Department of Surgical Oncology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Value Health. 2009 Nov-Dec;12(8):1144-50. doi: 10.1111/j.1524-4733.2009.00570.x. Epub 2009 Jun 25.
Minimal Important Differences (MIDs) establish benchmarks for interpreting mean differences in clinical trials involving quality of life outcomes and inform discussions of clinically meaningful change in patient status. The purpose of this study was to assess MIDs for the Functional Assessment of Cancer Therapy-Melanoma (FACT-M).
A prospective validation study of the FACT-M was performed with 273 patients with stages I through IV melanoma. FACT-M, Karnofsky Performance Scales, and Eastern Cooperative Oncology Group Performance Status scores were obtained at baseline and 3 months following enrollment. Anchor- and distribution-based methods for assessing MIDs were compared, and pattern-mixture modeling was employed to derive multivariate adjusted estimates.
This study indicates that an approximate range for MIDs of the FACT-M subscales is between 5 to 9 points for the Trial Outcome Index, 4 to 6 points for the Melanoma Combined Subscale, 2 to 4 points for the Melanoma Subscale, and 1 to 2 points for the Melanoma Surgery Subscale. Each method produced similar but not identical ranges of MIDs.
The properties of the anchor instrument employed to derive MIDs directly affect resulting MID ranges and point values. When MIDs are offered as supportive evidence of a clinically meaningful change, the anchor instrument used to derive clinically meaningful thresholds of change should be clearly stated along with information supporting the choice of anchor instrument as the most appropriate for the domain of interest.
最小有意义差异(MIDs)为解释涉及生活质量结果的临床试验中的均值差异提供了基准,并为患者状况的临床有意义变化提供了讨论依据。本研究的目的是评估癌症治疗-黑素瘤功能评估(FACT-M)的 MIDs。
对 273 例 I 期至 IV 期黑素瘤患者进行了 FACT-M 的前瞻性验证研究。在入组后 3 个月时获得了 FACT-M、卡诺夫斯基表现量表和东部合作肿瘤学组表现状态评分。比较了基于锚定和分布的 MIDs 评估方法,并采用模式混合建模方法得出了多变量校正的估计值。
本研究表明,FACT-M 子量表的 MIDs 近似范围为:试验结局指数约为 5 至 9 分,黑素瘤综合子量表为 4 至 6 分,黑素瘤子量表为 2 至 4 分,黑素瘤手术子量表为 1 至 2 分。每种方法都产生了相似但不完全相同的 MIDs 范围。
用于得出 MIDs 的锚定工具的特性直接影响到最终的 MID 范围和分值。当 MIDs 被作为临床有意义变化的支持证据时,应该明确说明用于得出临床有意义变化阈值的锚定工具,并提供支持选择最适合所关注领域的锚定工具的信息。