A plain language summary of results from the LAVENDER study: trofinetide treatment for Rett syndrome

J. Neul, A. Percy, T. Benke, E. Berry-Kravis, D. Glaze, V. Abler, Tim T Z Lin, Kathie M Bishop, J. Youakim
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Abstract

This is a summary of an article about the LAVENDER study, which was published in Nature Medicine in June 2023. The study involved girls and young women with a rare genetic condition called Rett syndrome, which affects the way the brain develops. Researchers wanted to find out if a drug called trofinetide could improve the symptoms of Rett syndrome. A total of 187 girls and young women took trofinetide (brand name DAYBUE™) liquid or a placebo (something that looks the same as the trofinetide liquid but does not contain medicine) 2 times a day either by drinking it or through a tube into the stomach called a gastrostomy tube (g-tube). Changes in Rett syndrome symptoms were looked for by study doctors for 12 weeks by using a rating scale called the Clinical Global Impression–Improvement (CGI–I) and by caregivers (usually a parent) who completed a questionnaire called the Rett Syndrome Behaviour Questionnaire (RSBQ). Caregivers were also asked to rate communication and social interaction skills, which resulted in the ‘Social Composite’ score on a questionnaire called the Communication and Symbolic Behavior Scales Developmental Profile™ Infant–Toddler (CSBS-DP-IT) checklist. After 12 weeks of treatment, girls and young women who received trofinetide had greater improvements in their symptoms than those who took the placebo, as rated by the RSBQ and CGI–I. Participants who took trofinetide could communicate better than participants who took the placebo as rated on the CSBS–DP–IT Social Composite scale. The differences between trofinetide and the placebo were statistically significant, which means that it was unlikely that the benefit seen with trofinetide was caused by chance. The most common side effects in the trofinetide group were diarrhea (frequent watery bowel movements) and vomiting, and in almost all cases these were mild or moderate. In the LAVENDER study, trofinetide helped girls and young women with Rett syndrome by improving several important symptoms. This is the first study to show that a medicine, trofinetide, improves the symptoms of Rett syndrome. Clinical Trial Registration: NCT04181723 (LAVENDER) ( ClinicalTrials.gov )
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薰衣草研究结果的简单语言总结:特罗非肽治疗Rett综合征
这是2023年6月发表在《自然医学》杂志上的一篇关于LAVENDER研究的文章的摘要。该研究涉及患有一种名为Rett综合征的罕见遗传疾病的女孩和年轻女性,这种疾病会影响大脑的发育方式。研究人员想找出一种叫做trofinetide的药物是否能改善Rett综合征的症状。共有187名女孩和年轻女性每天服用2次trofinetide(品牌名DAYBUE™)液体或安慰剂(看起来与trofinetide液体相同但不含药物),要么通过饮用,要么通过胃造口管(g-tube)进入胃。研究医生使用临床整体印象改善量表(CGI-I)和照料者(通常是父母)在12周内完成一份名为Rett综合征行为问卷(RSBQ)的调查问卷,来观察Rett综合征症状的变化。照顾者还被要求对沟通和社会互动技能进行评分,这在一份名为“沟通和符号行为量表发展档案™婴幼儿(CSBS-DP-IT)”的问卷调查中得出了“社会综合”分数。经过12周的治疗,根据RSBQ和CGI-I的评分,接受trofinetide的女孩和年轻女性的症状比服用安慰剂的女孩和年轻女性有更大的改善。在CSBS-DP-IT社会综合量表中,服用trofinetide的参与者比服用安慰剂的参与者能够更好地沟通。trofinetide和安慰剂之间的差异在统计学上是显著的,这意味着trofinetide的益处不太可能是偶然引起的。在trofinetide组中最常见的副作用是腹泻(频繁的水样排便)和呕吐,而且在几乎所有的病例中,这些副作用都是轻微或中度的。在LAVENDER研究中,trofinetide通过改善几个重要症状来帮助患有Rett综合征的女孩和年轻女性。这是第一项研究表明,一种名为trofinetide的药物可以改善Rett综合征的症状。临床试验注册:NCT04181723 (LAVENDER) (ClinicalTrials.gov)
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