McDowell P Jane, Busby John, Stone John H, Butler Claire A, Heaney Liam G
Wellcome-Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry, and Biological Sciences, Queen's University Belfast, Belfast, United Kingdom; Department of Respiratory Medicine, Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, United Kingdom.
Centre for Public Health, School of Medicine, Dentistry, and Biological Sciences, Queen's University Belfast, Belfast, United Kingdom.
J Allergy Clin Immunol Pract. 2025 Feb;13(2):298-307.e10. doi: 10.1016/j.jaip.2024.10.024. Epub 2024 Oct 29.
Toxicities associated with oral corticosteroids (OCS) are well described. Targeted biologics for severe asthma (SA) substantially reduce OCS exposure with the potential to reduce cumulative OCS-related toxicities. The Glucocorticoid Toxicity Index (GTI) systematically assesses OCS-related toxicity; the GTI Aggregate Improvement Score (AIS) is a bidirectional measure of total toxicity change with a minimal clinically important difference (MCID) of ≤-10.
This study was a longitudinal assessment of patients with SA treated with biologic therapies to assess the trajectory of OCS-related toxicity and predictors of toxicity improvement.
A total of 89 patients with SA had GTI assessments at baseline and after 1 and 3 years of biologic therapy.
At 3 years, daily prednisolone use continued to decrease (6.9 mg/day [4.0, 9.4] year 1 vs 0.8 mg/day [0.0, 3.7] year 3, P < .001), OCS-related toxicity continued to decline (AIS at 3 years -36 [-94, 19]), and 61% (54 of 89) met the AIS MCID. There was a significant positive correlation between toxicity outcomes at years 1 and 3 (ρ 0.65, P < .001). Nearly half (49%) met the AIS MCID at both years 1 and 3, but 29% of the cohort did not meet the AIS MCID at either time point. Toxicity change at year 1 was predictive of toxicity change at year 3 for 79%. Toxicity reduction was not proportional to OCS reduction; there were no prebiologic characteristics that predicted toxicity reduction.
After 3 years of biologic treatment, 61% of patients with SA had clinically significant toxicity improvement. Individual toxicity outcomes at year 1 are associated with longitudinal outcomes, suggesting that for some, additional interventions are needed alongside OCS reduction to decrease morbidity.
与口服糖皮质激素(OCS)相关的毒性已得到充分描述。用于重度哮喘(SA)的靶向生物制剂可大幅减少OCS暴露,有可能降低累积的OCS相关毒性。糖皮质激素毒性指数(GTI)系统评估OCS相关毒性;GTI综合改善评分(AIS)是总毒性变化的双向指标,最小临床重要差异(MCID)为≤ -10。
本研究对接受生物治疗的SA患者进行纵向评估,以评估OCS相关毒性的变化轨迹及毒性改善的预测因素。
共有89例SA患者在基线以及生物治疗1年和3年后进行了GTI评估。
在3年时,泼尼松龙的每日用量持续下降(第1年为6.9毫克/天[4.0, 9.4],第3年为0.8毫克/天[0.0, 3.7],P <.001),OCS相关毒性持续下降(3年时的AIS为 -36 [-94, 19]),61%(89例中的54例)达到了AIS的MCID。第1年和第3年的毒性结果之间存在显著正相关(ρ 0.65,P <.001)。近一半(49%)在第1年和第3年都达到了AIS的MCID,但29%的队列在两个时间点都未达到AIS的MCID。第1年的毒性变化可预测79%的第3年毒性变化。毒性降低与OCS减少不成比例;没有生物治疗前的特征可预测毒性降低。
生物治疗3年后,61%的SA患者在临床上有显著的毒性改善。第1年的个体毒性结果与纵向结果相关,这表明对于一些患者,除了减少OCS外,还需要额外的干预措施以降低发病率。