Department of Biostatistics, University of Washington, Seattle, WA, United States.
Clinical Learning, Evidence, and Research Center, University of Washington, Seattle, WA, United States.
Pain. 2023 Apr 1;164(4):811-819. doi: 10.1097/j.pain.0000000000002768. Epub 2022 Aug 26.
Conventional "1-variable-at-a-time" analyses to identify treatment effect modifiers are often underpowered and prone to false-positive results. This study used a "risk-modeling" approach guided by the Predictive Approaches to Treatment effect Heterogeneity (PATH) Statement framework: (1) developing and validating a multivariable model to estimate predicted future back-related functional limitations as measured by the Roland-Morris Disability Questionnaire (RMDQ) and (2) stratifying patients from a randomized controlled trial (RCT) of lumbar epidural steroid injections (LESIs) for the treatment of lumbar spinal stenosis into subgroups with different individualized treatment effects on RMDQ scores at the 3-week follow-up. Model development and validation were conducted in a cohort (n = 3259) randomly split into training and testing sets in a 4:1 ratio. The model was developed in the testing set using linear regression with least absolute shrinkage and selection regularization and 5-fold cross-validation. The model was then applied in the testing set and subsequently in patients receiving the control treatment in the RCT of LESI. R2 values in the training set, testing set, and RCT were 0.38, 0.32, and 0.34, respectively. There was statistically significant modification ( P = 0.03) of the LESI treatment effect according to predicted risk quartile, with clinically relevant LESI treatment effect point estimates in the 2 quartiles with greatest predicted risk (-3.7 and -3.3 RMDQ points) and no effect in the lowest 2 quartiles. A multivariable risk-modeling approach identified subgroups of patients with lumbar spinal stenosis with a clinically relevant treatment effect of LESI on back-related functional limitations.
传统的“逐一变量”分析方法通常无法识别治疗效果的调节剂,并且容易出现假阳性结果。本研究采用了一种“风险建模”方法,该方法以预测治疗效果异质性的方法学声明(Predictive Approaches to Treatment effect Heterogeneity,PATH)框架为指导:(1)制定和验证一个多变量模型,以估计未来由 Roland-Morris 残疾问卷(Roland-Morris Disability Questionnaire,RMDQ)测量的与背部相关的功能限制;(2)将接受腰椎硬膜外类固醇注射(Epidural Steroid Injections,ESIs)治疗腰椎管狭窄症的随机对照试验(Randomized Controlled Trial,RCT)的患者分层为不同的亚组,这些亚组在 3 周随访时的 RMDQ 评分有不同的个体化治疗效果。模型的制定和验证是在一个队列(n = 3259)中进行的,该队列按照 4:1 的比例随机分为训练集和测试集。在测试集中,使用带有最小绝对值收缩和选择规则(Least Absolute Shrinkage and Selection Operator,LASSO)的线性回归和 5 折交叉验证来开发模型。然后,在测试集中应用该模型,接着应用于接受 RCT 中 ESIs 对照治疗的患者。在训练集、测试集和 RCT 中的 R2 值分别为 0.38、0.32 和 0.34。根据预测风险四分位数,ESIs 治疗效果存在统计学显著的修饰(P = 0.03),在预测风险最高的 2 个四分位数中存在显著的 ESIs 治疗效果点估计(-3.7 和-3.3 RMDQ 点),而在预测风险最低的 2 个四分位数中没有效果。多变量风险模型确定了具有腰椎管狭窄症的患者亚组,ESIs 对与背部相关的功能限制具有临床相关的治疗效果。