奥马佐单抗
医学
内科学
血管性水肿
生物标志物
胃肠病学
D-二聚体
耐火材料(行星科学)
免疫球蛋白E
抗体
免疫学
生物化学
天体生物学
物理
化学
作者
Angelo Valerio Marzano,Giovanni Genovese,Giovanni Casazza,Maria Teresa Fierro,Paolo Dapavo,Nunzio Crimi,Silvia Mariel Ferrucci,Patrizia Pepe,Serena Liberati,Paolo D. Pigatto,Anna Maria Offidani,Emanuela Martina,Giampiero Girolomoni,Marco Rovaris,Caterina Foti,Luca Stingeni,Antonio Cristaudo,Giorgio Walter Canonica,Eustachio Nettis,Riccardo Asero
摘要
BACKGROUND: Chronic spontaneous urticaria (CSU) is defined as spontaneous occurrence of wheals and/or angioedema for ≥6 weeks. Omalizumab is a monoclonal anti-IgE antibody effective in refractory CSU, but its mechanism of action and markers predictive of response remain not completely defined. OBJECTIVES: To correlate baseline levels of two proposed biomarkers, total IgE (bIgE) and d-dimer (bd-dimer), and clinical parameters to omalizumab response and to relapses after drug withdrawal. METHODS: In this retrospective Italian multicentre study, clinical data were collected in 470 CSU patients, and bIgE and bd-dimer were measured in 340 and 342 patients, respectively. Disease activity was determined by Urticaria Activity Score 7 (UAS7) at week 1 and 12 after omalizumab starting. Relapses were evaluated during a 2- and 3-month interval after a first and a second course of treatment, respectively. RESULTS: bIgE correlated to a good response to omalizumab since levels were significantly higher in responders than non-responders (P = 0.0002). Conversely, bd-dimer did not correlate to response. There was no correlation between both bIgE and d-dimer and either first or second relapse. Disease duration was significantly longer in patients who experienced either first or second relapse (P < 0.0001 and P = 0.0105, respectively), while baseline UAS7 correlated only to first relapse (P = 0.0023). CONCLUSIONS: Our study confirms bIgE as a reliable biomarker predicting response to omalizumab in CSU, while it does not support the usefulness of bd-dimer unlike previous findings. CSU duration before omalizumab and baseline UAS7 may be clinical markers of relapse risk.
科研通智能强力驱动
Strongly Powered by AbleSci AI