类固醇难治性急性重症溃疡性结肠炎患者接受环孢素诱导和乌司替尼维持联合疗法的长期疗效。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2023-12-30 eCollection Date: 2024-01-01 DOI:10.1177/17562848231218555
Francesco Vitali, Timo Rath, Entcho Klenske, Anna-Lena Vögele, Ingo Ganzleben, Sebastian Zundler, Deike Strobel, Carol Geppert, Arndt Hartmann, Markus F Neurath, Raja Atreya
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引用次数: 0

摘要

背景:有效治疗急性重度溃疡性结肠炎(ASUC)患者是一项重大挑战,在环孢素诱导治疗有效后,可用的维持治疗方案仍然很少:我们研究了环孢素和乌司他单抗联合疗法对类固醇难治性ASUC患者的长期有效性和安全性:单中心、前瞻性研究:我们纳入了既往多次晚期治疗失败的类固醇难治性ASUC患者,他们接受了环孢素和乌斯特库单抗联合治疗:结果:在纳入的11名患者中,10人曾因使用英夫利西单抗而失败,8人曾至少三次使用生物疗法失败。梅奥和Lichtiger评分的平均基线分别为10.9(9-12)分和13.3(11-14)分。Ustekinumab 在环孢素治疗开始后 3.2 周(1-8 周)开始使用,联合治疗平均持续 11.5 周(4-20 周)。有 6 名患者在第 16 周时获得了临床应答,有 5 名患者在第 48 周时获得了无类固醇临床缓解。第 16 周时,5 名患者获得内镜缓解,第 52 周时,5 名患者获得组织学缓解。肠道超声显示,乙状结肠肠壁平均增厚程度在基线时为 5.5 毫米,在第 52 周时为 3.5 毫米。两名患者不得不接受结肠切除术(平均时间为 4.5 个月,范围为 3-6 个月),三名患者因疗效不佳而停止了乌斯特库单抗治疗。总体而言,联合疗法的耐受性良好:结论:环孢素和乌斯特库单抗联合疗法可使近一半的ASUC患者在52周后达到临床和内镜缓解,值得进一步研究:试验注册:不适用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term outcomes of cyclosporin induction and ustekinumab maintenance combination therapy in patients with steroid-refractory acute severe ulcerative colitis.

Background: Effective management of patients with acute severe ulcerative colitis (ASUC) is a major challenge and there remains a paucity of available maintenance treatment options after efficacious cyclosporin induction therapy.

Objectives: We investigated the long-term effectiveness and safety of cyclosporin and ustekinumab combination therapy in patients with steroid refractory ASUC.

Design: Monocentric, prospective study.

Methods: We included patients with steroid refractory ASUC with multiple failed prior advanced therapies, who were treated with cyclosporin and ustekinumab combination therapy.

Results: Among the 11 included patients, 10 had prior failure to infliximab and 8 failed at least three previous biological therapies. The mean baseline Mayo and Lichtiger scores were 10.9 (9-12) and 13.3 (11-14), respectively. Ustekinumab was initiated 3.2 weeks (1-8) after initiation of cyclosporin treatment and combination therapy was continued for a mean of 11.5 (4-20) weeks. Clinical response was achieved in six patients at week 16 and clinical steroid-free clinical remission in five patients at week 48. Endoscopic remission was achieved in five patients at week 16 and together with histological remission in five patients at week 52. Intestinal ultrasound demonstrated mean bowel wall thickening in the sigmoid colon of 5.5 mm at baseline and 3.5 mm at week 52, respectively. Two patients had to undergo colectomy (mean 4.5 months, range 3-6) and three stopped ustekinumab therapy due to ineffectiveness. Overall, combination therapy was well tolerated.

Conclusion: Combination of cyclosporin and ustekinumab therapy allowed nearly half of ASUC patients to reach clinical and endoscopic remission after 52 weeks, warranting further studies.

Trial registration: Not applicable.

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