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接受 voxotor 治疗的镰状细胞病儿童和成人的患者报告体验:一项半结构化访谈研究。

Patient-Reported Experiences in Voxelotor-Treated Children and Adults with Sickle Cell Disease: A Semistructured Interview Study.

机构信息

Aflac Cancer & Blood Disorders Center of Children's Healthcare of Atlanta and Department of Pediatrics, Emory University, Atlanta, GA, USA.

UT Physicians Comprehensive Sickle Cell Center, The University of Texas Health Science Center at Houston, Houston, TX, USA.

出版信息

Biomed Res Int. 2023 Jan 28;2023:7533111. doi: 10.1155/2023/7533111. eCollection 2023.

Abstract

OBJECTIVE

Voxelotor is a first-in-class sickle hemoglobin-polymerization inhibitor that was approved in 2019 by the US Food and Drug Administration for treatment of patients with sickle cell disease (SCD) aged ≥12 years; in 2021, the approval was extended to children with SCD aged 4 to 11 years. Additionally, both the Ministry of Health and Prevention for the United Arab Emirates and the European Commission granted marketing authorization for voxelotor in September 2021 and February 2022, respectively, for treatment of SCD in adults and pediatric patients aged ≥12 years. Thus, additional information on the patient experience with voxelotor would be useful for patients, caregivers, and healthcare professionals alike. The purpose of this study was to conduct semistructured interviews in an effort to understand the experiences and perspectives of voxelotor-treated patients with SCD.

METHODS

One-time semistructured interviews with adults, adolescents, and children with SCD and their primary caregivers were conducted in the United States. Twenty-three adults and adolescents were recruited across 4 clinical sites, and 10 children-caregiver dyads were recruited from a single site. The interview was designed to elicit patient perspectives on symptomatic changes with voxelotor and the impact of treatment on patients' perceived health-related quality of life. Individual interview transcripts were analyzed using a thematic analytic approach, and concept saturation was assessed in both cohorts.

RESULTS

Most patients reported improvements in their SCD symptoms with voxelotor treatment, specifically regarding pain crises, jaundice, and fatigue. Almost all patients experienced improvements in self-reported health-related quality of life with voxelotor treatment.

CONCLUSIONS

This study provides patient and caregiver perspectives on the symptomatic benefits of voxelotor treatment. These findings not only highlight the benefits of voxelotor treatment in improving symptoms and increasing health-related quality of life across the entire SCD population but also can inform further research on SCD-specific patient-reported outcomes.

摘要

目的

沃瑟罗特是一种首创的镰状血红蛋白聚合抑制剂,于 2019 年被美国食品和药物管理局批准用于治疗 12 岁及以上的镰状细胞病(SCD)患者;2021 年,批准范围扩大到 4 至 11 岁的 SCD 儿童。此外,阿拉伯联合酋长国卫生部和预防部以及欧洲委员会分别于 2021 年 9 月和 2022 年 2 月授予沃瑟罗特在成人和 12 岁及以上儿科患者中治疗 SCD 的营销授权。因此,了解患者对沃瑟罗特的治疗体验的更多信息,对患者、护理人员和医疗保健专业人员都将是有用的。本研究旨在进行半结构化访谈,以了解接受沃瑟罗特治疗的 SCD 患者的体验和观点。

方法

在美国对 SCD 成人、青少年和儿童及其主要护理人员进行一次性半结构化访谈。在 4 个临床地点招募了 23 名成人和青少年,在一个临床地点招募了 10 名儿童-护理人员二人组。访谈旨在了解患者对沃瑟罗特治疗相关症状变化的看法,以及治疗对患者感知健康相关生活质量的影响。使用主题分析方法对个人访谈记录进行分析,并在两个队列中评估概念饱和度。

结果

大多数患者报告称,沃瑟罗特治疗后 SCD 症状有所改善,特别是疼痛发作、黄疸和疲劳。几乎所有患者都报告称,沃瑟罗特治疗后健康相关生活质量有所改善。

结论

本研究提供了患者和护理人员对沃瑟罗特治疗症状获益的看法。这些发现不仅强调了沃瑟罗特治疗在改善整个 SCD 人群的症状和提高健康相关生活质量方面的益处,而且还可以为进一步研究 SCD 特定的患者报告结局提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/feed/9899137/91199e1d06e1/BMRI2023-7533111.001.jpg

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