首页> 外文期刊>Journal of Clinical Epidemiology >A combination of distribution- and anchor-based approaches determined minimally important differences (MIDs) for four endpoints in a breast cancer scale.
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A combination of distribution- and anchor-based approaches determined minimally important differences (MIDs) for four endpoints in a breast cancer scale.

机译:基于分布和基于锚的方法的组合确定了乳腺癌量表中四个端点的最小重要差异(MID)。

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OBJECTIVE: To determine distribution- and anchor-based minimal important difference (MID) estimates for four scores from the Functional Assessment of Cancer Therapy-Breast (FACT-B): the breast cancer subscale (BCS), Trial Outcome Index (TOI), FACT-G (the general version), and FACT-B. STUDY DESIGN AND SETTING: We used data from a Phase III clinical trial in metastatic breast cancer (ECOG study 1193; n=739) and a prospective observational study of pain in metastatic breast cancer (n=129). One third and one half of the standard deviation and 1 standard error of measurement were used as distribution-based criteria. Clinical indicators used to determine anchor-based differences included ECOG performance status, current pain, and response to treatment. RESULTS: FACT-B scores were responsive to performance status and pain anchors, but not to treatment response. By combining the results of distribution- and anchor-based methods, MID estimates were obtained: BCS=2-3 points, TOI=5-6 points, FACT-G=5-6 points, and FACT-B=7-8 points. CONCLUSION: Distribution- and anchor-based estimates of the MID do show convergence. These estimates can be used in combination with other measures of efficacy to determine meaningful benefit and provide a basis for sample size estimation in clinical trials.
机译:目的:根据乳腺癌的功能评估(FACT-B)中的四个得分,确定基于分布和锚的最小重要差异(MID)估算值:乳腺癌子量表(BCS),试验结果指数(TOI), FACT-G(通用版本)和FACT-B。研究设计和设置:我们使用了转移性乳腺癌的III期临床试验数据(ECOG研究1193; n = 739)和转移性乳腺癌疼痛的前瞻性观察性研究(n = 129)。标准偏差的三分之一和一半和测量的1个标准误差用作基于分布的标准。用于确定基于锚的差异的临床指标包括ECOG表现状态,当前疼痛和对治疗的反应。结果:FACT-B评分对表现状态和疼痛锚定有反应,但对治疗反应无​​反应。通过结合基于分布和基于锚的方法的结果,获得了MID估计值:BCS = 2-3点,TOI = 5-6点,FACT-G = 5-6点和FACT-B = 7-8点。结论:基于分布和锚的MID估计确实显示出收敛性。这些估计值可以与其他功效度量结合使用,以确定有意义的收益,并为临床试验中的样本量估计提供基础。

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