Patients with ulcerative colitis who have normalized histology are clinically stable after de-escalation of therapy

Shintaro Akiyama, Joëlle St-Pierre, Cindy Traboulsi, Alexa Silfen, Victoria Rai, Tina G. Rodriguez, Amarachi I. Erondu, Joshua M. Steinberg, Seth R. Shaffer, Britt Christensen, David T. Rubin
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Abstract

We have previously demonstrated that histological normalization in ulcerative colitis (UC) is associated with superior maintenance of remission outcomes. This single-center, retrospective case-control study assessed outcomes after the therapeutic de-escalation in UC patients who have achieved histologic normalization. A total of 111 patients were included, of which 24 underwent de-escalation, and 87 patients without therapeutic changes. The most commonly withdrawn therapy was aminosalicylates (50%), followed by immunomodulators (37.5%), and biologics (12.5%). Fourteen patients remained on therapies after de-escalation, including aminosalicylate (9/14), immunomodulators (3/14), and biologics (3/14), while 10 patients were not on any therapy immediately after withdrawal. Median follow-up was 43 months in the de-escalation group and 47 months in the control. The rates of clinical, endoscopic, and histologic recurrence were not significantly different between the two groups, nor was the proportion of patients who subsequently required additional therapies after withdrawal (P = 0.133). Clinical and endo-histologic recurrence rates were the lowest in patients who withdrew immunomodulators (0% and 14.3%, respectively). We demonstrate the clinical stability of therapeutic withdrawal in UC patients with histologic normalization.

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组织学正常化的溃疡性结肠炎患者在放弃治疗后临床症状稳定
我们曾证实,溃疡性结肠炎(UC)组织学正常化与良好的缓解维持效果相关。这项单中心、回顾性病例对照研究评估了已实现组织学正常化的 UC 患者接受治疗降级后的疗效。研究共纳入111名患者,其中24人接受了降级治疗,87人未接受治疗改变。最常停用的疗法是氨基水杨酸盐(50%),其次是免疫调节剂(37.5%)和生物制剂(12.5%)。14名患者在停药后仍在接受治疗,包括氨基水杨酸盐(9/14)、免疫调节剂(3/14)和生物制剂(3/14),而10名患者在停药后没有立即接受任何治疗。停药组的中位随访时间为 43 个月,对照组为 47 个月。两组患者的临床、内镜和组织学复发率无显著差异,停药后需要额外治疗的患者比例也无显著差异(P = 0.133)。停用免疫调节剂的患者临床复发率和内镜组织学复发率最低(分别为 0% 和 14.3%)。我们证明了 UC 患者停药后组织学正常化的临床稳定性。
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