University of California San Francisco, Department of Medicine, Division of Gastroenterology, San Francisco, CA, USA.
J Crohns Colitis. 2020 Jul 30;14(7):1026-1028. doi: 10.1093/ecco-jcc/jjaa018.
Acute severe ulcerative colitis is a high stakes event with significant numbers still requiring emergent colectomy, representing a need to establish alternative medical management options. We report a case series of tofacitinib as rescue therapy in biologic-experienced patients with acute severe ulcerative colitis.
Four patients were identified over a 1-year period at our institution who initiated tofacitinib for acute severe ulcerative colitis. All four had previously failed at least two biologics, including infliximab, and were failing high-dose oral prednisone therapy before admission. All patients had Mayo disease activity index of at least 10 at admission. After no significant improvement despite receiving a minimum of 3 days of intravenous methylprednisolone and based on elevated Ho and Travis indices at Day 3, patients were offered rescue tofacitinib for induction of remission, or colectomy. Standard induction of tofacitinib was used [10 mg twice daily], and one patient was escalated to 15 mg twice daily after inadequate response.
All patients experienced improvement in objective symptoms and laboratory markers, and were discharged without colectomy on tofacitinib as maintenance therapy and prednisone taper; 30-day and 90-day colectomy rates on tofacitinib maintenance therapy were zero and 90-day readmission rate was also zero. Two of four patients achieved steroid-free remission on maintenance tofacitinib monotherapy based on clinical symptoms and follow-up endoscopy. No major adverse reaction was reported during induction or maintenance therapy.
Tofacitinib may be an acceptable rescue agent in biologic-experienced patients with acute severe ulcerative colitis. Tofacitinib may also be safely continued as maintenance therapy once remission has been achieved.
急性重度溃疡性结肠炎是一个高风险事件,仍有大量患者需要紧急结肠切除术,这代表着需要建立替代的医学治疗方案。我们报告了一例托法替尼在生物制剂治疗经验丰富的急性重度溃疡性结肠炎患者中的治疗病例系列。
在我们的机构中,在过去的 1 年中确定了 4 例因急性重度溃疡性结肠炎而开始使用托法替尼的患者。所有 4 例患者均以前至少使用过两种生物制剂(包括英夫利昔单抗)治疗失败,并且在入院前正在接受大剂量口服泼尼松治疗但病情仍在进展。所有患者入院时的 Mayo 疾病活动指数均至少为 10。尽管接受了至少 3 天的静脉甲基泼尼松龙治疗,但在第 3 天根据 Ho 和 Travis 指数仍未见明显改善,故为患者提供托法替尼进行缓解诱导治疗,或进行结肠切除术。采用标准托法替尼诱导方案[每日两次 10mg],有 1 例患者因应答不足而升级至每日两次 15mg。
所有患者的客观症状和实验室标志物均有所改善,并在无结肠切除术的情况下出院,接受托法替尼维持治疗和泼尼松减量;托法替尼维持治疗的 30 天和 90 天结肠切除术率均为 0,90 天再入院率也为 0。4 例患者中有 2 例在托法替尼维持治疗时根据临床症状和随访内镜检查达到无激素缓解。诱导或维持治疗期间未报告重大不良反应。
托法替尼可能是生物制剂治疗经验丰富的急性重度溃疡性结肠炎患者的一种可接受的补救药物。一旦缓解,托法替尼也可以安全地作为维持治疗继续使用。