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托法替布治疗溃疡性结肠炎患者的真实疗效及安全性:一项KASID多中心队列研究

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

作者信息

Shin Seung Hwan, Oh Kyunghwan, Hong Sung Noh, Lee Jungbok, Oh Shin Ju, Kim Eun Soo, Na Soo-Young, Kang Sang-Bum, Koh Seong-Joon, Bang Ki Bae, Jung Sung-Ae, Jung Sung Hoon, Kim Kyeong Ok, Park Sang Hyoung, Yang Suk-Kyun, Choi Chang Hwan, Ye Byong Duk

机构信息

Department of Gastroenterology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

Division of Gastroenterology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Therap Adv Gastroenterol. 2023 Mar 18;16:17562848231154103. doi: 10.1177/17562848231154103. eCollection 2023.

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,  = 0.029] and corticosteroid-free clinical response (aOR: 0.782,  = 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

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.

摘要

背景

托法替布是一种抑制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,关于托法替布在亚洲UC患者中的真实数据有限。

目的

探讨托法替布诱导和维持治疗对韩国UC患者的真实疗效和安全性。

设计

这是一项对2018年1月至2020年11月期间在韩国12家医院接受托法替布治疗的UC患者的回顾性研究。

方法

将第52周时临床缓解定义为梅奥评分(Mayo score)总分≤2分,直肠出血分项评分与排便频率分项评分之和≤1分,并将其作为主要观察指标。还评估了不良事件(AE),包括带状疱疹和深静脉血栓形成。

结果

共有148例UC患者开始使用托法替布治疗。第16周、24周和52周的临床缓解率分别为60.6%、54.9%和52.8%。第16周、24周和52周的临床缓解率分别为71.8%、67.6%和59.9%。基于梅奥内镜分项评分,第16周和第52周的内镜缓解率分别为52.4%和30.8%;基于溃疡性结肠炎内镜严重程度指数(UCEIS),第16周和第52周的内镜缓解率分别为20.7%和15.2%。基线时较高的UCEIS与第52周时的临床缓解(校正比值比[aOR]:0.774,P = 0.029)和无皮质类固醇临床缓解(aOR:0.782,P = 0.035)呈负相关。19例患者(12.8%)发生AE,12例患者(8.1%)发生严重AE。4例患者(2.7%)发生带状疱疹。1例患者(0.7%)发生深静脉血栓形成。

结论

托法替布对韩国UC患者是一种有效的诱导和维持治疗药物,安全性可接受。

通俗易懂的总结

溃疡性结肠炎(UC)是一种结肠黏膜特发性慢性炎症性疾病,通常表现为血性腹泻和腹痛。托法替布是一种抑制Janus激酶的小分子药物,据报道对西方UC患者有效。然而,关于托法替布在亚洲UC患者中疗效的真实数据有限。为了研究托法替布治疗韩国UC患者的真实疗效和安全性,我们回顾性分析了2018年1月至2020年11月期间在韩国12家医院接受托法替布治疗的148例UC患者的数据。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)。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标之一,基线时较高的该指数与临床缓解(即症状部分改善)呈负相关。19例患者(12.8%)发生了包括带状疱疹和深静脉血栓形成在内的不良事件(AE),12例患者(8.1%)发生了严重AE。我们的真实研究表明,托法替布对韩国UC患者是一种临床有效的治疗药物,AE的发生率也与其他真实世界研究中观察到的相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7824/10026122/26b226fd22aa/10.1177_17562848231154103-fig1.jpg

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