Ganju Jitendra
Ganju Clinical Trials, LLC, San Francisco, California, USA.
Pharm Stat. 2025 May-Jun;24(3):e70015. doi: 10.1002/pst.70015.
The term "minimal clinically important difference" (MCID), though defined as the smallest change in an outcome that is meaningful to the patient, is often used to interpret differences between treatment groups. It is in this context that the limitations of MCID are discussed, which include: the omission of the role of time in its definition for progressive diseases; the unsuitability of adopting MCID derived from open-label studies for randomized, placebo-controlled, blinded studies; the unreliability of MCID in rare disease trials; challenges in interpretation when placebo patients also achieve MCID; the failure to account for how differences in patient populations affect MCID (e.g., inclusion or exclusion of patients on prior treatment); not recognizing the connection between the true treatment effect, MCID and power; lack of consideration of differences in analysis methods (e.g., the extent of missing data and how it is handled); and the limitations of an MCID-based responder analysis. Therefore, the recommendation made is to prospectively define a customized MCID that addresses each deficit. If the deficits cannot be adequately resolved, then the recommendation is that trial results should be interpreted without reference to MCID.
“最小临床重要差异”(MCID)这一术语虽被定义为对患者有意义的结局方面的最小变化,但常被用于解释治疗组之间的差异。正是在这种背景下,人们讨论了MCID的局限性,其中包括:在其对进展性疾病的定义中忽略了时间因素;将来自开放标签研究的MCID用于随机、安慰剂对照、双盲研究并不合适;MCID在罕见病试验中不可靠;当安慰剂组患者也达到MCID时在解释方面存在挑战;未考虑患者群体差异如何影响MCID(例如,是否纳入接受过前期治疗的患者);未认识到真实治疗效果、MCID与检验效能之间的联系;未考虑分析方法的差异(例如,缺失数据的程度及其处理方式);以及基于MCID的反应者分析的局限性。因此,所提出的建议是前瞻性地定义一个针对每个缺陷的定制化MCID。如果这些缺陷无法得到充分解决,那么建议在解释试验结果时不参考MCID。