van der Vaart Hester, Koëter Gerard H, Postma Dirkje S, Kauffman Henk F, ten Hacken Nick H T
Department of Pulmonology, University Medical Center Groningen, P.O. Box 30.001, NL-9700 RB, Groningen, the Netherlands.
Am J Respir Crit Care Med. 2005 Aug 15;172(4):465-9. doi: 10.1164/rccm.200501-147OC. Epub 2005 Jun 3.
Tumor necrosis factor-alpha is believed to be important in the induction and maintenance of airway inflammation in chronic obstructive pulmonary disease.
We aimed to evaluate the effect of the anti-tumor necrosis factor-alpha drug infliximab in patients with chronic obstructive pulmonary disease, with percentage of sputum neutrophils as the primary endpoint.
We performed an exploratory single-center, double-blind, placebo-controlled, randomized, phase 2 trial in which 22 current smokers with mild-to-moderate chronic obstructive pulmonary disease participated. Fourteen patients received three infusions of infliximab (5 mg/kg) at Weeks 0, 2, and 6, and eight patients received placebo infusions. Sputum samples, respiratory symptoms, quality of life, exhaled nitric oxide, lung function parameters, bronchial hyperresponsiveness, resting energy expenditure, and side effects were evaluated.
This study did not show a positive short-term effect of infliximab on airway inflammation, lung function, resting energy expenditure, or quality of life. Exhaled nitric oxide increased significantly at Day 2, Week 6, and Week 8 in patients receiving infliximab compared with those receiving placebo. Eight patients in the infliximab group (vs. none in the placebo group) reported increased coughing, but no serious adverse events or increase in respiratory infections were reported during 9 weeks of follow-up.
In this short-term study, no clinically beneficial effects of infliximab were observed, and there were no significant safety issues. Definite conclusions concerning the effectiveness of infliximab treatment in chronic obstructive pulmonary disease await additional studies, including those with a larger number of patients with more advanced disease.
肿瘤坏死因子-α被认为在慢性阻塞性肺疾病气道炎症的诱导和维持中起重要作用。
我们旨在评估抗肿瘤坏死因子-α药物英夫利昔单抗对慢性阻塞性肺疾病患者的疗效,以痰液中性粒细胞百分比作为主要终点。
我们进行了一项探索性单中心、双盲、安慰剂对照、随机2期试验,22名患有轻至中度慢性阻塞性肺疾病的现吸烟者参与其中。14名患者在第0、2和6周接受三次英夫利昔单抗(5mg/kg)输注,8名患者接受安慰剂输注。对痰液样本、呼吸道症状、生活质量、呼出一氧化氮、肺功能参数、支气管高反应性、静息能量消耗和副作用进行了评估。
本研究未显示英夫利昔单抗对气道炎症、肺功能、静息能量消耗或生活质量有短期积极影响。与接受安慰剂的患者相比,接受英夫利昔单抗的患者在第2天、第6周和第8周呼出一氧化氮显著增加。英夫利昔单抗组有8名患者(安慰剂组无)报告咳嗽增加,但在9周的随访期间未报告严重不良事件或呼吸道感染增加。
在这项短期研究中,未观察到英夫利昔单抗有临床有益效果,也没有明显的安全问题。关于英夫利昔单抗治疗慢性阻塞性肺疾病有效性的确切结论有待进一步研究,包括对更多病情更严重患者的研究。