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ARRY-371797 治疗扩张型心肌病及基因突变患者的安全性和有效性研究的简明报告

Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty gene.

机构信息

Brigham & Women's Hospital, Cardiovascular Medicine, Boston, MA, USA.

University of Colorado, Department of Medicine, Adult Medical Genetics Program, Aurora, CO, USA.

出版信息

Future Cardiol. 2023 Feb;19(2):55-63. doi: 10.2217/fca-2022-0099. Epub 2023 Jan 31.

DOI:10.2217/fca-2022-0099
PMID:36718638
Abstract

WHAT IS THIS PLAIN LANGUAGE SUMMARY ABOUT?: This plain language summary describes the results of a study looking at the effects of a medicine called ARRY-371797 (also known as PF-07265803) in people with dilated cardiomyopathy (DCM for short) caused by a faulty gene. This condition is called LMNA-related DCM. DCM happens when the heart becomes bigger and weaker than normal, impacting functional capacity and leading to symptoms of heart failure. This means the heart is not able to pump blood around the body as easily, and people are unable to do as much in their daily lives (like getting dressed and going shopping). People may inherit a faulty gene from one of their parents, or a faulty gene may develop when mistakes happen during cell growth and replication. ARRY-371797 targets a specific mechanism in the body that can lead to heart problems in people with a faulty gene. As ARRY-371797 is not currently approved for use outside of clinical trials, it doesn't currently have an easily recognizable trade name.

WHAT WERE THE RESULTS?: 12 American people (average age 50 years) with LMNA-related DCM took part in the study and received 400 mg or 100 mg of ARRY-371797 twice daily for 48 weeks. People knew which dose of ARRY-371797 they were taking. People were checked after 4, 12, 24, 36 and 48 weeks of taking ARRY-371797 to see how far they could walk in the 6-minute walk test (6MWT for short). The level of NT-proBNP in their blood was also measured. NT-proBNP is a biomarker used to measure the severity of heart failure. A biomarker is something found in the body that can be measured to indicate the extent of a disease. -After taking ARRY-371797 for 12 weeks, people were able to walk further in the 6MWT and had lower levels of NT-proBNP in their blood. This suggests improvement in functional capacity (exercise tolerance) and heart function. Researchers also asked people about their quality of life using the Kansas City Cardiomyopathy Questionnaire (KCCQ for short), and looked for any side effects. -Researchers saw some improvement in KCCQ scores. -Researchers saw no major side effects that they considered to be related to ARRY-371797 treatment. A side effect is something that people feel was caused by a medicine or treatment. Overall, this study showed that people with LMNA-related DCM who took ARRY-371797 had improved functional capacity (exercise tolerance), improved heart function, and improved quality of life. Phase 2 study (NCT02057341) Phase 2 long-term extension study (NCT02351856) Phase 3 REALM-DCM study (NCT03439514).

摘要

这篇通俗易懂的概要描述了一项研究的结果,该研究旨在观察一种名为 ARRY-371797(也称为 PF-07265803)的药物对由错误基因引起的扩张型心肌病(简称 DCM)患者的影响。这种情况被称为 LMNA 相关的 DCM。当心脏变得比正常情况下更大、更弱时,就会发生 DCM,这会影响功能能力并导致心力衰竭的症状。这意味着心脏不能像平时那样轻松地将血液泵送到全身,人们在日常生活中也不能做太多事情(例如穿衣服和购物)。人们可能会从父母一方遗传到一个错误的基因,或者在细胞生长和复制过程中发生错误时,也可能会产生一个错误的基因。 ARRY-371797 针对的是体内一种特定的机制,这种机制可能导致携带错误基因的人出现心脏问题。由于 ARRY-371797 目前尚未获得临床试验以外的批准使用,因此它目前没有一个易于识别的商品名。

结果如何?12 名患有 LMNA 相关 DCM 的美国人(平均年龄 50 岁)参与了这项研究,他们每天接受两次 400 毫克或 100 毫克的 ARRY-371797,持续 48 周。人们知道自己服用的 ARRY-371797 剂量。在服用 ARRY-371797 4、12、24、36 和 48 周后,对人们进行了检查,以了解他们在 6 分钟步行测试(简称 6MWT)中能走多远。他们血液中的 NT-proBNP 水平也进行了测量。NT-proBNP 是一种用于衡量心力衰竭严重程度的生物标志物。生物标志物是指可以在体内测量到的物质,用于表明疾病的严重程度。 -在服用 ARRY-371797 12 周后,人们在 6MWT 中能够走得更远,血液中的 NT-proBNP 水平也更低。这表明他们的功能能力(运动耐量)和心脏功能得到了改善。研究人员还使用堪萨斯城心肌病问卷(简称 KCCQ)询问了人们的生活质量,并寻找任何副作用。 -研究人员发现 KCCQ 评分有所提高。 -研究人员没有发现他们认为与 ARRY-371797 治疗相关的重大副作用。副作用是指人们认为是由药物或治疗引起的身体不适。总的来说,这项研究表明,服用 ARRY-371797 的 LMNA 相关 DCM 患者的功能能力(运动耐量)得到了改善,心脏功能得到了改善,生活质量得到了提高。2 期研究(NCT02057341)2 期长期扩展研究(NCT02351856)3 期 REALM-DCM 研究(NCT03439514)。

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引用本文的文献

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Characterization and natural history of patients with LMNA-related dilated cardiomyopathy in the phase 3 REALM-DCM trial.在3期REALM-DCM试验中,与LMNA相关的扩张型心肌病患者的特征及自然病史
ESC Heart Fail. 2024 Dec;11(6):4201-4208. doi: 10.1002/ehf2.14955. Epub 2024 Aug 15.