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547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir
BACKGROUND: The Phase 3 BRIGHTE study evaluated fostemsavir in heavily treatment experienced HIV-1 patients failing their current antiretroviral (ARV) regimen and unable to construct a viable regimen from remaining available agents. Week 24 efficacy and safety have been previously reported—fostemsav...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255559/ http://dx.doi.org/10.1093/ofid/ofy210.555 |
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author | Proudfoot, Clare Ackerman, Peter Llamoso, Cyril Cella, David Clark, Andrew Murray, Miranda |
author_facet | Proudfoot, Clare Ackerman, Peter Llamoso, Cyril Cella, David Clark, Andrew Murray, Miranda |
author_sort | Proudfoot, Clare |
collection | PubMed |
description | BACKGROUND: The Phase 3 BRIGHTE study evaluated fostemsavir in heavily treatment experienced HIV-1 patients failing their current antiretroviral (ARV) regimen and unable to construct a viable regimen from remaining available agents. Week 24 efficacy and safety have been previously reported—fostemsavir resulted in virological and immunological improvements and was generally well tolerated. The objective of this abstract is to report analyses of patient-reported outcomes (PROs) from BRIGHTE. METHODS: BRIGHTE included two cohorts: the randomized cohort (RC) had one to two classes of ARV therapy available; the nonrandomized cohort (NRC) had no ARV classes available. RC patients received fostemsavir or placebo + existing failing regimen for 8 days, and thereafter fostemsavir + optimized background therapy (OBT); NRC received fostemsavir + OBT throughout. PROs included the Functional Assessment of HIV Infection (FAHI), the EuroQol-5D-3L (EQ-5D) and associated visual analogue scale (VAS). RESULTS: Both cohorts had advanced disease, low CD4 counts (median of 99.5 in RC and 41 in NRC) and high proportions of patients with AIDS (84% in RC and 90% in NRC). This was reflected in fairly low baseline FAHI scores. Improvements from baseline to Week 24 were observed in FAHI total score, physical well-being and emotional well-being subscales, with limited/no change in function/ global well-being, social well-being and cognitive function. Improvements in the RC were close to published values for minimum clinically important differences, with smaller improvements in the NRC. EQ-5D utilities were similar at Week 24 to baseline in both cohorts, with improvements in the EQ-5D VAS (11% in the RC, 8% in the NRC). CONCLUSION: The BRIGHTE study demonstrated improvements in PROs in heavily treatment experienced HIV patients, complementing previously published efficacy and safety results. DISCLOSURES: C. Proudfoot, viiv healthcare: Employee, Salary. P. Ackerman, ViiV Healthcare: Employee, Salary. C. Llamoso, ViiV Healthcare: Employee, Salary. A. Clark, ViiV healthcare: Employee, Salary. M. Murray, Viiv healthcare: Employee, Salary. |
format | Online Article Text |
id | pubmed-6255559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62555592018-11-28 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir Proudfoot, Clare Ackerman, Peter Llamoso, Cyril Cella, David Clark, Andrew Murray, Miranda Open Forum Infect Dis Abstracts BACKGROUND: The Phase 3 BRIGHTE study evaluated fostemsavir in heavily treatment experienced HIV-1 patients failing their current antiretroviral (ARV) regimen and unable to construct a viable regimen from remaining available agents. Week 24 efficacy and safety have been previously reported—fostemsavir resulted in virological and immunological improvements and was generally well tolerated. The objective of this abstract is to report analyses of patient-reported outcomes (PROs) from BRIGHTE. METHODS: BRIGHTE included two cohorts: the randomized cohort (RC) had one to two classes of ARV therapy available; the nonrandomized cohort (NRC) had no ARV classes available. RC patients received fostemsavir or placebo + existing failing regimen for 8 days, and thereafter fostemsavir + optimized background therapy (OBT); NRC received fostemsavir + OBT throughout. PROs included the Functional Assessment of HIV Infection (FAHI), the EuroQol-5D-3L (EQ-5D) and associated visual analogue scale (VAS). RESULTS: Both cohorts had advanced disease, low CD4 counts (median of 99.5 in RC and 41 in NRC) and high proportions of patients with AIDS (84% in RC and 90% in NRC). This was reflected in fairly low baseline FAHI scores. Improvements from baseline to Week 24 were observed in FAHI total score, physical well-being and emotional well-being subscales, with limited/no change in function/ global well-being, social well-being and cognitive function. Improvements in the RC were close to published values for minimum clinically important differences, with smaller improvements in the NRC. EQ-5D utilities were similar at Week 24 to baseline in both cohorts, with improvements in the EQ-5D VAS (11% in the RC, 8% in the NRC). CONCLUSION: The BRIGHTE study demonstrated improvements in PROs in heavily treatment experienced HIV patients, complementing previously published efficacy and safety results. DISCLOSURES: C. Proudfoot, viiv healthcare: Employee, Salary. P. Ackerman, ViiV Healthcare: Employee, Salary. C. Llamoso, ViiV Healthcare: Employee, Salary. A. Clark, ViiV healthcare: Employee, Salary. M. Murray, Viiv healthcare: Employee, Salary. Oxford University Press 2018-11-26 /pmc/articles/PMC6255559/ http://dx.doi.org/10.1093/ofid/ofy210.555 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Proudfoot, Clare Ackerman, Peter Llamoso, Cyril Cella, David Clark, Andrew Murray, Miranda 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir |
title | 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir |
title_full | 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir |
title_fullStr | 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir |
title_full_unstemmed | 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir |
title_short | 547. Results of Patient-Reported Outcome Data From the Phase III BRIGHTE Study of Fostemsavir |
title_sort | 547. results of patient-reported outcome data from the phase iii brighte study of fostemsavir |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255559/ http://dx.doi.org/10.1093/ofid/ofy210.555 |
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