler, Florian B.
author_role author
author2 Bigger, Brian
Giugliani, Roberto
Lampe, Christina
Scarpa, Maurizio
Moser, Tobias
Kampmann, Christoph
Zimmermann, Georg
Lagler, Florian B.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Wiesinger, Anna-Maria
Bigger, Brian
Giugliani, Roberto
Lampe, Christina
Scarpa, Maurizio
Moser, Tobias
Kampmann, Christoph
Zimmermann, Georg
Lagler, Florian B.
dc.subject.por.fl_str_mv Mucopolissacaridoses
Medicina de precisão
Imunomodulacao
Medição de risco
topic Mucopolissacaridoses
Medicina de precisão
Imunomodulacao
Medição de risco
Mucopolysaccharidosis
Personalized medicine
Individual treatment trials
Immunomodulation
Risk–benefit assessment
Decision analysis framework
dc.subject.eng.fl_str_mv Mucopolysaccharidosis
Personalized medicine
Individual treatment trials
Immunomodulation
Risk–benefit assessment
Decision analysis framework
description Mucopolysaccharidosis (MPS) is a group of rare metabolic diseases associated with reduced life expectancy and a substantial unmet medical need. Immunomodulatory drugs could be a relevant treatment approach for MPS patients, although they are not licensed for this population. Therefore, we aim to provide evidence justifying fast access to innovative individual treatment trials (ITTs) with immunomodulators and a high-quality evaluation of drug effects by implementing a risk-benefit model for MPS. The iterative methodology of our developed decision analysis framework (DAF) consists of the following steps: (i) a comprehensive literature analysis on promising treatment targets and immunomodulators for MPS; (ii) a quantitative risk-benefit assessment (RBA) of selected molecules; and (iii) allocation phenotypic profiles and a quantitative assessment. These steps allow for the personalized use of the model and are in accordance with expert and patient representatives. The following four promising immunomodulators were identified: adalimumab, abatacept, anakinra, and cladribine. An improvement in mobility is most likely with adalimumab, while anakinra might be the treatment of choice for patients with neurocognitive involvement. Nevertheless, a RBA should always be completed on an individual basis. Our evidence-based DAF model for ITTs directly addresses the substantial unmet medical need in MPS and characterizes a first approach toward precision medicine with immunomodulatory drugs.
publishDate 2023
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dc.date.accessioned.fl_str_mv 2024-07-17T05:37:56Z
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dc.identifier.issn.pt_BR.fl_str_mv 1999-4923
dc.identifier.nrb.pt_BR.fl_str_mv 001198069
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Pharmaceutics. Basel. Vol. 15, n. 5 (2023), 1565, 15 p.
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