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维得利珠单克隆抗体治疗炎症性肠病患者的临床疗效分析

Analysis of clinical efficacy of vedolizumab in treatment of patients with inflammatory bowel disease

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目的 分析维得利珠单克隆抗体(VDZ)治疗炎症性肠病(IBD)患者的临床疗效.方法 选择 2021 年 2 月至 2022 年 5 月在空军军医大学第一附属医院接受VDZ治疗的 32 例IBD患者,分为溃疡性结肠炎(UC)组(n=25)和克罗恩病(CD)组(n=7).第 0、2、6、14、22、30、38、46、54 周分别给药 1次,随访至第 52 周.收集临床资料并进行分析.结果 在第 6、14、22 和 52 周时,UC组的临床应答率分别为 40.0%、68.0%、72.0%和 90.0%,临床缓解率分别为8.0%、16.0%、52.0%和 80.0%;CD组的临床应答率分别为 14.3%、71.4%、85.7%和 100%,临床缓解率分别为 0、42.9%、57.1%和 83.3%.在第 22、52 周,UC组的内镜应答率分别为 72.0%、90.0%,内镜缓解率分别为 64.0%、80.0%;CD组的内镜应答率分别为 71.4%、83.3%,内镜缓解率分别为 42.9%、83.3%.在第 6、14、22和 52 周,UC组的红细胞沉降率(ESR)、超敏C-反应蛋白(hs-CRP)、血小板计数(PLT)均较治疗前显著下降(P均<0.05),血红蛋白(HGB)均较治疗前显著升高(P均<0.05).在第6、14、22和52周,CD组的ESR均较治疗前显著下降(P均<0.05).在第6、52周,CD组的hs-CRP均较治疗前显著下降(P均<0.05).在第6、14 和 52 周,CD组的PLT均较治疗前显著下降(P均<0.05).在第 14、52 周,CD组的HGB均较治疗前显著升高(P均<0.05).随访期间仅 1 例患者出现过敏性皮疹,VDZ不良反应发生率为 3.1%.结论 VDZ能有效诱导及维持IBD疾病缓解,并且其不良反应发生率较低,安全性较高.
Objective This paper intends to analyze the clinical efficacy of vedolizumab(VDZ)in the treatment of patients with inflammatory bowel disease(IBD).Methods Thirty-two IBD patients who received VDZ treatment at the First Affiliated Hospital of Air Force Medical University from February 2021 to May 2022 were selected and divided into the ulcerative colitis(UC)group(n=25)and the Crohn's disease(CD)group(n=7).The patients were administered once in weeks 0,2,6,14,22,30,38,46,and 54,respectively,followed up until week 52,and the clinical data were collected and analyzed.Results At weeks 6,14,22,and 52,the clinical response rates of the UC group are 40.0%,68.0%,72.0%,and 90.0%,respectively,and the clinical remission rates are 8.0%,16.0%,52.0%,and 80.0%,respectively,while the clinical response rates of the CD group are 14.3%,71.4%,85.7%,and 100%,respectively,and the clinical remission rates are 0,42.9%,57.1%,and 83.3%,respectively.At weeks 22 and 52,the endoscopic response rates of the UC group are 72.0%and 90.0%,respectively,and the endoscopic remission rates are 64.0%and 80.0%,respectively,while the endoscopic response rates of the CD group are 71.4%and 83.3%,respectively,and the endoscopic remission rates are 42.9%and 83.3%,respectively.At weeks 6,14,22,and 52,compared with before treatment,the red blood cell sedimentation rate(ESR),hypersensitive C-reactive protein(hs-CRP),and platelet count(PLT)of the UC group are significantly decreased(P<0.05),while the hemoglobin(HGB)is significantly increased(P<0.05).At weeks 6,14,22,and 52,compared with before treatment,the ESR of the CD group is significantly decreased(P<0.05).At weeks 6 and 52,compared with before treatment,the hs-CRP of the CD group are significantly decreased(P<0.05).At weeks 6,14,and 52,compared with before treatment,the PLT of the CD group is significantly decreased(P<0.05).At weeks 14 and 52,compared with before treatment,the HGB of the CD group is significantly increased(P<0.05).During the follow-up period,only one patient developed allergic rash,and the incidence of VDZ adverse reactions is 3.1%.Conclusion VDZ can effectively induce and maintain remission of IBD,with a lower incidence of adverse reactions and higher safety.

VedolizumabInflammatory bowel diseaseUlcerative colitisCrohn's diseaseCurative effect

王玉龙、方洒、吴开春、时永全、梁洁、韩霜、陈敏

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710032 陕西西安,空军军医大学第一附属医院消化内科

710054 西安市红会医院消化内科

维得利珠单抗 炎症性肠病 溃疡性结肠炎 克罗恩病 疗效

2024

国际消化病杂志
上海市医学科学技术情报研究所

国际消化病杂志

CSTPCD
影响因子:0.796
ISSN:1673-534X
年,卷(期):2024.44(1)
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