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在 2/3 期临床试验中尼曼-匹克 C1 临床严重程度量表的独立评估者之间具有高度一致性。

Consistently High Agreement Between Independent Raters of Niemann-Pick Type C1 Clinical Severity Scale in Phase 2/3 Trial.

机构信息

Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

出版信息

Pediatr Neurol. 2022 Feb;127:32-38. doi: 10.1016/j.pediatrneurol.2021.11.009. Epub 2021 Nov 29.

Abstract

BACKGROUND

Niemann-Pick disease, type C1 (NPC1) is a rare neurodegenerative genetic disorder characterized by impaired intracellular transport of cholesterol and other lipids. The Niemann-Pick Disease, type C1 Severity Scale (NPC-SS) was developed to quantify neurological progression of NPC; it is used to monitor the natural history of disease progression and assess response to treatment. The objective of the study was to examine the interrater reliability of the NPC-SS in a phase 2/3 trial.

METHODS

Study data were from a multicenter, prospective, randomized, double-blind trial of adrabetadex in 56 subjects with NPC1. Clinical data recorded at each study site were distributed to two independent blinded central raters to generate a severity score. A composite four-item score was utilized as the primary clinical study end point, whereas a five-item focused score has been utilized in other NPC1 trials. Interrater reliability was assessed using two-way mixed models for instrument stability, Cohen kappa, weighted kappa, and percent agreement for the four- and five-item scores.

RESULTS

The frequency distribution and mean (S.D.) of the NPC-SS domain assessments by the raters were almost identical. Evaluation at the patient visit level showed wide variability between visits; however, weighted kappa calculation provided a lower variability between visits. The average kappa coefficients ranged between 0.69 and 0.89, indicating good to very good agreement between raters.

CONCLUSIONS

These results support the NPC-SS, including derived four- and five-item composite scores, as reliable measures for use in a clinical trial setting.

摘要

背景

尼曼-匹克病 C1 型(NPC1)是一种罕见的神经退行性遗传疾病,其特征是胆固醇和其他脂质的细胞内转运受损。尼曼-匹克病 C1 严重程度评分(NPC-SS)是为了量化 NPC 的神经进展而开发的;它用于监测疾病进展的自然史并评估对治疗的反应。本研究的目的是在 2/3 期试验中检查 NPC-SS 的评分者间可靠性。

方法

研究数据来自 56 例 NPC1 患者接受 adrabetadex 的多中心、前瞻性、随机、双盲试验。每个研究地点记录的临床数据分发给两名独立的盲法中心评分者,以生成严重程度评分。四项综合评分被用作主要的临床研究终点,而在其他 NPC1 试验中使用了五项重点评分。使用双向混合模型评估仪器稳定性、Cohen kappa、加权 kappa 和四项和五项评分的百分比一致性来评估评分者间可靠性。

结果

评分者的 NPC-SS 域评估的频率分布和平均值(S.D.)几乎相同。在患者就诊水平的评估显示就诊之间存在很大的差异;然而,加权 kappa 计算提供了就诊之间更低的差异。平均kappa 系数在 0.69 到 0.89 之间,表明评分者之间具有良好到非常好的一致性。

结论

这些结果支持 NPC-SS,包括衍生的四项和五项综合评分,作为临床试验中可靠的测量工具。

相似文献

本文引用的文献

7
Niemann-Pick disease type C.尼曼-匹克病 C 型。
Orphanet J Rare Dis. 2010 Jun 3;5:16. doi: 10.1186/1750-1172-5-16.

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