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巴利昔单抗治疗激素抵抗型溃疡性结肠炎:中重度疾病的更多经验

Basiliximab for the treatment of steroid-resistant ulcerative colitis: further experience in moderate and severe disease.

作者信息

Creed T J, Probert C S J, Norman M N, Moorghen M, Shepherd N A, Hearing S D, Dayan C M

机构信息

Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, Dorothy Hodgkin Building, Bristol, UK.

出版信息

Aliment Pharmacol Ther. 2006 May 15;23(10):1435-42. doi: 10.1111/j.1365-2036.2006.02904.x.

Abstract

BACKGROUND

Preliminary data have suggested that interleukin-2 receptor blockade with basiliximab may increase steroid sensitivity. We have previously reported a small case series demonstrating the potential of basiliximab as a novel agent for the treatment of steroid-resistant ulcerative colitis.

AIM

To report further experience of the efficacy and safety of treatment with the interleukin-2 receptor blocking monoclonal antibody basiliximab, in addition to steroids, for the treatment of severe and moderate steroid-resistant ulcerative colitis.

METHODS

Twenty patients were enrolled - 13 patients with moderate steroid-resistant ulcerative colitis (Ulcerative Colitis Symptom Score: >or=6) and seven patients with severe steroid-resistant ulcerative colitis. All were given a single dose of 40 mg basiliximab plus standard steroid therapy in an open-label, uncontrolled trial. Primary end point was clinical remission within 8 weeks (Ulcerative Colitis Symptom Score: <or=2).

RESULTS

Within 8 weeks, 10 of 20 (50%) patients achieved clinical remission (seven of 13 moderate, and three of seven severe). At 24 weeks, 13 of 20 (65%) patients were in clinical remission. Five patients required colectomy (four severe, one moderate ulcerative colitis) and one required rescue ciclosporin (moderate ulcerative colitis). Two patients developed herpes zoster, but treatment was generally well tolerated.

CONCLUSIONS

Basiliximab appears to promote prolonged remission after a single treatment. Taken in combination with previously reported data, basiliximab shows particular promise in moderate steroid-resistant ulcerative colitis.

摘要

背景

初步数据表明,使用巴利昔单抗阻断白细胞介素-2受体可能会增加类固醇敏感性。我们之前报告过一个小病例系列,证明了巴利昔单抗作为治疗类固醇抵抗性溃疡性结肠炎的新型药物的潜力。

目的

报告除类固醇外,使用白细胞介素-2受体阻断单克隆抗体巴利昔单抗治疗中重度类固醇抵抗性溃疡性结肠炎的疗效和安全性的进一步经验。

方法

招募了20名患者——13名中度类固醇抵抗性溃疡性结肠炎患者(溃疡性结肠炎症状评分:≥6)和7名重度类固醇抵抗性溃疡性结肠炎患者。在一项开放标签、非对照试验中,所有患者均接受一剂40mg巴利昔单抗加标准类固醇治疗。主要终点是8周内临床缓解(溃疡性结肠炎症状评分:≤2)。

结果

8周内,20名患者中有10名(50%)实现临床缓解(13名中度患者中有7名,7名重度患者中有3名)。24周时,20名患者中有13名(65%)处于临床缓解状态。5名患者需要进行结肠切除术(4名重度,1名中度溃疡性结肠炎),1名患者需要挽救性使用环孢素(中度溃疡性结肠炎)。2名患者发生带状疱疹,但治疗总体耐受性良好。

结论

巴利昔单抗单次治疗后似乎能促进长期缓解。结合先前报告的数据,巴利昔单抗在中度类固醇抵抗性溃疡性结肠炎中显示出特别的前景。

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