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联合组织学和内镜终点与乌司奴单抗治疗溃疡性结肠炎患者疗效的关系。

Relationship Between Combined Histologic and Endoscopic Endpoints and Efficacy of Ustekinumab Treatment in Patients With Ulcerative Colitis.

机构信息

Immunology Translational Science, Janssen Research & Development, LLC, Spring House, Pennsylvania.

Immunology, Janssen Research & Development, LLC, Spring House, Pennsylvania.

出版信息

Gastroenterology. 2020 Dec;159(6):2052-2064. doi: 10.1053/j.gastro.2020.08.037. Epub 2020 Aug 25.

Abstract

BACKGROUND & AIMS: Ustekinumab induces and maintains histologic improvement in patients with ulcerative colitis (UC). The clinical relevance of this endpoint alone, and in combination with endoscopic improvement, is unknown.

METHODS

Histologic disease activity was evaluated in 2630 colonic biopsy samples from patients with UC treated in the UNIFI phase 3 UC clinical studies of ustekinumab. We evaluated associations between histologic improvement (defined as the composite of neutrophil infiltration in less than 5% of crypts and no crypt destruction, erosions, ulcerations, or granulation tissue) and clinical endpoints at the end of induction (week 8 and 16) and maintenance (week 44) periods. We assessed the validity of a combined histologic and endoscopic (Mayo endoscopy subscore, 0 or 1) improvement endpoint, which we called histo-endoscopic mucosal healing (or histo-endoscopic mucosal improvement).

RESULTS

Histologic improvement was significantly (P < .0001) associated with clinical remission, lower mean disease activity scores, and greater improvement in disease activity at the end of induction and maintenance studies. Ustekinumab induced and maintained significantly higher rates of histologic improvement at induction week 8 and maintenance week 44 than placebo when more stringent definitions of histologic improvement were used. Histologic improvement and endoscopic improvement following induction were associated with 10% to 20% higher rates of histo-endoscopic mucosal healing, clinical remission, and corticosteroid-free remission at week 44 (all P < .05) in patients who received ustekinumab maintenance therapy. At week 44, 61% of patients (56/92) with histo-endoscopic mucosal healing after induction therapy achieved clinical remission, versus 39% of patients (9/23, P = .0983) and 34% of patients (24/71, P = .0009) with endoscopic or histologic improvement alone after induction, respectively.

CONCLUSION

Data from the UNIFI program of ustekinumab in patients with UC treated with ustekinumab indicated the achievement of histo-endoscopic mucosal healing after induction therapy is associated with lower disease activity at the end of maintenance therapy than either histologic or endoscopic improvement alone. ClinicalTrials.gov number: NCT02407236.

摘要

背景与目的

乌司奴单抗可诱导并维持溃疡性结肠炎(UC)患者的组织学改善。目前尚不清楚该终点的临床相关性,以及与内镜改善相结合的临床相关性。

方法

在乌司奴单抗治疗 UC 的 UNIFI 3 期临床试验中,对 2630 例结肠活检样本进行了组织学疾病活动评估。我们评估了诱导期(第 8 周和第 16 周)和维持期(第 44 周)结束时组织学改善(定义为隐窝内中性粒细胞浸润少于 5%,无隐窝破坏、糜烂、溃疡或肉芽组织)与临床终点之间的关联。我们评估了组织学和内镜(Mayo 内镜亚评分 0 或 1)改善终点(我们称之为组织内镜黏膜愈合或组织内镜黏膜改善)的有效性。

结果

组织学改善与临床缓解、较低的平均疾病活动评分以及诱导和维持研究结束时疾病活动的更大改善显著相关(P <.0001)。当使用更严格的组织学改善定义时,乌司奴单抗在诱导第 8 周和维持第 44 周诱导和维持组织学改善的发生率显著高于安慰剂。诱导后组织学和内镜改善与 10%至 20%更高的组织内镜黏膜愈合、临床缓解和无皮质类固醇缓解率相关在接受乌司奴单抗维持治疗的患者中,第 44 周(所有 P <.05)。在诱导治疗后达到组织内镜黏膜愈合的患者中,61%(56/92)在第 44 周达到临床缓解,而诱导后仅内镜或组织学改善的患者分别为 39%(9/23,P =.0983)和 34%(24/71,P =.0009)。

结论

来自接受乌司奴单抗治疗的 UC 患者的 UNIFI 计划的数据表明,诱导治疗后达到组织内镜黏膜愈合与维持治疗结束时较低的疾病活动相关,而不是单独的组织学或内镜改善。临床试验编号:NCT02407236。

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