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首页> 外文期刊>Scandinavian journal of gastroenterology. >Granulocyte-monocyte apheresis: an alternative combination therapy after loss of response to anti-TNF agents in ulcerative colitis
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Granulocyte-monocyte apheresis: an alternative combination therapy after loss of response to anti-TNF agents in ulcerative colitis

机译:粒细胞 - 单核细胞采血筛查:溃疡性结肠炎抗TNF试剂丧失后的替代联合疗法

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Objective: To evaluate the effectiveness and safety of the combination of granulocyte-monocyte apheresis (GMA) after loss of response (LOR) to anti-tumor necrosis factor (TNF) agents in ulcerative colitis (UC). Materials and methods: A retrospective, multicenter study was performed in 11 inflammatory bowel disease (IBD) Units. Clinical remission was defined as a partial Mayo score <= 2. The effectiveness of the treatment was evaluated by the partial Mayo score and the rate of anti-TNF intensification, switch, swap or colectomy. Results: Forty-seven patients with ulcerative colitis were included (mean age 35 years, mean disease duration 52 months, 66% male and 59% extensive colitis). Twenty-three subjects were receiving infliximab, eighteen adalimumab and six golimumab. GMA was combined after a primary non-response (49%) or secondary loss of response (51%) to anti-TNF therapy. We observed a significant decrease in partial Mayo score and fecal calprotectin after GMA. Fifteen patients (32%) responded to the combination therapy without anti-TNF intensification, switch, swap or colectomy. Eight patients (17%) underwent colectomy. Two patients (4%) presented adverse events related to the technique. Conclusions: Combination of GMA and anti-tumor necrosis factor is a safe and effective treatment after the loss of response to this biologic agents, with a significant decrease of the clinical disease activity and biomarkers, in a population with limited therapeutic alternatives.
机译:目的:评价粒细胞 - 单核细胞血液组合(GMA)在溃疡性结肠炎(UC)中抗肿瘤坏死因子(TNF)药物丧失后的粒细胞 - 单核细胞血细胞血细胞组合(GMA)组合的有效性和安全性。材料和方法:回顾性,在11个炎性肠病(IBD)单位中进行了多中心研究。临床缓解定义为部分玛雅得分<= 2.通过部分玛雅得分和抗TNF强化,开关,交换或联络术评估治疗的有效性。结果:包括溃疡性结肠炎的四十七名患者(平均35岁,平均疾病持续时间52个月,66%的男性和59%的结肠炎)。二十三个受试者接受英夫利昔单抗,十八令吉,六个Golimumab。在初级非反应(49%)或反应的二次丧失(51%)后,GMA合并为抗TNF疗法。在GMA之后,我们观察到部分Mayo评分和粪便钙保护菌素显着降低。十五名患者(32%)反应组合治疗,无抗TNF强化,开关,交换或联络术。八名患者(17%)接受了联络术。两名患者(4%)呈现与该技术有关的不良事件。结论:GMA和抗肿瘤坏死因子的组合是对这种生物药物的反应丧失后的安全有效的治疗,其临床疾病活性和生物标志物的显着降低,具有有限的治疗方法。

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