Value Evidence, GSK, 980 Great West Road, Brentford, TW8 9GS, Middlesex, UK.
Research and Development, GSK, PTM Severo Ochoa 2 28760, Tres Cantos, Madrid, Spain.
Dig Dis Sci. 2023 Jun;68(6):2710-2730. doi: 10.1007/s10620-023-07862-z. Epub 2023 Mar 18.
We conducted a systematic literature review to understand the evidence supporting treatment decisions for cholestatic pruritus associated with primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC).
Studies that enrolled ≥ 75% participants with PBC or PSC and reported ≥ 1 endpoint(s) related to efficacy, safety, health-related quality of life (HRQoL) or other patient-reported outcomes were included. Bias was assessed using the Cochrane risk of bias tool for randomised controlled trials (RCTs) and the Quality of Cohort studies tool for non-RCTs.
Thirty-nine publications were identified, covering 42 studies and six treatment classes (including investigational and approved products): anion-exchange resins, antibiotics (rifampicin/derivatives), opiates, selective serotonin reuptake inhibitors, fibrates, ileal bile acid transporter inhibitors and other agents not categorised in these six classes. Across studies, median sample size was small (n = 18), 20 studies were over 20 years old, 25 followed patients for ≤ 6 weeks, only 25 were RCTs. Pruritus was assessed using several different tools, with inconsistencies in their application. Cholestyramine, considered first-line therapy for moderate-severe cholestatic pruritus, was assessed in six studies (two RCTs) including 56 patients with PBC and 2 with PSC, with evidence of efficacy demonstrated in only three studies, among which, two RCTs were assessed as having a high risk of bias. Findings were similar for other drug classes.
There is a lack of consistent and reproducible evidence available on efficacy, impact on HRQoL, and safety of cholestatic pruritus treatments, leaving physicians to rely on clinical experience rather than evidence-based medicine for treatment selection.
我们进行了系统文献回顾,以了解支持原发性胆汁性胆管炎(PBC)和原发性硬化性胆管炎(PSC)相关胆汁淤积性瘙痒治疗决策的证据。
纳入了≥75%的 PBC 或 PSC 参与者且报告了≥1 个与疗效、安全性、健康相关生活质量(HRQoL)或其他患者报告结局相关的终点的研究。使用 Cochrane 随机对照试验(RCT)偏倚风险工具和非 RCT 的队列研究质量工具评估偏倚。
确定了 39 篇文献,涵盖了 42 项研究和六个治疗类别(包括研究性和已批准的产品):阴离子交换树脂、抗生素(利福平/衍生物)、阿片类药物、选择性 5-羟色胺再摄取抑制剂、贝特类药物、回肠胆汁酸转运体抑制剂和其他未归类于这六类的药物。在这些研究中,中位数样本量较小(n=18),20 项研究超过 20 年,25 项研究随访时间≤6 周,仅有 25 项为 RCT。瘙痒使用了几种不同的工具进行评估,应用上存在不一致。考来烯胺被认为是中重度胆汁淤积性瘙痒的一线治疗药物,在包括 56 名 PBC 患者和 2 名 PSC 患者的 6 项研究(两项 RCT)中进行了评估,仅在三项研究中证明了疗效,其中两项 RCT 被评估为存在高偏倚风险。其他药物类别的结果相似。
在疗效、对 HRQoL 的影响和胆汁淤积性瘙痒治疗的安全性方面,缺乏一致和可重复的证据,使得医生只能依靠临床经验而不是循证医学来选择治疗方法。