首页|乌司奴单抗治疗克罗恩病的短期疗效和安全性:一项单中心真实世界研究

乌司奴单抗治疗克罗恩病的短期疗效和安全性:一项单中心真实世界研究

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背景:全球克罗恩病(CD)疾病负担呈上升趋势.乌司奴单抗(UST)治疗CD的疗效和安全性需要进一步验证.目的:评估UST治疗CD的短期疗效和安全性.方法:本研究为单中心回顾性观察性研究,采集昆明医科大学第一附属医院2020年1月—2023年12月接受UST治疗的CD患者的临床资料进行分析.分别以克罗恩病活动指数(CDAI)和简化克罗恩病内镜下评分(SES-CD)评估临床和内镜下疾病活动度.主要结局指标为临床应答率和临床缓解率(CDAI<150分定义为临床缓解,下降≥70分或下降<70分但总分<150分为临床应答);次要结局指标包括内镜应答率和内镜缓解率(SES-CD≤2分定义为内镜缓解,下降≥50%为内镜应答),以及炎症、营养指标变化和不良事件发生情况.结果:共27例CD患者纳入研究,男性16例,女性11例,中位病程3.00年.UST治疗后16/20周和32周,中位CDAI评分较基线值显著下降[129.83(89.67,151.33)分和95.07(67.45,178.34)分对213.00(178.83,302.98)分,P均<0.017],临床应答率分别为92.6%和95.5%,临床缓解率分别为70.4%和72.7%.按既往是否使用过生物制剂和是否采用优化治疗分层分析,亚组间临床应答率和临床缓解率差异均无统计学意义.17例患者于16/20周复查结肠镜,SES-CD较基线值显著下降[(5.47±4.53)分对(9.88±4.58)分,P<0.05],内镜应答率和内镜缓解率分别为35.3%和23.5%.16/20周和32周C反应蛋白均较基线值显著下降(P均<0.017),血小板计数、血红蛋白、白蛋白、体质指数亦有改善趋势,但差异无统计学意义.用药期间未观察到严重不良事件.结论:UST能在短期内有效改善CD患者的临床症状和内镜下表现,减轻全身炎症负荷,且具有较好的安全性.
Short-term Efficacy and Safety of Ustekinumab in Treatment of Crohn's Disease:A Single-center Real-world Study
Background:The burden of Crohn's disease(CD)is rising globally,and the efficacy and safety of ustekinumab(UST)in treatment of CD need to be further verified.Aims:To assess the short-term efficacy and safety of UST in CD patients.Methods:A single-center retrospective observational study was conducted in the First Affiliated Hospital of Kunming Medical University.The clinical data of CD patients treated with UST from January 2020 to December 2023 were analyzed retrospectively.The clinical activity and endoscopic severity of the disease were assessed using Crohn's disease activity index(CDAI)and simple endoscopic score for Crohn's disease(SES-CD),respectively.The primary outcomes were clinical response(CDAI score decreased≥70 points,or CDAI score decreased<70 points but the total score<150)and clinical remission(CDAI score<150),while the secondary outcomes included endoscopic response(SES-CD decreased≥50%),endoscopic remission(SES-CD≤2),changes of inflammatory and nutritional indicators,and the adverse events.Results:Twenty-seven CD patients were included,of which,16 were males,and 11 were females,with median disease duration of 3.00 years.After treatment with UST,the median CDAI score decreased from 213.00(178.83,302.98)at baseline to 129.83(89.67,151.33)at week 16/20 and 95.07(67.45,178.34)at week 32(all P<0.017).The clinical response rate and remission rate at week 16/20 were 92.6%and 70.4%,respectively,and those at week 32 were 95.5%and 72.7%,respectively.When patients were stratified as biologic naïve and exposure,or as with and without dose optimization,no significant differences were found in clinical response and remission rates among various subgroups.Seventeen patients reviewed endoscopy at week 16/20,the SES-CD decreased significantly from baseline(5.47±4.53 vs.9.88±4.58,P<0.05),with the endoscopic response rate and remission rate of 35.3%and 23.5%,respectively.C-reactive protein decreased significantly from baseline at week 16/20 and week 32 of treatment(all P<0.017),while the platelet count,hemoglobin,albumin and body mass index only showed insignificant improving trends.No serious adverse events were observed during the medication period.Conclusions:UST can improve the clinical symptoms,endoscopic manifestations,and systemic inflammation effectively in CD patients in short-term follow-up,and represents a good safety profile.

UstekinumabCrohn DiseaseShort-Term EfficacySafety

陈杞殷、罗娟、董明志、张瀚予、刘晓琳、陈紫红、缪应雷

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昆明医科大学第一附属医院消化内科(650032)

云南省消化系统疾病临床医学研究中心

云南省保山市第二人民医院消化内科

乌司奴单抗 Crohn病 短期疗效 安全性

2024

胃肠病学
上海交通大学医学院附属仁济医院

胃肠病学

CSTPCD
影响因子:1.217
ISSN:1008-7125
年,卷(期):2024.29(5)