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使用多种基于锚定和分布的估计方法来评估癌症治疗-生物反应调节剂功能评估(FACT-BRM)工具上具有临床意义的变化。

Using multiple anchor- and distribution-based estimates to evaluate clinically meaningful change on the Functional Assessment of Cancer Therapy-Biologic Response Modifiers (FACT-BRM) instrument.

作者信息

Yost Kathleen J, Sorensen Mark V, Hahn Elizabeth A, Glendenning G Alastair, Gnanasakthy Ari, Cella David

机构信息

Center on Outcomes, Research and Education (CORE), Evanston, IL 60201, USA.

出版信息

Value Health. 2005 Mar-Apr;8(2):117-27. doi: 10.1111/j.1524-4733.2005.08202.x.

DOI:10.1111/j.1524-4733.2005.08202.x
PMID:15804320
Abstract

OBJECTIVE

The interpretation of health-related quality of life (HRQL) data from clinical trials can be enhanced by understanding the degree of change in HRQL scores that is considered meaningful. Our objectives were to combine distribution-based and two anchor-based approaches to identify minimally important differences (MIDs) for the 27-item Trial Outcome Index (TOI), the seven-item Social Well-Being (SWB) subscale, and the six-item Emotional Well-being (EWB) subscale from the Functional Assessment of Cancer Therapy-Biological Response Modifiers (FACT-BRM) instrument.

METHODS

Distribution-based MIDs were based on the standard error of measurement. Anchor-based approaches utilized patient-reported global rating of change (GRC) and change in physician-reported performance status rating (PSR). Correlations and weighted kappa statistics were used to assess association and agreement between the two anchors. FACT-BRM changes were evaluated for three time periods: baseline to month 1, month 2 to month 3, and month 5 to month 6.

RESULTS

Association between GRC and change in PSR was poor. Correlation between the anchors and HRQL change scores was largest at month 1 and decreased through month 6. Combining results from all approaches, the MIDs identified were 5-8 points for the TOI, 2 points for the SWB subscale, and 2-3 points for the EWB subscale.

CONCLUSIONS

We combined patient-reported estimates, physician-reported estimates, and distribution-based estimates to derive MIDs for HRQL outcomes from the FACT-BRM. These results will enable interpretation of treatment group effects in a clinical trial setting, and they can be used to estimate sample size or power when designing future studies.

摘要

目的

通过了解被认为有意义的健康相关生活质量(HRQL)评分变化程度,可增强对临床试验中HRQL数据的解读。我们的目标是结合基于分布的方法和两种基于锚定的方法,来确定癌症治疗生物反应调节剂功能评估(FACT - BRM)工具中27项试验结果指数(TOI)、7项社会幸福感(SWB)子量表和6项情绪幸福感(EWB)子量表的最小重要差异(MID)。

方法

基于分布的MID基于测量标准误差。基于锚定的方法利用患者报告的总体变化评分(GRC)和医生报告的性能状态评分(PSR)变化。相关性和加权kappa统计量用于评估两个锚定之间的关联和一致性。在三个时间段评估FACT - BRM变化:基线至第1个月、第2个月至第3个月以及第5个月至第6个月。

结果

GRC与PSR变化之间的关联较差。锚定与HRQL变化评分之间的相关性在第1个月时最大,并在第6个月时下降。综合所有方法的结果,确定的TOI的MID为5 - 8分,SWB子量表为2分,EWB子量表为2 - 3分。

结论

我们结合了患者报告的估计值、医生报告的估计值和基于分布的估计值,以得出FACT - BRM中HRQL结果的MID。这些结果将有助于在临床试验环境中解释治疗组效应,并且在设计未来研究时可用于估计样本量或检验效能。

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