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Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context

BACKGROUND: Despite improvements in hemophilia care, challenges remain, including treatment burden and impaired quality of life. Gene therapy may overcome these. However, its introduction presents a challenge. OBJECTIVES: To outline a function-based gene therapy working model describing critical mil...

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Autores principales: Astermark, Jan, Baghaei, Fariba, Strandberg, Karin, Toplican, Petra Gabric, Birkedal, Maj Friberg, Grahn, Emma Engman, Hansson, Charlotta, Kampmann, Peter, Lehtinen, Anna-Elina, Täckström, Kinga, Holme, Pål Andre, Magnusson, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583513/
https://www.ncbi.nlm.nih.gov/pubmed/37859645
http://dx.doi.org/10.1177/20406207231202306
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author Astermark, Jan
Baghaei, Fariba
Strandberg, Karin
Toplican, Petra Gabric
Birkedal, Maj Friberg
Grahn, Emma Engman
Hansson, Charlotta
Kampmann, Peter
Lehtinen, Anna-Elina
Täckström, Kinga
Holme, Pål Andre
Magnusson, Maria
author_facet Astermark, Jan
Baghaei, Fariba
Strandberg, Karin
Toplican, Petra Gabric
Birkedal, Maj Friberg
Grahn, Emma Engman
Hansson, Charlotta
Kampmann, Peter
Lehtinen, Anna-Elina
Täckström, Kinga
Holme, Pål Andre
Magnusson, Maria
author_sort Astermark, Jan
collection PubMed
description BACKGROUND: Despite improvements in hemophilia care, challenges remain, including treatment burden and impaired quality of life. Gene therapy may overcome these. However, its introduction presents a challenge. OBJECTIVES: To outline a function-based gene therapy working model describing critical milestones associated with gene therapy handling, administration, and follow-up to facilitate and implement an effective infrastructure for gene therapy introduction. DESIGN: Literature review and consensus discussion among Hemophilia Comprehensive Care centers (HCCCs) in the Nordic region. METHODS: Representatives from six HCCCs sought to pinpoint milestones and key stakeholders for site readiness at the pre-, peri-, and post-infusion stages, including authority and genetically modified organism (GMO) product requirements, awareness, medical eligibility, logistics and product handling for infusion, laboratory monitoring, and follow-up. RESULTS: A gene therapy transit map was developed with key stakeholders identified. The approach to prepare the vector will differ between the Nordic centers, but the contracted pharmacy unit will be a key stakeholder. Therefore, a pharmacy checklist for the implementation of gene therapy was developed. For the future, Advanced Therapy Medicinal Product centers will also be implemented. Patients’ expectations, commitments, and concerns need to be addressed repeatedly and education of patients and the expanded health-care professionals team will be the key to successful and optimal clinical management. Eligibility testing according to the product’s summary of product characteristics and frequent follow-up and monitoring post-infusion according to the World Federation of Hemophilia chart will be crucial. CONCLUSION: The approach to deliver gene therapy in the Nordic region will differ partly between the hemophilia centers, but the defined road map with checklists for the implementation of this advanced therapy will be applicable to all. The map may also serve as a platform for the use of future GMO product options both within and outside the area of hemophilia.
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spelling pubmed-105835132023-10-19 Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context Astermark, Jan Baghaei, Fariba Strandberg, Karin Toplican, Petra Gabric Birkedal, Maj Friberg Grahn, Emma Engman Hansson, Charlotta Kampmann, Peter Lehtinen, Anna-Elina Täckström, Kinga Holme, Pål Andre Magnusson, Maria Ther Adv Hematol Original Research BACKGROUND: Despite improvements in hemophilia care, challenges remain, including treatment burden and impaired quality of life. Gene therapy may overcome these. However, its introduction presents a challenge. OBJECTIVES: To outline a function-based gene therapy working model describing critical milestones associated with gene therapy handling, administration, and follow-up to facilitate and implement an effective infrastructure for gene therapy introduction. DESIGN: Literature review and consensus discussion among Hemophilia Comprehensive Care centers (HCCCs) in the Nordic region. METHODS: Representatives from six HCCCs sought to pinpoint milestones and key stakeholders for site readiness at the pre-, peri-, and post-infusion stages, including authority and genetically modified organism (GMO) product requirements, awareness, medical eligibility, logistics and product handling for infusion, laboratory monitoring, and follow-up. RESULTS: A gene therapy transit map was developed with key stakeholders identified. The approach to prepare the vector will differ between the Nordic centers, but the contracted pharmacy unit will be a key stakeholder. Therefore, a pharmacy checklist for the implementation of gene therapy was developed. For the future, Advanced Therapy Medicinal Product centers will also be implemented. Patients’ expectations, commitments, and concerns need to be addressed repeatedly and education of patients and the expanded health-care professionals team will be the key to successful and optimal clinical management. Eligibility testing according to the product’s summary of product characteristics and frequent follow-up and monitoring post-infusion according to the World Federation of Hemophilia chart will be crucial. CONCLUSION: The approach to deliver gene therapy in the Nordic region will differ partly between the hemophilia centers, but the defined road map with checklists for the implementation of this advanced therapy will be applicable to all. The map may also serve as a platform for the use of future GMO product options both within and outside the area of hemophilia. SAGE Publications 2023-10-17 /pmc/articles/PMC10583513/ /pubmed/37859645 http://dx.doi.org/10.1177/20406207231202306 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Astermark, Jan
Baghaei, Fariba
Strandberg, Karin
Toplican, Petra Gabric
Birkedal, Maj Friberg
Grahn, Emma Engman
Hansson, Charlotta
Kampmann, Peter
Lehtinen, Anna-Elina
Täckström, Kinga
Holme, Pål Andre
Magnusson, Maria
Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
title Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
title_full Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
title_fullStr Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
title_full_unstemmed Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
title_short Infrastructural considerations of implementing gene therapy for hemophilia in the Nordic context
title_sort infrastructural considerations of implementing gene therapy for hemophilia in the nordic context
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583513/
https://www.ncbi.nlm.nih.gov/pubmed/37859645
http://dx.doi.org/10.1177/20406207231202306
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