Thoraxklinik am Universitätsklinikum Heidelberg, Heidelberg, Germany. Felix.Herth @ thoraxklinik-heidelberg.de
Respiration. 2011;82(1):36-45. doi: 10.1159/000322649. Epub 2011 Jan 11.
This report summarizes initial tests of an emphysematous lung synthetic polymer sealant (ELS) designed to reduce lung volume in patients with advanced emphysema.
The primary study objective was to define a therapeutic strategy to optimize treatment safety and effectiveness.
ELS therapy was administered bronchoscopically to 25 patients with heterogeneous emphysema in an open-label, noncontrolled study at 6 centers in Germany. Treatment was performed initially at 2-4 subsegments. After 12 weeks, patients were eligible for repeat therapy to a total of 6 sites. Safety and efficacy were assessed after 6 months. Responses were evaluated in terms of changes from baseline in lung physiology, functional capacity, and health-related quality of life. Follow-up is available for 21 of 25 patients.
Treatment was well tolerated. There were no treatment-related deaths (i.e., within 90 days of treatment), and an acceptable short- and long-term safety profile. Physiological and clinical benefits were observed at 24 weeks. Efficacy responses were better among Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage III patients [n = 14; change in residual volume/total lung capacity (ΔRV/TLC) = -7.4 ± 10.3%; Δ forced expiratory volume in 1 s (ΔFEV(1)) = +15.9 ± 22.6%; change in forced vital capacity (ΔFVC) = +24.1 ± 22.7%; change in carbon monoxide lung diffusion capacity (ΔDLCO) = +19.3 ± 34.8%; change in 6-min walk test (Δ6MWD) = +28.7 ± 59.6 m; change in Medical Research Council Dyspnea (ΔMRCD) score = -1.0 ± 1.04 units; change in St. George's Respiratory Questionnaire (ΔSGRQ) score = -9.9 ± 15.3 units] than for GOLD stage IV patients (n = 7; ΔRV/TLC = -0.5 ± 6.4%; ΔFEV(1) = +2.3 ± 12.3%; ΔFVC = +2.6 ± 21.1%; ΔDLCO = -2.8 ± 17.2%; Δ6MWD = +28.3 ± 58.4 m; ΔMRCD = 0.3 ± 0.81 units; ΔSGRQ = -6.7 ± 7.0 units).
ELS therapy shows promise for treating patients with advanced heterogeneous emphysema. Additional studies to assess responses in a larger cohort with a longer follow-up are warranted.
本报告总结了一种用于减少晚期肺气肿患者肺容积的肺气肿合成聚合物密封剂(ELS)的初步测试结果。
主要研究目的是确定一种治疗策略,以优化治疗的安全性和有效性。
在德国的 6 个中心进行了一项开放标签、非对照研究,25 例异质性肺气肿患者接受了 ELS 治疗。最初在 2-4 个亚段进行治疗。12 周后,患者有资格接受总共 6 个部位的重复治疗。6 个月后评估安全性和疗效。根据肺生理、功能能力和健康相关生活质量的基线变化来评估反应。25 例患者中有 21 例可获得随访。
治疗耐受性良好。无治疗相关死亡(即治疗后 90 天内),且短期和长期安全性良好。24 周时观察到生理和临床获益。全球慢性阻塞性肺疾病倡议(GOLD)III 期患者(n=14)的疗效反应更好[残气量/肺总量(ΔRV/TLC)变化=-7.4±10.3%;第 1 秒用力呼气量(ΔFEV1)变化=+15.9±22.6%;用力肺活量(ΔFVC)变化=+24.1±22.7%;一氧化碳肺扩散量(ΔDLCO)变化=+19.3±34.8%;6 分钟步行试验(Δ6MWD)变化=+28.7±59.6 m;改良医学研究理事会呼吸困难量表(ΔMRCD)评分变化=-1.0±1.04 单位;圣乔治呼吸问卷(ΔSGRQ)评分变化=-9.9±15.3 单位],而 GOLD IV 期患者(n=7)的疗效反应较差[ΔRV/TLC=0.5±6.4%;ΔFEV1=+2.3±12.3%;ΔFVC=+2.6±21.1%;ΔDLCO=-2.8±17.2%;Δ6MWD=+28.3±58.4 m;ΔMRCD=0.3±0.81 单位;ΔSGRQ=-6.7±7.0 单位]。
ELS 治疗为治疗晚期异质性肺气肿患者提供了希望。需要进一步的研究来评估更大队列和更长随访时间的反应。