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Enregistrement W3215668940 · doi:10.1182/blood-2021-146021

Health-Related Quality of Life Following Valoctocogene Roxaparvovec Gene Therapy for Severe Hemophilia A in the Phase 3 Trial GENEr8-1

2021· article· en· W3215668940 sur OpenAlexaff
Brian O’Mahony, Johnny Mahlangu, Kathelijne Peerlinck, Jiaan‐Der Wang, Gillian Lowe, Chee-Wee Tan, Adam Giermasz, Huyen Tran, Teh‐Liane Khoo, Erin Cockrell, Dominic Pepperell, Hérvè Chambost, María Fernanda López Fernández, Rashid Kazmi, Elaine M. Majerus, Mark W. Skinner, Robert Klamroth, Jennifer Quinn, Hua Yu, Wing Yen Wong, Adebayo Lawal, Tara M. Robinson, Benjamin Kim

Notice bibliographique

RevueBlood · 2021
Typearticle
Langueen
DomaineMedicine
ThématiqueHemophilia Treatment and Research
Établissements canadiensMcMaster University
Organismes subventionnairesnon disponible
Mots-clésMedicineHaemophiliaQuality of life (healthcare)WorryHaemophilia AInternal medicinePhysical therapyPediatricsAnxietyPsychiatry

Résumé

récupéré en direct d'OpenAlex

Abstract Introduction. Severe hemophilia A (HA) negatively impacts health-related quality of life (HRQOL) through joint pain and disability, treatment burden, and effects on mental and emotional health; chronic pain and mental health are core outcomes for hemophilia gene therapy trials (Iorio, et al. Haemophilia 2018;24[4]:e167-72). In the phase 3 trial GENEr8-1 (NCT03370913), men with severe HA who received valoctocogene roxaparvovec (AAV5-hFVIII-SQ) gene therapy experienced a significant increase in endogenous FVIII activity that resulted in reduced bleeding events and FVIII utilization from baseline through 52 weeks (Ozelo, et al. Res Pract Thromb Haemost 2021;5). Here, we analyzed the impact of valoctocogene roxaparvovec on HRQOL. Methods. Men ≥18 years of age with FVIII ≤1 IU/dL previously receiving standard-of-care FVIII prophylaxis and without history of FVIII inhibitors received one 6x10 13 vg/kg valoctocogene roxaparvovec infusion. This analysis included HIV-negative participants who completed the weeks 49-52 visit. Participants completed QOL questionnaires at baseline and weeks 4, 12, 26, and 52 post-gene therapy infusion. Change from baseline was assessed with a two-sided t-test without multiplicity control. Missing data were not imputed. Measures included the hemophilia-specific Haemo-QOL-A questionnaire, which consists of 6 domain scores (Physical Functioning, Role Functioning, Consequences of Bleeding, Worry, Emotional Impact, Treatment Concern) and Total Score ranging from 0-100 (Rentz, et al. Haemophilia 2008;14[5]:1023-34); and the EQ-5D-5L, a general measure of HRQOL that assesses functional dimensions (Mobility, Self-Care, Usual Activities) as well as Pain/Discomfort and Anxiety/Depression (Herdman, et al. Qual Life Res 2011;20[10]:1727-36). EQ-5D-5L results are reported as visual analog scale (VAS; range, 0-100) and Utility Index Score (range, 0-1), which is calculated from population norms (Janssen, et al. Qual Life Res 2013;22[7]:171-27). Higher scores indicate better HRQOL. The anchor-based clinically important differences (CID) used for the Haemo-QOL-A were 5.5 for Total Score and 6 for domain scores (Quinn, et al. Abstract, Hemophilia Federation of America Virtual Conference, Aug 2020). For the EQ-5D-5L Index, 0.03 was considered a CID (Kaplan. COPD 2005;2[1]:91-7). However, use of general population norms, together with the presence of a disability paradox in hemophilia, causes the EQ-5D-5L to underestimate the negative impact of hemophilia on HRQOL (O'Hara, et al. Haemophilia 2021;27[2]:245-52), likely leading to underestimation of changes in HRQOL. Results. This analysis included 132 participants. At baseline, mean ± standard deviation (SD) Haemo-QOL-A Total Score was 75.7 ± 16.7 (n = 130); at weeks 26 and 52, mean change from baseline in Total Score demonstrated improvement (P <0.0001) at or above the CID threshold (Table). Improvement in Total Score was noted as early as 4 weeks (change from baseline, 3.0 ± 8.5; P = 0.0001) and by week 12 had reached the CID (5.5 ± 8.4; P <0.0001). Domain scores for Physical Function, Role Functioning, and Consequences of Bleeding also improved from baseline (P <0.0001), exceeding the CID at weeks 26 and 52 (Table). Treatment Concern demonstrated improvement from baseline (P <0.001) at weeks 26 and 52, exceeding the CID at week 52. Improvements below the CID were noted for Worry at weeks 26 and 52 (P <0.01) and Emotional Impact at week 52 (P <0.05; Table). At baseline, EQ-5D-5L VAS mean ± SD was 80.1 ± 15.3 (n = 131), which increased by 2.5 ± 13.7 (n = 129) at week 26 and 4.5 ± 13.3 (n = 129) at week 52. Mean ± SD EQ-5D-5L Index Score at baseline was 0.78 ± 0.17 (n = 131); mean ± SD changes from baseline at both week 26 (0.04 ± 0.14 [n = 128]) and 52 (0.04 ± 0.16 [n = 129]) demonstrated improvement (P ≤0.002), exceeding the CID of 0.03. Conclusions. These data demonstrate improvement in core outcomes of mental health (EQ-5D-5L Anxiety/Depression, Haemo-QOL-A Consequences of Bleeding) and pain and discomfort (EQ-5D-5L Pain/Discomfort, Haemo-QOL-A Physical Functioning) as well as ability to perform activities of daily living (EQ-5D-5L Self-Care and Mobility, Haemo-QOL-A Physical Functioning and Role Functioning) for participants with HA following treatment with valoctocogene roxaparvovec compared with their values on standard-of-care FVIII prophylaxis. Figure 1 Figure 1. Disclosures O'Mahony: Freeline: Consultancy; Uniqure: Speakers Bureau; BioMarin Pharmaceutical Inc.: Consultancy. Mahlangu: Baxalta: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Catalyst Biosciences: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; CSL Behring: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Novo Nordisk: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Roche: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding, Speakers Bureau; Biomarin: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Univeristy of the Witwatersrand: Current Employment; Spark: Consultancy, Membership on an entity's Board of Directors or advisory committees, Research Funding; Novartis: Research Funding; Pfizer: Research Funding; Unique: Research Funding; Sanofi: Research Funding, Speakers Bureau; Takeda: Speakers Bureau; WFH: Speakers Bureau; ISTH: Speakers Bureau; Springer: Speakers Bureau. Peerlinck: SOBI: Consultancy, Research Funding; Octapharma: Consultancy; NovoNordisk: Consultancy, Research Funding; Pfizer: Consultancy; Roche: Other: Clinical trial investigator, Research Funding; CSL Behring: Research Funding; Uniqure: Other: Clinical trial investigator; BIoMarin: Other: Clinical trial investigator. Lowe: Biomarin: Research Funding; Novartis: Honoraria; Sobi: Honoraria; Leo: Honoraria; Alexion: Honoraria; Takeda: Honoraria; NovoNordisk: Honoraria. Giermasz: Bayer: Consultancy; ATHN: Consultancy; NovoNordisk: Consultancy; UniQure: Consultancy, Research Funding; Sanofi Genzyme: Consultancy; Bioverativ/Sanofi: Consultancy, Research Funding, Speakers Bureau; Sangamo Therapeutics,: Research Funding; Pfizer: Consultancy; Genentech/Roche: Consultancy, Research Funding, Speakers Bureau; BioMarin: Consultancy, Research Funding. Cockrell: Takeda: Consultancy; CSL Behring: Consultancy; HEMA Biologics: Consultancy; Sanofi: Consultancy; BioMarin: Consultancy; Novo Nordisk: Consultancy; Genentech: Consultancy, Speakers Bureau. Pepperell: Pfizer: Other: Travel support. Chambost: Bayer: Consultancy; BioMarin: Consultancy, Other: Clinical trial investigator; travel support, Speakers Bureau; Roche: Consultancy, Other: Clinical trial investigator; travel support, Speakers Bureau; Sobi: Consultancy, Other: Clinical trial investigator; travel support, Speakers Bureau; Bioverativ: Other: Clinical trial investigator; CSL Behring: Other: Clinical trial investigator; travel support; LFB: Other: Clinical trial investigator; Octapharma: Other: Clinical trial investigator; travel support; Pfizer: Other: clinical trial investigator, Speakers Bureau. Majerus: BioMarin Pharmaceutical Inc.: Consultancy, Other: Clinical trial investigator, Travel support. Skinner: Bayer: Consultancy; BioMarin: Consultancy, Research Funding; Pfizer (DMC): Consultancy; Roche/Genentech: Consultancy, Research Funding; Sanofi: Consultancy; Spark (DMC): Consultancy; Takeda: Consultancy, Research Funding; Freeline: Research Funding; uniQure: Research Funding. Klamroth: Bayer: Consultancy, Other: Clinical trial investigator, Travel support, Research Funding, Speakers Bureau; CSL Behring: Consultancy, Other: Clinical trial investigator, Travel support, Research Funding, Speakers Bureau; Novo Nordisk: Consultancy, Other: Clinical trial investigator, Travel support, Research Funding, Speakers Bureau; Pfizer: Consultancy, Other: Clinical trial investigator, Travel support, Research Funding, Speakers Bureau; Shire (a Takeda company): Consultancy, Other: Clinical trial investigator, Travel support, Research Funding, Speakers Bureau; BioMarin: Consultancy, Other: Clinical trial investigator, Travel support, Speakers Bureau; Biotest: Consultancy, Other: Travel support, Speakers Bureau; Roche/Cugai: Consultancy, Other: Clinical trial investigator, Travel support, Speakers Bureau; Octapharma: Consultancy, Other: Clinical trial investigator, Travel support, Speakers Bureau; Sanofi: Consultancy, Other: Clinical trial investigator, Travel support, Speakers Bureau; Sobi: Consultancy, Other, Speakers Bureau; Uniqure: Consultancy, Other; LEO: Other, Research Funding, Speakers Bureau; Daiichi Sankyo: Other, Speakers Bureau; Grifols: Speakers Bureau. Quinn: BioMarin Pharmaceutical: Current Employment, Current equity holder in publicly-traded company. Yu: BioMarin Pharmaceutical: Current Employment, Current equity holder in publicly-traded company. Wong: BioMarin Pharmaceutical Inc.: Current Employment, Current equity holder in publicly-traded company. Lawal: BioMarin Pharmaceutical Inc.: Current equity holder in publicly-traded company, Ended employment in the past 24 months. Robinson: BioMarin Pharmaceutical Inc.: Current Employment, Current equity holder in publicly-traded company. Kim: BioMarin Pharmaceutical Inc.: Current Employment, Current equity holder in publicly-traded company.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,002
score de la tête « metaresearch » (Gemma)0,001
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Essai randomisé · Signal consensuel: Essai randomisé
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,002
Score d'incertitude au seuil0,010

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0020,001
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0010,001
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0010,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,001
Charge utile insuffisante (le modèle a refusé de juger)0,0020,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,106
Tête enseignante GPT0,402
Écart entre enseignants0,296 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeEssai randomisé
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations3
Publié2021
Routes d'admission1
Résumé présentoui

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