Freund Ophir, Meoded Omer, Arnaout Tala, Friedman Regev Inbal, Kupershmidt Aviv, Enghelberg Sharon, Cohn-Schwartz Doron, Levy Liran, Bar-Shai Amir
The Institute of Pulmonary Medicine, Tel-Aviv Sourasky Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
The Sheba Lung Transplant Program and Institute of Pulmonary Medicine, Sheba Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Int J Chron Obstruct Pulmon Dis. 2025 Aug 6;20:2753-2760. doi: 10.2147/COPD.S525781. eCollection 2025.
Dupilumab was recently shown to be effective in patients with chronic obstructive pulmonary disease (COPD) and type 2 inflammation, while real-world data are missing. We aimed to evaluate the experience of COPD patients treated with Dupilumab.
Consecutive patients with COPD treated with Dupilumab were approached and completed a structured interview. Before treatment, all patients had blood eosinophil count ≥300 cells/μL and prior-year exacerbations despite triple inhaler therapy.
Twenty-three subjects were included, with median (IQR) treatment of 320 (280-355) days, median age of 75 years, and 52% female. A decrease in mean annualize exacerbation rate was observed from 3.47 at baseline to 1.55 after treatment (55% reduction). Number of severe exacerbations decreased as well (median 1 vs 0 over the same time frame). There was a decrease in the median COPD assessment test scores (median of 18 vs 15), although FEV1 did not change. One patient had skin-related side effect. Sixty-one percent were content with the treatment, and 74% would recommend it to others with COPD. During interview, patients reported on their need and openness to new and safe treatment options. Using the Global Evaluation of Treatment Effectiveness (GETE) tool, 30% reported on marked improvements following dupilumab. Treatment limitations were costs (48%) and repeated injections (21%).
In this case-series, dupilumab was shown to be well tolerated and was associated with lower rates of exacerbations and improved symptoms. These outcomes were supported by patient reported outcome measurements.
度普利尤单抗最近被证明对慢性阻塞性肺疾病(COPD)合并2型炎症患者有效,但缺乏真实世界的数据。我们旨在评估接受度普利尤单抗治疗的COPD患者的经验。
对连续接受度普利尤单抗治疗的COPD患者进行了接触并完成了结构化访谈。治疗前,所有患者尽管接受了三联吸入器治疗,但血嗜酸性粒细胞计数≥300个细胞/μL且有上一年的急性加重发作。
纳入23名受试者,中位(四分位间距)治疗时间为320(280 - 355)天,中位年龄75岁,女性占52%。观察到平均年化急性加重率从基线时的3.47降至治疗后的1.55(降低55%)。严重急性加重发作的次数也减少了(同一时间段内中位数从1次降至0次)。COPD评估测试评分中位数有所下降(中位数从18降至15),尽管第1秒用力呼气容积(FEV1)没有变化。1例患者出现与皮肤相关的副作用。61%的患者对治疗满意,74%的患者会向其他COPD患者推荐。在访谈中,患者报告了他们对新的安全治疗选择的需求和接受程度。使用全球治疗效果评估(GETE)工具,30%的患者报告度普利尤单抗治疗后有显著改善。治疗的局限性在于费用(48%)和重复注射(21%)。
在这个病例系列中,度普利尤单抗显示出耐受性良好,且与较低的急性加重率和症状改善相关。这些结果得到了患者报告的结局指标的支持。