Domingo Christian, Monserrate Daniel-Ross, Ollert Markus, Pomares Xavier, Forné Carles, Del Estal Jorge, Amengual María José
Department of Pulmonary Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, 08208 Sabadell, Barcelona, Spain.
Clinical Research Division of Molecular and Clinical Allergotoxicology, Department of Dermatology and Allergy, Technische Universität München, 80802 Münich, Germany.
Int J Mol Sci. 2025 Mar 21;26(7):2852. doi: 10.3390/ijms26072852.
To date, no biomarkers have been found that are able to predict the clinical response to omalizumab. The aim of this study was to assess whether blood concentration of free Immunoglobulin E (IgE) can predict response to treatment with this monoclonal antibody. In a group of patients who were candidates for omalizumab treatment, forced spirometry and blood IgE were measured at entry and at each six-month visit, and free-IgE blood concentrations were measured at month 6. At month 18, the OMADORE protocol was applied. The complete follow-up lasted 30 months. Patients were considered responders if they met at least one of the following criteria: increase in forced expiratory volume in one second (FEV) at the follow-up visit compared to baseline; reduction in corticosteroid dose at the last visit compared to baseline; reduction in omalizumab dose at the follow-up visit; a positive score on the composite index combining all three criteria. The biomarker used to predict treatment response was the free IgE value and the percentage of free IgE to total IgE measured at visit 1, after six months of omalizumab treatment. The percentage of responders varied according to the parameter used (FEV, omalizumab, corticosteroid dose, and the composite index; 45.2%, 64.5%, 48.4%, and 77.4%, respectively). IgE blockade was around 97% both for the group as a whole and for the subgroups. There were no differences in free IgE values nor in the ratio of free IgE to total IgE between responders and non-responders. These results confirm that there is a group of patients who may benefit from the reduction/withdrawal of omalizumab. Determination of free IgE six months after initiation of omalizumab treatment does not discriminate between responders and non-responders.
迄今为止,尚未发现能够预测奥马珠单抗临床反应的生物标志物。本研究的目的是评估游离免疫球蛋白E(IgE)的血药浓度是否能够预测这种单克隆抗体的治疗反应。在一组奥马珠单抗治疗候选患者中,在入组时及每6个月随访时测量用力肺活量和血IgE,并在第6个月时测量游离IgE血药浓度。在第18个月时,应用OMADORE方案。完整的随访持续30个月。如果患者符合以下至少一项标准,则被视为有反应者:与基线相比,随访时1秒用力呼气量(FEV)增加;与基线相比,最后一次随访时皮质类固醇剂量减少;随访时奥马珠单抗剂量减少;综合三项标准的综合指数得分呈阳性。用于预测治疗反应的生物标志物是在奥马珠单抗治疗6个月后的第1次随访时测量的游离IgE值以及游离IgE占总IgE的百分比。根据所使用的参数(FEV、奥马珠单抗、皮质类固醇剂量和综合指数),有反应者的比例各不相同(分别为45.2%、64.5%、48.4%和77.4%)。无论是整个组还是各亚组,IgE阻断率均约为97%。有反应者与无反应者之间的游离IgE值以及游离IgE与总IgE的比值均无差异。这些结果证实,有一组患者可能会从奥马珠单抗的减量/停药中获益。在奥马珠单抗治疗开始6个月后测定游离IgE并不能区分有反应者和无反应者。