社论:皮质类固醇反应性急性严重溃疡性结肠炎-在先进治疗时代重新审视维持方法

IF 6.7 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Mukesh Kumar Ranjan, Sudheer Kumar Vuyyuru
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引用次数: 0

摘要

急性严重溃疡性结肠炎(ASUC)是一种严重形式的溃疡性结肠炎(UC)爆发,需要紧急和及时的干预。大约四分之一的UC患者在其一生中经历过ASUC。ASUC的特点是频繁的血性肠蠕动和全身炎症特征。如果控制不当,可导致毒性巨结肠和结肠穿孔,通常需要紧急结肠切除术。静脉注射皮质类固醇仍然是一线治疗,尽管只有约三分之二的患者有反应[2,3]。对于无应答者,使用环孢素、英夫利昔单抗或标签外JAK抑制剂(JAKi)进行医疗救援治疗可能会诱导应答。ASUC药物治疗的主要目标是快速诱导缓解,其次是有效的维持治疗。然而,在皮质类固醇诱导成功后,指导最佳维持治疗的证据有限。Singh等人报道了一项回顾性倾向匹配分析,比较了115例接受静脉皮质类固醇治疗的成年ASUC患者将硫唑嘌呤和托法替尼作为维持治疗的有效性和安全性。作者报告,在1年内,硫唑嘌呤组的累积无事件生存率(定义为没有再住院、皮质类固醇使用、治疗升级或结肠切除术)明显低于托法替尼组(44.0%比75.0%;p = 0.01)。使用硫唑嘌呤治疗的患者有较高的再住院率(15.4%比0%,p = 0.003)和治疗升级率(13.8%比2.0%,p = 0.02), 1年症状缓解率和症状+生物标志物联合缓解率较低(40.0%比23.1%,p = 0.05; 22.0%比16.9%,p = 0.49)。虽然托法替尼组和硫唑嘌呤组的结肠切除术率相当,但结肠切除术的总体发生率仍然很低。在多变量分析中,先前暴露于免疫调节剂与维持成功率降低有关。敏感度分析排除了既往有硫唑嘌呤暴露的患者,得出了类似的结果。这些发现与随机对照ACTIVE试验一致,在该试验中,类固醇反应的患者被随机分配接受英夫利昔单抗和硫唑嘌呤或单独使用硫唑嘌呤。联合治疗组在12个月的随访中治疗失败率明显低于单药治疗组(53.3% vs. 81.5%; p = 0.03)[1]。单次ASUC发作显著增加结肠切除术的风险,随着后续发作,风险进一步上升。即使在最初接受静脉注射皮质类固醇治疗的患者中,复发和最终结肠切除术的可能性仍然很高。虽然类固醇应答者的结肠切除术风险可能低于因类固醇难治性疾病b[5]而需要医疗救助治疗的患者,但该组的复发率仍然相当高b[6]。值得注意的是,尽管Singh等人的大多数患者和ACTIVE试验的所有参与者都是azathioprine-naïve,但在硫唑嘌呤单药治疗中,有很大比例的患者在1年内复发。虽然目前的共识指南推荐硫嘌呤用于immunomodulator-naïve患者[7]的维持,但新出现的证据表明,硫嘌呤单药治疗可能不如先进的治疗有效。因此,无论初始皮质类固醇反应如何,应考虑在ASUC发作后采用先进的治疗方法进行长期维持。穆克什库马尔兰詹:写作-审查和编辑,写作-原稿。Sudheer Kumar Vuyyuru:写作-原稿,写作-审查和编辑。这篇文章链接到Singh等人的论文。要查看本文,请访问https://doi.org/10.1111/apt.70246。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Editorial: Corticosteroid Responsive Acute Severe Ulcerative Colitis—Revisiting Maintenance Approaches in the Era of Advanced Therapies

Acute severe ulcerative colitis (ASUC) is a severe form of ulcerative colitis (UC) flare that requires urgent and timely intervention. Approximately one-fourth of patients with UC experience ASUC during their lifetime [1]. ASUC is characterised by frequent bloody bowel movements and systemic inflammatory features. If not adequately controlled, it can lead to toxic megacolon and colonic perforation, often necessitating emergency colectomy. Intravenous corticosteroids remain the first-line treatment, although only about two-thirds of patients respond [2, 3]. For non-responders, medical rescue therapy with cyclosporin, infliximab, or off-label JAK inhibitors (JAKi) may induce response. The primary goal of medical therapy in ASUC is rapid induction of remission, followed by effective maintenance therapy. However, there is limited evidence to guide optimal maintenance therapy following successful induction with corticosteroids.

Singh et al. [4] reported a retrospective propensity-matched analysis comparing the effectiveness and safety of azathioprine and tofacitinib as maintenance therapy in 115 adult patients with ASUC who responded to intravenous corticosteroids. The authors reported a significantly lower cumulative probability of event-free survival (defined as absence of rehospitalization, corticosteroid use, therapy escalation, or colectomy) at 1 year in the azathioprine than in the tofacitinib group (44.0% vs. 75.0%; p = 0.01). Patients managed with azathioprine had higher rates of re-hospitalisation (15.4% vs. 0%; p = 0.003) and treatment escalation (13.8% vs. 2.0%; p = 0.02), and lower rates of symptomatic remission and combined symptomatic plus biomarker remission at 1 year (40.0% vs. 23.1%; p = 0.05; 22.0% vs. 16.9%; p = 0.49, respectively). Although colectomy rates were comparable between the tofacitinib and azathioprine groups, the overall incidence of colectomy remained very low. On multivariate analysis, prior exposure to immunomodulators was associated with reduced maintenance success. A sensitivity analysis excluding patients with prior azathioprine exposure yielded similar results. These findings are consistent with the randomised controlled ACTIVE trial, in which steroid-responsive patients were randomised to receive infliximab and azathioprine or azathioprine alone. The combination therapy group had significantly lower rates of treatment failure over 12 months' follow-up compared to the azathioprine monotherapy group (53.3% vs. 81.5%; p = 0.03) [1].

A single episode of ASUC substantially increases the risk of colectomy, with the risk rising further with subsequent episodes [1]. Even in patients who initially respond to intravenous corticosteroids, the likelihood of relapse and eventual colectomy remains high. While steroid responders may have a lower colectomy risk than those who required medical rescue therapy due to steroid-refractory disease [5], the relapse rate in this group is still considerably high [6]. Notably, although most patients of Singh et al. and all participants in the ACTIVE trial were azathioprine-naïve, a significant proportion on azathioprine monotherapy experienced relapse within 1 year. Although current consensus guidelines recommend thiopurines for maintenance in immunomodulator-naïve patients [7], emerging evidence indicates that azathioprine monotherapy may be less effective than advanced therapies. Therefore, advanced therapies should be considered for long-term maintenance after an ASUC episode, regardless of the initial corticosteroid response.

Mukesh Kumar Ranjan: writing – review and editing, writing – original draft. Sudheer Kumar Vuyyuru: writing – original draft, writing – review and editing.

This article is linked to Singh et al. paper. To view this article, visit https://doi.org/10.1111/apt.70246.

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来源期刊
CiteScore
15.60
自引率
7.90%
发文量
527
审稿时长
3-6 weeks
期刊介绍: Alimentary Pharmacology & Therapeutics is a global pharmacology journal focused on the impact of drugs on the human gastrointestinal and hepato-biliary systems. It covers a diverse range of topics, often with immediate clinical relevance to its readership.
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