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The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients
BACKGROUND: The phase ½ hemophilia B clinical trial (AMT-060) demonstrated stable endogenous FIX levels after 3.5 years (mean FIX activity between 5.1% and 7.5%) with continued reductions in annualized bleeds to near zero with the higher dose, and a 78–96% reduction by year in exogenous FIX use. OBJ...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184858/ https://www.ncbi.nlm.nih.gov/pubmed/32368018 http://dx.doi.org/10.2147/PPA.S239810 |
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author | Miesbach, Wolfgang Klamroth, Robert |
author_facet | Miesbach, Wolfgang Klamroth, Robert |
author_sort | Miesbach, Wolfgang |
collection | PubMed |
description | BACKGROUND: The phase ½ hemophilia B clinical trial (AMT-060) demonstrated stable endogenous FIX levels after 3.5 years (mean FIX activity between 5.1% and 7.5%) with continued reductions in annualized bleeds to near zero with the higher dose, and a 78–96% reduction by year in exogenous FIX use. OBJECTIVE: The views of all the three participants from Germany participating in the AMT-060 study have been investigated about their experiences with conventional and gene therapy and the effects of the forms of therapy on everyday life. PATIENTS/METHODS: The patients (aged 33–35 years) performed regular prophylactic replacement with factor IX concentrate prior to the gene therapy, reported 0–7 bleeds in the year prior to the treatment, with Hemophilia Joint Health Scores of 0–8. Following topics have been investigated “dealing with illness”, “participation in studies”, “perception of conventional therapy”, “perception of gene therapy”, “significance of participation in gene therapy studies”, “therapy of haemophilia after the end of the study”. RESULTS: All three participants have started to become more active and do more sports. However, they expressed anxiety about not knowing how long the effect would last and they felt that psychological support would be needed if the factor IX level fell back in the future. No patient expressed concern about any long-term potential negative consequences of gene therapy. CONCLUSION: Gene therapy has the potential to change the life of patients with haemophilia not only by the reduction of bleeding events but also by the increase of active and sportive activities. |
format | Online Article Text |
id | pubmed-7184858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-71848582020-05-04 The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients Miesbach, Wolfgang Klamroth, Robert Patient Prefer Adherence Case Series BACKGROUND: The phase ½ hemophilia B clinical trial (AMT-060) demonstrated stable endogenous FIX levels after 3.5 years (mean FIX activity between 5.1% and 7.5%) with continued reductions in annualized bleeds to near zero with the higher dose, and a 78–96% reduction by year in exogenous FIX use. OBJECTIVE: The views of all the three participants from Germany participating in the AMT-060 study have been investigated about their experiences with conventional and gene therapy and the effects of the forms of therapy on everyday life. PATIENTS/METHODS: The patients (aged 33–35 years) performed regular prophylactic replacement with factor IX concentrate prior to the gene therapy, reported 0–7 bleeds in the year prior to the treatment, with Hemophilia Joint Health Scores of 0–8. Following topics have been investigated “dealing with illness”, “participation in studies”, “perception of conventional therapy”, “perception of gene therapy”, “significance of participation in gene therapy studies”, “therapy of haemophilia after the end of the study”. RESULTS: All three participants have started to become more active and do more sports. However, they expressed anxiety about not knowing how long the effect would last and they felt that psychological support would be needed if the factor IX level fell back in the future. No patient expressed concern about any long-term potential negative consequences of gene therapy. CONCLUSION: Gene therapy has the potential to change the life of patients with haemophilia not only by the reduction of bleeding events but also by the increase of active and sportive activities. Dove 2020-04-22 /pmc/articles/PMC7184858/ /pubmed/32368018 http://dx.doi.org/10.2147/PPA.S239810 Text en © 2020 Miesbach and Klamroth. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Case Series Miesbach, Wolfgang Klamroth, Robert The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients |
title | The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients |
title_full | The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients |
title_fullStr | The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients |
title_full_unstemmed | The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients |
title_short | The Patient Experience of Gene Therapy for Hemophilia: Qualitative Interviews with Trial Patients |
title_sort | patient experience of gene therapy for hemophilia: qualitative interviews with trial patients |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7184858/ https://www.ncbi.nlm.nih.gov/pubmed/32368018 http://dx.doi.org/10.2147/PPA.S239810 |
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