Sequential Use of High-Dose Tofacitinib After Infliximab Salvage Therapy in Acute Severe Ulcerative Colitis

J Crohns Colitis. 2022 Jan 28;16(1):166-168. doi: 10.1093/ecco-jcc/jjab109.

Abstract

Background and aims: Preliminary data regarding the effectiveness of tofacitinib in acute severe ulcerative colitis [ASUC] have been presented in two previous case series. We aimed to describe the novel use of high-dose tofacitinib immediately following non-response to infliximab in the setting of steroid-refractory ASUC.

Methods: Five patients who received high-dose tofacitinib 10 mg three times a day immediately following non-response to infliximab for steroid-refractory ASUC were identified at an Australian tertiary inflammatory bowel disease centre.

Results: Four of the five patients demonstrated clinical response to high-dose tofacitinib induction during their inpatient admission, with one patient requiring colectomy owing to a lack of clinical response. At 90 days, all four initial responders remained colectomy-free, with two patients achieving combined clinical and endoscopic remission. No adverse events directly attributable to high-dose tofacitinib were identified.

Conclusions: High-dose tofacitinib may have a role as salvage therapy in the setting of steroid-refractory ASUC. Prospective studies are required to determine the safety and efficacy of high-dose tofacitinib to determine whether it can be routinely recommended as primary or sequential salvage therapy in the setting of steroid-refractory ASUC.

Keywords: Acute severe ulcerative colitis; infliximab; tofacitinib.

MeSH terms

  • Adolescent
  • Adult
  • Australia
  • Colitis, Ulcerative / drug therapy*
  • Gastrointestinal Agents / therapeutic use*
  • Humans
  • Infliximab / therapeutic use*
  • Janus Kinase Inhibitors / therapeutic use*
  • Male
  • Piperidines / therapeutic use*
  • Pyrimidines / therapeutic use*
  • Salvage Therapy
  • Severity of Illness Index

Substances

  • Gastrointestinal Agents
  • Janus Kinase Inhibitors
  • Piperidines
  • Pyrimidines
  • tofacitinib
  • Infliximab