From NYU Multiple Sclerosis Comprehensive Care Center (L.Z.R., I.K.), New York; Division of Biostatistics (X.L., J.D.G.), New York University School of Medicine; and Rocky Mountain MS Research Group (T.H., A.C., R.R.M., J.F.), Salt Lake City, UT.
Neurol Neuroimmunol Neuroinflamm. 2020 Feb 4;7(2). doi: 10.1212/NXI.0000000000000672. Print 2020 Mar.
To determine if the concentration and saturation of natalizumab (NTZ) administration at extended interval dosing (EID; every 5-8 weeks) over 18 months is able to be maintained in the range considered adequate to sustain the clinical efficacy of NTZ.
In a cross-sectional assessment of patients with multiple sclerosis (MS) who received standard interval dosing (every 4 weeks) or EID, serum NTZ concentrations were measured using ELISA, and α-integrin receptor saturations were analyzed via cytometry, in blood samples obtained at trough timepoints.
Trough serum concentration was above the "therapeutic" concentration of 2.0 μg/mL in 72% of EID patients. Trough saturation was above the "therapeutic" 50% threshold in 79% of EID-treated patients. Our model predicted that at least 9 NTZ infusions/year are required to maintain adequate trough saturation and concentration levels. Higher body mass index (BMI) was a predictor of suboptimal trough saturation on EID NTZ.
Trough α4-integrin receptor saturation >50% correlated with high clinical efficacy of NTZ in previous studies. A continual treatment with EID maintains receptor saturation and concentration that are in the "therapeutic range" for most patients. This finding provides biological plausibility for the clinical efficacy of NTZ EID. Patients with higher BMI may require closer clinical and MRI follow-up.
确定在 18 个月的时间内,每隔延长时间(EID;每 5-8 周)给药时,那他珠单抗(NTZ)的浓度和饱和度是否能够维持在被认为足以维持 NTZ 临床疗效的范围内。
在一项对接受标准间隔给药(每 4 周)或 EID 的多发性硬化症(MS)患者的横断面评估中,使用 ELISA 测量血清 NTZ 浓度,并通过细胞术分析 α-整合素受体饱和度,在获得的血样中在谷值时间点。
EID 患者中 72%的谷值血清浓度高于 2.0 μg/mL 的“治疗”浓度。79%的 EID 治疗患者的谷值饱和度超过 50%的“治疗”阈值。我们的模型预测,至少需要 9 次 NTZ 输注/年才能维持足够的谷值饱和度和浓度水平。较高的体重指数(BMI)是 EID NTZ 谷值饱和度不理想的预测因素。
以前的研究表明,α4-整合素受体饱和度>50%与 NTZ 的高临床疗效相关。持续的 EID 治疗可维持受体饱和度和浓度处于大多数患者的“治疗范围”内。这一发现为 NTZ EID 的临床疗效提供了生物学上的合理性。BMI 较高的患者可能需要更密切的临床和 MRI 随访。