Division of Gastroenterology and Hepatology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Robarts Clinical Trials, Western University, London, ON, Canada.
Aliment Pharmacol Ther. 2018 Jul;48(2):114-126. doi: 10.1111/apt.14821. Epub 2018 May 30.
Aminosalicylates are the most frequently prescribed drugs for patients with Crohn's disease (CD), yet evidence to support their efficacy as induction or maintenance therapy is controversial.
To quantify aminosalicylate use in CD clinical trials, identify factors associated with use and estimate direct annual treatment costs of therapy.
MEDLINE, Embase and CENTRAL were searched to April 2017 for placebo-controlled trials in adults with CD treated with corticosteroids, immunosuppressants or biologics. The proportion of patients co-prescribed aminosalicylates in placebo arms was pooled using a random-effects model. Meta-regression was used to identify factors associated with aminosalicylate use. Annual treatment costs were estimated using the 2016 Ontario Drug Benefit Program.
Forty-two induction and 10 maintenance trials were included. The pooled proportion of patients co-prescribed aminosalicylates was 44% [95% CI: 39%-49%] in induction trials and 49% [95% CI: 35%-64%] in maintenance trials. There was substantial to considerable heterogeneity (I = 86.0%, 91.8% for induction and maintenance trials, respectively). In multivariable meta-regression, aminosalicylate use has decreased over time in induction trials (OR 0.50 [95% CI: 0.34-0.74] per 10-year increment). While a decline has been seen over time, 35% of CD patients were still using aminosalicylates in contemporary trials from the last 5 years. The estimated annual cost for the lowest price mesalazine (mesalamine) formulation is approximately $32 million for the Canadian CD population.
Over one-third of CD patients entering clinical trials are still co-prescribed aminosalicylates. A definitive trial is needed to inform the conventional practice of using aminosalicylates as CD maintenance therapy.
氨基水杨酸盐是治疗克罗恩病(CD)患者最常用的药物,但支持其作为诱导或维持治疗疗效的证据存在争议。
量化 CD 临床试验中氨基水杨酸盐的使用情况,确定与使用相关的因素,并估计治疗的直接年度治疗费用。
检索 MEDLINE、Embase 和 CENTRAL,以获取 2017 年 4 月前发表的治疗接受皮质类固醇、免疫抑制剂或生物制剂治疗的成人 CD 的安慰剂对照试验。使用随机效应模型汇总安慰剂组中同时使用氨基水杨酸盐的患者比例。采用元回归分析确定与氨基水杨酸盐使用相关的因素。使用 2016 年安大略省药物福利计划估计年度治疗费用。
纳入 42 项诱导治疗试验和 10 项维持治疗试验。诱导治疗试验中同时使用氨基水杨酸盐的患者比例为 44%[95%CI:39%-49%],维持治疗试验中为 49%[95%CI:35%-64%]。存在很大到相当大的异质性(I = 86.0%,分别为诱导和维持治疗试验)。在多变量元回归分析中,诱导治疗试验中氨基水杨酸盐的使用随着时间的推移而减少(每增加 10 年 OR 0.50[95%CI:0.34-0.74])。虽然随着时间的推移有所下降,但在最近 5 年的当代试验中,仍有 35%的 CD 患者在使用氨基水杨酸盐。加拿大 CD 人群中,最低价格美沙拉嗪(柳氮磺胺吡啶)制剂的年估计费用约为 3200 万美元。
超过三分之一进入临床试验的 CD 患者仍同时使用氨基水杨酸盐。需要进行一项明确的试验,以告知使用氨基水杨酸盐作为 CD 维持治疗的常规实践。