The patient experience of CHAPLE disease: results from interviews conducted as part of a clinical trial for an ultra-rare condition.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Leighann Litcher-Kelly, Ahmet Ozen, Sarah Ollis, Hagit Baris Feldman, Andrew Yaworsky, Paolo Medrano, Voranush Chongsrisawat, Lorah Perlee, Marisa Walker, Sharanya Pradeep, Diane M Turner-Bowker, Alina Kurolap, Orly Eshach Adiv, Michael J Lenardo, Olivier A Harari, Jessica J Jalbert
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引用次数: 0

Abstract

Background: CD55 deficiency with hyper-activation of complement, angiopathic thrombosis, and protein-losing enteropathy (CHAPLE) disease is a newly identified condition with an estimated worldwide prevalence of < 100 patients. Patient interviews can ensure that what is important to patients is assessed in a clinical trial program. Due to the rare and potentially fatal nature of CHAPLE disease, interviews were conducted as part of the pozelimab clinical trial, rather than in a separate study before the trial. The aim of the interviews was to identify the key disease-related signs, symptoms, and health-related quality-of-life (HRQoL) impacts that are important and relevant to patients with CHAPLE disease.

Methods: Interviews were conducted with patients and/or caregivers at two timepoints (screening and Week 24) during the pozelimab trial to document the signs/symptoms and HRQoL impacts of CHAPLE disease, and document the most bothersome sign/symptom at screening. At Week 24, interviews gathered additional information on the patient experience from caregivers and patients (note: the impact of pozelimab treatment was also collected, though these results are presented elsewhere).

Results: Ten patients, aged 3-19 years, were enrolled in the trial; caregivers contributed to nine interviews. Thirty-one signs‌/symptoms and 65 HRQoL impacts were reported during the interviews. Abdominal pain, diarrhea, facial and peripheral edema/‌swelling, nausea, and vomiting emerged as the core signs/‌symptoms of CHAPLE disease (i.e., experienced by ≥ 90% of patients prior to treatment). The remaining 25 signs/symptoms were experienced by four or fewer (n ≤ 4, ≤ 40.0%) patients, and 15 were only reported by one patient each. Abdominal pain and facial edema were reported as the most bothersome signs/‌symptoms (n = 9, 90.0% and n = 1, 10.0%, respectively). The most frequently reported (i.e., ≥ 80% of interviews) HRQoL impacts were restricted diet (n = 10, 100.0%), sleep disruptions (n = 10, 100.0%), missing school (n = 9, 90.0%), ability to get dressed independently (n = 8, 80.0%), and difficulty engaging in play activities (n = 8, 80.0%).

Conclusions: The main finding from these patient interviews is the identification of six core signs/symptoms of CHAPLE disease: abdominal pain, diarrhea, facial edema/swelling, peripheral edema/swelling, nausea, and vomiting. The severity of the core signs/symptoms leads to substantial impacts on patients' lives.

Trial registration: ClinicalTrials.gov, NCT04209634. Registered 20 December 2019 https://classic.

Clinicaltrials: gov/ct2/show/NCT04209634 .

CHAPLE疾病的患者经历:作为一种超罕见疾病临床试验的一部分进行的访谈结果。
背景:CD55缺乏症伴补体超激活、血管血栓形成和蛋白质丢失性肠病(CHAPLE)是一种新发现的疾病,估计在世界范围内流行。方法:在pozelimab试验期间,在两个时间点(筛查和第24周)对患者和/或护理人员进行访谈,以记录CHAPLE疾病的体征/症状和HRQoL影响,并记录筛查时最麻烦的体征/症状。在第24周,访谈从护理人员和患者那里收集了关于患者体验的额外信息(注意:也收集了pozelimab治疗的影响,尽管这些结果在其他地方呈现)。结果:10例患者入组,年龄3-19岁;护理人员参与了9个访谈。在访谈中报告了31个体征/症状和65个HRQoL影响。腹痛、腹泻、面部和周围水肿/肿胀、恶心和呕吐是CHAPLE疾病的核心体征/症状(即≥90%的患者在治疗前经历过这些症状)。其余25例体征/症状出现在4例或更少(n≤4,≤40.0%)患者中,15例仅出现在1例患者中。据报道,腹痛和面部水肿是最令人烦恼的体征/症状(n = 9,90.0%和n = 1,10.0%)。最常见的HRQoL影响报告(即≥80%的访谈)是限制饮食(n = 10, 100.0%)、睡眠中断(n = 10, 100.0%)、缺课(n = 9, 90.0%)、独立穿衣服能力(n = 8, 80.0%)和难以参与游戏活动(n = 8, 80.0%)。结论:这些患者访谈的主要发现是确定了CHAPLE疾病的六个核心体征/症状:腹痛、腹泻、面部水肿/肿胀、周围水肿/肿胀、恶心和呕吐。核心体征/症状的严重程度会对患者的生活产生重大影响。试验注册:ClinicalTrials.gov, NCT04209634。注册于2019年12月20日https://classic.Clinicaltrials: gov/ct2/show/NCT04209634。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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