Papaioannou Andriana I, Kallieri Maria, Zervas Eleftherios, Fouka Evangelia, Porpodis Konstantinos, Hadji Mitrova Marija, Tzortzaki Eleni, Makris Michael, Ntakoula Maria, Lyberopoulos Panagiotis, Dimakou Katerina, Koukidou Sofia, Ampelioti Sevasti, Papaporfyriou Anastasia, Katsoulis Konstantinos, Kipourou Maria, Rovina Nikoletta, Antoniou Katerina, Vittorakis Stylianos, Bakakos Petros, Steiropoulos Paschalis, Markopoulou Katerina, Avarlis Panteleimon, Papanikolaou Ιlias C, Markatos Miltiadis, Gaki Eleni, Samitas Konstantinos, Glynos Konstantinos, Papiris Spyros A, Papakosta Despoina, Tzanakis Nikolaos, Gaga Mina, Kostikas Konstantinos, Loukides Stelios
From the 1st Respiratory Department, Sotiria Chest Hospital, National and Kapodistrian University of Athens Medical School, Athens, Greece.
2nd Respiratory Department, Attikon University Hospital, National and Kapodistrian University of Athens Medical School, Athens, Greece.
Allergy Asthma Proc. 2025 Jan 1;46(1):45-51. doi: 10.2500/aap.2025.46.240084.
Remission of asthma can occur as part of the natural history of the disease; however, the use of biologics can result in disease remission in some patients. In this post hoc analysis of the RELIght study, we aimed to evaluate clinical remission in real life among patients treated with mepolizumab, to detect possible differences between "remitters" and "nonremitters," and to evaluate possible predictors of remission. Clinical remission was defined as the absence of asthma exacerbations, discontinuation of oral corticosteroids (OCS), achievement of asthma control (Asthma Control Test [ACT] ≥ 20), and stable or improved lung function. A total of 146 patients were evaluated; remission was achieved in 40 (27.4%) and 29 (22%) after 12 and 24 months, respectively. At 12 months, the patients in remission had a better baseline ACT score (17.0 [14.0-19.0] versus 15.0 [12.0-17.0]; p = 0.027), were more rarely using OCS (35% versus 62.2%; p = 0.004), and required a lower baseline dose of OCS (5.0 mg/day [5.0-10.0 mg/day] versus 10.0 mg/day [5.0-15.0 mg/day]; p = 0.042) at baseline, whereas, at 24 months, they less frequently carried a baseline diagnosis of gastroesophageal reflux disease (GERD) (10.3% versus 32%; p = 0.031) and used lower doses of OCS at baseline (5.0 [1.0-5.0] versus 10.0 [5.0-15.0]; p = ≤0.001) versus nonremitters; 52.5% of patients had sustained remission, whereas 42.5% experienced relapse. These patients more frequently had GERD versus patients with sustained remission (52.9% versus 4.8%; p = 0.002). Finally, regression analysis has shown that GERD was the only predictor of relapse. Remitters had better asthma control and needed lower doses or no maintenance OCS at baseline, whereas GERD seems to be an important factor that affects remission and relapse.Clinical trial NCT04084613,
哮喘缓解可能是疾病自然史的一部分;然而,使用生物制剂可使部分患者实现疾病缓解。在这项针对RELIght研究的事后分析中,我们旨在评估接受美泊利珠单抗治疗的患者在现实生活中的临床缓解情况,检测“缓解者”与“未缓解者”之间可能存在的差异,并评估缓解的可能预测因素。临床缓解定义为无哮喘急性发作、停用口服糖皮质激素(OCS)、实现哮喘控制(哮喘控制测试[ACT]≥20)以及肺功能稳定或改善。总共评估了146例患者;分别在12个月和24个月后,40例(27.4%)和29例(22%)实现了缓解。在12个月时,缓解的患者基线ACT评分更高(17.0[14.0 - 19.0] vs 15.0[12.0 - 17.0];p = 0.027),使用OCS的频率更低(35% vs 62.2%;p = 0.004),且基线时所需的OCS剂量更低(5.0毫克/天[5.0 - 10.0毫克/天] vs 10.0毫克/天[5.0 - 15.0毫克/天];p = 0.042),而在24个月时,他们基线时患有胃食管反流病(GERD)的诊断频率更低(10.3% vs 32%;p = 0.031),且基线时使用的OCS剂量更低(5.0[1.0 - 5.0] vs 10.0[5.0 - 15.0];p≤0.001),与未缓解者相比;52.5%的患者实现了持续缓解,而42.5%的患者经历了复发。与持续缓解的患者相比,这些患者患GERD的频率更高(52.9% vs 4.8%;p = 0.002)。最后,回归分析表明GERD是复发的唯一预测因素。缓解者哮喘控制更好,基线时需要更低剂量或无需维持使用OCS,而GERD似乎是影响缓解和复发的重要因素。临床试验NCT04084613,<网址链接 xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="http://www.clinical trials.gov">www.clinical trials.gov</网址链接> 。