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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...

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Autores principales: Proudfoot, Clare, Ackerman, Peter, Llamoso, Cyril, Cella, David, Clark, Andrew, Murray, Miranda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
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.
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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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