Lehmann Sylvia, Pfannenstiel Claus, Friedrichs Frank, Kröger Kristina, Wagner Norbert, Tenbrock Klaus
Department of Paediatric Pulmonology, University Hospital RWTH Aachen, Germany
Practice for Paediatric Pulmonology, Aachen, Germany.
Ther Adv Respir Dis. 2014 Oct;8(5):141-9. doi: 10.1177/1753465814547517. Epub 2014 Aug 21.
Allergic bronchopulmonary aspergillosis (ABPA) is a severe complication in patients with cystic fibrosis (CF), resulting in deterioration of lung function and impairment of overall prognosis. Standard therapy consists of high dosage, long-term corticosteroid treatment. This carries the risk of serious side effects such as immune suppression, diabetes and osteoporosis. Antifungal drugs such as itraconazole may cause interactions with other drugs and drug levels need to be monitored. Omalizumab treatment has been tried in several case studies.
This was a retrospective study of six patients (four female, two male, age 4-33 years old) with CF and ABPA treated with omalizumab within an observation period of 7.5 years.
All patients showed clinical and laboratory stability or even an improvement within the treatment and post-treatment observation period, although omalizumab therapy was less effective in patients with progressed lung disease and long-term ABPA. Side effects of systemic steroids were reduced.
Omalizumab has the potential to be an additional and solitary treatment option in patients with CF and ABPA. Early onset treatment may be beneficial and patients with early stage of lung disease seem to benefit more.
变应性支气管肺曲霉病(ABPA)是囊性纤维化(CF)患者的一种严重并发症,会导致肺功能恶化及总体预后受损。标准治疗包括高剂量、长期的皮质类固醇治疗。这存在免疫抑制、糖尿病和骨质疏松等严重副作用的风险。伊曲康唑等抗真菌药物可能会与其他药物发生相互作用,需要监测药物水平。在一些病例研究中尝试过奥马珠单抗治疗。
这是一项对6例CF合并ABPA患者(4例女性,2例男性,年龄4至33岁)进行的回顾性研究,观察期为7.5年,这些患者接受了奥马珠单抗治疗。
所有患者在治疗及治疗后观察期内均表现出临床和实验室指标稳定甚至有所改善,尽管奥马珠单抗治疗对肺部疾病进展和长期ABPA患者的效果较差。全身用类固醇的副作用减少。
奥马珠单抗有可能成为CF合并ABPA患者的一种额外且单独的治疗选择。早期开始治疗可能有益,且肺部疾病早期患者似乎获益更多。