Concizumab prophylaxis in persons with hemophilia A or B with inhibitors: patient-reported outcome results from the phase 3 explorer7 study

IF 3.4 3区 医学 Q2 HEMATOLOGY
Huyen Tran , Sylvia von Mackensen , Aby Abraham , Giancarlo Castaman , Kingsley Hampton , Paul Knoebl , Silvia Linari , Jan Odgaard-Jensen , Jesper Skov Neergaard , Oleksandra Stasyshyn , Jay Jay Thaung Zaw , Bulent Zulfikar , Amy Shapiro
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Abstract

Background

Patient-reported outcomes (PROs) reflect patient perceptions of disease and treatment and are important for evaluating new therapies.

Objectives

Evaluate the effects of once-daily concizumab prophylaxis on health-related quality of life (HRQoL), treatment burden, and treatment preference in males aged ≥12 years with hemophilia A/B with inhibitors.

Methods

Patients enrolled in the multicenter, open-label explorer7 phase 3 study (ClinicalTrials.gov identifier: NCT04083781) were randomized to receive no prophylaxis (arm 1) or concizumab prophylaxis (arm 2) or were nonrandomly allocated to concizumab prophylaxis (arms 3 and 4). The study included questionnaires to assess patients’ perception of HRQoL (Haemophilia Quality of Life Questionnaire for Adults), treatment burden (Hemophilia Treatment Experience Measure), and treatment preference (Haemophilia Patient Preference Questionnaire).

Results

The estimated treatment difference between patients receiving concizumab prophylaxis vs no prophylaxis at week 24 for Haemophilia Quality of Life Questionnaire for Adults “total score” was −22.6 points (95% CI, −42.5; −2.7), directionally favoring patients receiving concizumab prophylaxis. For Hemophilia Treatment Experience Measure “total score,” the estimated treatment difference was −19.9 points (95% CI, −34.3, −5.6) in favor of concizumab vs no prophylaxis. The majority of patients receiving concizumab expressed a preference for concizumab over their previous treatment, the main reasons being “fewer bleeds,” “require less time,” and “less painful to inject.” Across all PROs, there were less responses collected than anticipated, limiting interpretations.

Conclusion

PROs collected during the explorer7 study showed improvements in some domains of HRQoL, treatment burden, and patient treatment preference in persons with hemophilia A or B with inhibitors receiving concizumab prophylaxis compared with no prophylaxis.

Abstract Image

抑制剂A型或B型血友病患者的康舒单抗预防治疗:Explorer7 第三阶段研究的患者报告结果
背景患者报告的结果(PROs)反映了患者对疾病和治疗的看法,对于评估新疗法非常重要。目的评估每日一次的康妥珠单抗预防性治疗对年龄≥12岁、患有血友病A/B并伴有抑制剂的男性患者的健康相关生活质量(HRQoL)、治疗负担和治疗偏好的影响。方法参加多中心、开放标签Explorer7 3期研究(ClinicalTrials.gov标识符:NCT04083781)的患者被随机分配到不接受预防治疗(第1组)或使用康珠单抗预防治疗(第2组),或非随机分配到使用康珠单抗预防治疗(第3组和第4组)。研究包括问卷调查,以评估患者的 HRQoL 感知(成人血友病生活质量问卷)、治疗负担(血友病治疗体验测量)和治疗偏好(血友病患者偏好问卷)。结果 第24周时,在成人血友病生活质量问卷 "总分 "方面,接受康妥珠单抗预防治疗与不接受预防治疗的患者之间的估计治疗差异为-22.6分(95% CI,-42.5;-2.7),方向上有利于接受康妥珠单抗预防治疗的患者。就血友病治疗体验测量(Hemophilia Treatment Experience Measure)"总分 "而言,估计治疗差异为-19.9分(95% CI,-34.3,-5.6),有利于接受康珠单抗与不接受预防治疗的患者。大多数接受康珠单抗治疗的患者表示,与之前的治疗方法相比,他们更倾向于使用康珠单抗,主要原因是 "出血更少"、"所需时间更短 "和 "注射痛苦更小"。结论Explorer7研究期间收集的PROs显示,与未接受预防性治疗相比,A型血友病或B型血友病抑制剂患者接受康利珠单抗预防性治疗后,在某些方面的HRQoL、治疗负担和患者治疗偏好都有所改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.60
自引率
13.00%
发文量
212
审稿时长
7 weeks
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