Yamamoto Takayuki, Umegae Satoru, Matsumoto Koichi
World J Gastroenterol. 2006 Jan 28;12(4):520-5. doi: 10.3748/wjg.v12.i4.520.
Active ulcerative colitis (UC) is frequently associated with infiltration of a large number of leukocytes into the bowel mucosa. Therefore, removal of activated circulating leukocytes by apheresis has the potential for improving UC. In Japan, since April 2000, leukocytapheresis using Adacolumn has been approved as the treatment for active UC by the Ministry of Health and Welfare. The Adacolumn is an extracorporeal leukocyte apheresis device filled with cellulose acetate beads, and selectively adsorbs granulocytes and monocytes/macrophages. To assess the safety and clinical efficacy of granulocyte and monocyte adsorptive apheresis (GMCAP) for UC, we reviewed 10 open trials of the use of GMCAP to treat UC. One apheresis session (session time, 60 min) per week for five consecutive weeks (a total of five apheresis sessions) has been a standard protocol. Several studies used modified protocols with two sessions per week, with 90-min session, or with a total of 10 apheresis sessions. Typical adverse reactions were dizziness, nausea, headache, flushing, and fever. No serious adverse effects were reported during and after GMCAP therapy, and almost all the patients could complete the treatment course. GMCAP is safe and well-tolerated. In the majority of patients, GMCAP therapy achieved clinical remission or improvement. GMCAP is a useful alternative therapy for patients with steroid-refractory or -dependent UC. GMCAP should have the potential to allow tapering the dose of steroids, and is useful for shortening the time to remission and avoiding re-administration of steroids at the time of relapse. Furthermore, GMCAP may have efficacy as the first-line therapy for steroid-naive patients or patients who have the first attack of UC. However, most of the previous studies were uncontrolled trials. To assess a definite efficacy of GMCAP, randomized, double-blind, sham-controlled trials are necessary. A serious problem with GMCAP is cost; a single session costs 145 000 ($1 300). However, if this treatment prevents hospital admission, re-administration of steroids and surgery, and improves a quality of life of the patients, GMCAP may prove to be cost-effective.
活动性溃疡性结肠炎(UC)常伴有大量白细胞浸润至肠黏膜。因此,通过血液成分单采去除活化的循环白细胞有可能改善UC。在日本,自2000年4月起,使用阿达柱(Adacolumn)进行白细胞单采已被厚生省批准为活动性UC的治疗方法。阿达柱是一种填充有醋酸纤维素珠的体外白细胞单采装置,可选择性吸附粒细胞和单核细胞/巨噬细胞。为评估粒细胞和单核细胞吸附性单采(GMCAP)治疗UC的安全性和临床疗效,我们回顾了10项使用GMCAP治疗UC的开放性试验。标准方案为连续五周每周进行一次单采治疗(每次治疗时间60分钟,共五次单采治疗)。几项研究采用了修改后的方案,即每周进行两次治疗、每次治疗90分钟或总共进行10次单采治疗。典型的不良反应有头晕、恶心、头痛、潮红和发热。在GMCAP治疗期间及之后未报告严重不良反应,几乎所有患者都能完成治疗疗程。GMCAP安全且耐受性良好。在大多数患者中,GMCAP治疗实现了临床缓解或病情改善。GMCAP是对类固醇难治性或依赖性UC患者有用的替代疗法。GMCAP应有可能减少类固醇剂量,有助于缩短缓解时间并避免复发时再次使用类固醇。此外,GMCAP可能对初治患者或首次发作UC的患者作为一线治疗有效。然而,之前的大多数研究都是非对照试验。为评估GMCAP的确切疗效,有必要进行随机、双盲、假对照试验。GMCAP的一个严重问题是成本;单次治疗费用为145000日元(1300美元)。然而,如果这种治疗能防止患者住院、再次使用类固醇和手术,并改善患者生活质量,GMCAP可能被证明具有成本效益。