Real-life effectiveness and safety of tofacitinib treatment in patients with ulcerative colitis: a KASID multicenter cohort study.

IF 4.2 3区 医学
Therapeutic Advances in Gastroenterology Pub Date : 2023-03-18 eCollection Date: 2023-01-01 DOI:10.1177/17562848231154103
Seung Hwan Shin, Kyunghwan Oh, Sung Noh Hong, Jungbok Lee, Shin Ju Oh, Eun Soo Kim, Soo-Young Na, Sang-Bum Kang, Seong-Joon Koh, Ki Bae Bang, Sung-Ae Jung, Sung Hoon Jung, Kyeong Ok Kim, Sang Hyoung Park, Suk-Kyun Yang, Chang Hwan Choi, Byong Duk Ye
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引用次数: 0

Abstract

Background: Tofacitinib is a small molecule that inhibits Janus kinase and has been reported to be effective in Western patients with ulcerative colitis (UC). However, the real-life data on tofacitinib in Asian UC patients are limited.

Objective: To investigate the real-life effectiveness and safety of tofacitinib induction and maintenance treatment in Korean patients with UC.

Design: This was a retrospective study on patients with UC who received tofacitinib treatment at 12 hospitals in Korea between January 2018 and November 2020.

Methods: Clinical remission at week 52, defined as a partial Mayo score of ⩽2 with a combined rectal bleeding subscore and stool frequency subscore of ⩽1, was used as the primary outcome. Adverse events (AEs), including herpes zoster and deep vein thrombosis, were also evaluated.

Results: A total of 148 patients with UC were started on tofacitinib. Clinical remission rates of 60.6%, 54.9%, and 52.8% were reported at weeks 16, 24, and 52, respectively. Clinical response rates of 71.8%, 67.6%, and 59.9% were reported at weeks 16, 24, and 52, respectively. Endoscopic remission rates at weeks 16 and 52 were 52.4% and 30.8% based on the Mayo endoscopic subscore and 20.7% and 15.2% based on the UC endoscopic index of severity (UCEIS), respectively. A higher UCEIS at baseline was negatively associated with clinical response [adjusted odds ratio (aOR): 0.774, p = 0.029] and corticosteroid-free clinical response (aOR: 0.782, p = 0.035) at week 52. AEs occurred in 19 patients (12.8%) and serious AEs in 12 patients (8.1%). Herpes zoster occurred in four patients (2.7%). One patient (0.7%) suffered from deep vein thrombosis.

Conclusions: Tofacitinib was an effective induction and maintenance treatment with an acceptable safety profile in Korean patients with UC.

Plain language summary: Real-life effectiveness and safety of tofacitinib treatment in Korean patients with ulcerative colitis Ulcerative colitis (UC) is an idiopathic, chronic inflammatory disorder of the colonic mucosa that usually presents with bloody diarrhea and abdominal pain. Tofacitinib is a small molecule that inhibits Janus kinase and has been reported to be effective in Western patients with UC. However, real-life data on the effectiveness of tofacitinib in Asian patients with UC are limited. To investigate the real-life effectiveness and safety of tofacitinib treatment in Korean patients with UC, we retrospectively analyzed the data of 148 patients with UC who received tofacitinib treatment at 12 hospitals in Korea between January 2018 and November 2020. Clinical remission (i.e. complete improvement of symptoms) was achieved in 60.6% and 52.8% of patients at weeks 16 and 52, respectively. Endoscopic remission was achieved in 52.4% and 30.8% of patients at weeks 16 and 52, respectively. A higher baseline score of the UC endoscopic index of severity, which is one of the endoscopic indices that evaluate the severity of inflammation of the colon, was negatively associated with clinical response (i.e. partial improvement of symptoms). Adverse events (AEs) including herpes zoster and deep vein thrombosis occurred in 19 patients (12.8%) and serious AEs occurred in 12 patients (8.1%). Our real-life study shows that tofacitinib is a clinically effective treatment for Korean patients with UC, and the incidence of AEs was also similar to those observed in other real-world studies.

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托法替尼治疗溃疡性结肠炎患者的实际有效性和安全性:KASID 多中心队列研究。
背景:托法替尼是一种抑制Janus激酶的小分子药物,据报道对西方溃疡性结肠炎(UC)患者有效。然而,有关托法替尼在亚洲溃疡性结肠炎患者中的实际应用数据却很有限:调查韩国 UC 患者接受托法替尼诱导和维持治疗的实际有效性和安全性:这是一项回顾性研究,研究对象为2018年1月至2020年11月期间在韩国12家医院接受过托法替尼治疗的UC患者:第52周的临床缓解定义为部分梅奥评分⩽2,直肠出血子评分和大便次数子评分合计⩽1,作为主要结果。此外,还对包括带状疱疹和深静脉血栓形成在内的不良事件(AEs)进行了评估:共有148名UC患者开始服用托法替尼。第16、24和52周的临床缓解率分别为60.6%、54.9%和52.8%。第16、24和52周的临床应答率分别为71.8%、67.6%和59.9%。根据梅奥内镜子评分,第16周和第52周的内镜缓解率分别为52.4%和30.8%,根据UC内镜严重程度指数(UCEIS),内镜缓解率分别为20.7%和15.2%。基线时 UCEIS 较高与第 52 周时的临床应答[调整后比值比 (aOR):0.774,p = 0.029]和无皮质类固醇临床应答(aOR:0.782,p = 0.035)呈负相关。19名患者(12.8%)出现了不良反应,12名患者(8.1%)出现了严重不良反应。四名患者(2.7%)出现带状疱疹。一名患者(0.7%)出现深静脉血栓:在韩国UC患者中,托法替尼是一种有效的诱导和维持治疗药物,其安全性可接受:托法替尼治疗韩国溃疡性结肠炎患者的实际有效性和安全性 溃疡性结肠炎(UC)是一种特发性结肠粘膜慢性炎症性疾病,通常表现为血性腹泻和腹痛。托法替尼是一种抑制 Janus 激酶的小分子药物,据报道对西方 UC 患者有效。然而,有关托法替尼对亚洲 UC 患者疗效的实际数据却很有限。为了研究托法替尼治疗韩国 UC 患者的实际有效性和安全性,我们回顾性分析了 2018 年 1 月至 2020 年 11 月期间在韩国 12 家医院接受托法替尼治疗的 148 例 UC 患者的数据。在第16周和第52周,分别有60.6%和52.8%的患者实现了临床缓解(即症状完全改善)。在第16周和第52周,分别有52.4%和30.8%的患者实现了内镜缓解。UC内镜严重程度指数是评估结肠炎症严重程度的内镜指数之一,基线得分越高,与临床反应(即症状部分改善)呈负相关。19名患者(12.8%)发生了带状疱疹和深静脉血栓等不良事件,12名患者(8.1%)发生了严重不良事件。我们的实际研究表明,托法替尼对韩国UC患者是一种临床有效的治疗方法,其不良反应发生率也与其他实际研究中观察到的不良反应发生率相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology Medicine-Gastroenterology
自引率
2.40%
发文量
103
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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