Division of Gastroenterology and Hepatology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Robarts Clinical Trials, Western University, London, Ontario, Canada.
Aliment Pharmacol Ther. 2019 Feb;49(4):364-374. doi: 10.1111/apt.15090. Epub 2018 Dec 19.
Aminosalicylates are the most frequently prescribed treatment for ulcerative colitis (UC). In the absence of empirical evidence, clinicians are uncertain whether to continue aminosalicylates in patients with UC after escalating therapy.
To quantify concomitant aminosalicylate use in UC randomised clinical trials (RCTs), identify factors associated with their use, and estimate treatment costs of concomitant aminosalicylate therapy.
MEDLINE, Embase, and CENTRAL were searched from inception to 1 March 2017 for placebo-controlled RCTs of immunosuppressants, biologics, or oral small molecules in adults with UC. The proportion of patients prescribed concomitant aminosalicylates at trial entry was pooled using a random-effects model. Meta-regression was performed to assess trial-level factors associated with aminosalicylate use. Treatment costs were estimated using 2018 formulary data from five Canadian provinces.
Thirty-two trials were included (23 induction only, nine induction, and maintenance trials). The pooled proportion of patients co-prescribed aminosalicylates was 80.7% (95% CI 75.5%-85.1%), with considerable observed heterogeneity (I = 95%). In univariable meta-regression, aminosalicylate use was not associated with trial design, setting, year of publication, disease severity, disease duration, or drug class. The estimated direct annual treatment cost of concomitant aminosalicylates is ~$20 million for the Canadian UC population, assuming conservative estimates of UC prevalence, aminosalicylate use and dose, and the lowest cost formulation.
Approximately 80% of UC patients entering clinical trials of immunosuppressants, biologics, or oral small molecules continue to use aminosalicylates. An RCT is needed to inform the benefits and harms of continuing vs stopping aminosalicylates in patients escalating therapy.
氨基水杨酸盐是溃疡性结肠炎(UC)最常开的治疗药物。在缺乏经验证据的情况下,临床医生不确定在升级治疗后是否应继续为 UC 患者开氨基水杨酸盐。
定量评估 UC 随机临床试验(RCT)中同时使用氨基水杨酸盐的情况,确定与使用相关的因素,并估算同时使用氨基水杨酸盐治疗的治疗费用。
从建库至 2017 年 3 月 1 日,通过 MEDLINE、Embase 和 CENTRAL 检索了氨基水杨酸酯、免疫抑制剂、生物制剂或口服小分子药物治疗成人 UC 的安慰剂对照 RCT。采用随机效应模型汇总了试验开始时同时使用氨基水杨酸盐的患者比例。进行荟萃回归分析,以评估与氨基水杨酸盐使用相关的试验水平因素。使用来自加拿大五个省份的 2018 年定价数据来估算治疗费用。
纳入了 32 项试验(23 项仅诱导治疗,9 项诱导和维持治疗)。同时使用氨基水杨酸盐的患者比例为 80.7%(95%CI 75.5%-85.1%),观察到显著的异质性(I²=95%)。在单变量荟萃回归中,氨基水杨酸盐的使用与试验设计、试验地点、发表年份、疾病严重程度、疾病持续时间或药物类别无关。假设对 UC 患病率、氨基水杨酸盐使用和剂量以及最低成本配方进行保守估计,加拿大 UC 人群同时使用氨基水杨酸盐的直接年度治疗费用估计约为 2000 万美元。
大约 80%的 UC 患者在接受免疫抑制剂、生物制剂或口服小分子药物临床试验时继续使用氨基水杨酸盐。需要进行 RCT 来明确在升级治疗的患者中继续或停止使用氨基水杨酸盐的获益和危害。