Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Md.
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Md; Department of Dermatology, Oregon Health & Science University, Portland, Ore.
J Allergy Clin Immunol Pract. 2018 Jan-Feb;6(1):190-195. doi: 10.1016/j.jaip.2017.06.006. Epub 2017 Jul 27.
Glucocorticoids (GCs) are considered first-line treatment for platelet-derived growth factor α (PDGFRA)-negative hypereosinophilic syndromes (HESs). Despite this, little is known about clinical predictors of GC responsiveness in HES.
Knowledge of clinical and laboratory predictors of GC response before initiation of GC could lead to more rational selection of subjects with HES for whom earlier institution of second-line and alternative therapies would be appropriate.
Response to GC, as defined by the reduction of the absolute eosinophil count to below 1000/mm and control of symptoms, was assessed by a retrospective chart review of subjects with PDGFRA-negative HES evaluated on an institutional review board-approved protocol. Demographic, clinical, and laboratory parameters obtained before institution of GC, as well as final diagnosis, were evaluated to determine predictors of GC response. Proportional odds models were used for univariate and multivariate assessment of predictors with permutation adjusted P values to correct for multiple comparisons.
A total of 164 subjects with PDGFRA-negative HES were categorized according to GC response. Of them, 39% of the subjects responded to low dose (≤10 mg) prednisone, 9% did not respond to GC, and the remainder (52%) had variable responses to GC. The HES subtype diagnosis was the best predictor of response to GC with myeloid forms and lymphocytic variants of HES being the least responsive to GC.
In a large cohort of well-characterized subjects with HES, the odds of response to GC was predicted by HES subtype. Using this model, clinicians may more readily proceed to second-line agents in subjects with confirmed lymphocytic or myeloid forms of HES.
糖皮质激素(GCs)被认为是血小板衍生生长因子α(PDGFRA)阴性嗜酸性粒细胞增多综合征(HES)的一线治疗药物。尽管如此,对于 HES 中 GC 反应的临床预测因素知之甚少。
在开始使用 GC 之前了解 GC 反应的临床和实验室预测因素,可能会导致更合理地选择 HES 患者,以便更早地为其提供二线和替代治疗。
通过回顾性审查机构审查委员会批准的方案评估的 PDGFRA 阴性 HES 患者的图表,评估 GC 反应,定义为绝对嗜酸性粒细胞计数降至 1000/mm 以下和症状控制。评估了在开始使用 GC 之前获得的人口统计学、临床和实验室参数,以及最终诊断,以确定 GC 反应的预测因素。使用比例优势模型进行单变量和多变量评估,并进行置换调整 P 值以校正多次比较。
根据 GC 反应,共对 164 例 PDGFRA 阴性 HES 患者进行了分类。其中,39%的患者对低剂量(≤10mg)泼尼松有反应,9%的患者对 GC 无反应,其余(52%)患者对 GC 有不同的反应。HES 亚型诊断是 GC 反应的最佳预测因素,骨髓形式和淋巴细胞变异型 HES 对 GC 的反应性最低。
在一组特征良好的 HES 患者中,GC 反应的可能性由 HES 亚型预测。使用该模型,临床医生可能更容易在确诊为淋巴细胞或骨髓形式的 HES 患者中使用二线药物。