Henry Christopher N, Goldenholz Daniel M
Department of Neurology, Children's Hospital of Richmond at VCU Health, Virginia, United States.
Beth Israel Deaconess Medical Center, Department of Neurology, United States.
Ann Clin Transl Neurol. 2025 Oct;12(10):2130-2135. doi: 10.1002/acn3.70139. Epub 2025 Jul 21.
To quantify how often anti-seizure medications (ASMs) appear ineffective yet provide benefit when considering seizure frequency (SF) variability.
We used the CHOCOLATES seizure diary simulator to generate 100,000 patient seizure diaries that reflect natural SF variation in a heterogeneous population. Medication effect was modeled as a 20% average SF reduction (standard deviation 10%). We identified how many patients with an observed ≥ 25% SF increase (apparent worsening) actually had a true ≥ 10% SF reduction (vs. no medication), and how many with an observed ≥ 50% SF reduction (apparent responders) would have shown < 0% reduction if not taking the ASM. We also quantified how many individuals who had apparent worsening were actual worsening (> 0% SF increase vs. no medication).
Simulations closely matched real-world ASM trials, showing a median SF reduction of 36% with ASM versus 17% with placebo; 35% of patients on ASM achieved ≥ 50% SF reduction versus 20% on placebo. Apparent worsening occurred in 12%; among these, 76% were true improvers. Of the apparent responders, 12% were true nonresponders. Only 4% of the individuals with apparent worsening truly worsened compared to no medication.
SF variability can lead to significant misclassification of ASM benefit. Many patients labeled as having "failed" an ASM trial were likely receiving meaningful benefit and may warrant reconsideration of the medication. Prospective clinical studies are needed to determine how best to account for SF variability and refine the interpretation of treatment response in epilepsy management.
在考虑癫痫发作频率(SF)变异性的情况下,量化抗癫痫药物(ASM)看似无效但仍能带来益处的频率。
我们使用CHOCOLATES癫痫发作日记模拟器生成100,000份患者癫痫发作日记,以反映异质性人群中的自然SF变化。将药物疗效建模为平均SF降低20%(标准差10%)。我们确定了有多少观察到SF增加≥25%(明显恶化)的患者实际上有真正的SF降低≥10%(与未用药相比),以及有多少观察到SF降低≥50%(明显有反应)的患者如果未服用ASM会显示出<0%的降低。我们还量化了有多少看似恶化的个体实际上是病情恶化(与未用药相比SF增加>0%)。
模拟结果与现实世界中的ASM试验密切匹配,显示ASM治疗时SF中位数降低36%,而安慰剂治疗时为17%;接受ASM治疗的患者中有35%实现了SF降低≥50%,而接受安慰剂治疗的患者中这一比例为20%。明显恶化的情况发生在12%的患者中;在这些患者中,76%是真正的改善者。在明显有反应的患者中,12%是真正无反应者。与未用药相比,只有4%看似恶化的个体实际上病情真正恶化。
SF变异性可能导致对ASM益处的显著错误分类。许多被标记为ASM试验“失败”的患者可能正在获得有意义的益处,可能需要重新考虑用药。需要进行前瞻性临床研究,以确定如何最好地考虑SF变异性并完善癫痫管理中治疗反应的解读。