Abstract

Background and AimCombined therapy with tacrolimus (TAC) and an anti‐tumor necrosis factorα (TNFα) antibody is used to induce remission in ulcerative colitis (UC) patients who have not responded to monotherapy with either drug. We evaluated the efficacy and safety of combined therapy, as well as the relapse rate.MethodsCombined therapy was performed to induce remission in UC patients showing an inadequate response to monotherapy with TAC or an anti‐TNFα antibody. The following items were assessed retrospectively: (i) clinical characteristics, (ii) the remission induction rate, (iii) the relapse rate, and (iv) adverse events.ResultsCombined therapy induced remission in 7 of the 12 patients (58.3%). There were no significant differences in clinical characteristics between the patients with and without the successful induction of remission. However, the number of female patients tended to be higher in the remission group than in the nonremission group. The remission group also showed trends of a lower clinical activity index (Lichtiger index; CAI) on admission and before combined therapy and a lower total dose of prednisolone during hospitalization. The 1‐year relapse rate was 33.3%. Adverse events due to combined therapy included renal impairment (n = 2), tremors (n = 2), influenza (n = 1), and a positive cytomegalovirus antibody test (n = 3). None of these events were serious.ConclusionsCombined therapy was effective in more than half of the patients with refractory UC who had not responded to monotherapy. Our findings suggest that combination therapy may be a new, third option for the treatment of refractory UC.

Highlights

  • Treatment with tacrolimus (TAC) or anti-tumor necrosis factorα (TNFα) antibodies is effective as a remission induction therapy in patients with prednisolone (PSL)-dependent or PSL-resistant refractory ulcerative colitis (UC).[1]

  • In UC patients treated with adalimumab (ADA), another anti-TNFα biologic, the remission rate was 49.1%, and remission was maintained in 69.8% of patients at 52 weeks after induction.[5]

  • These results indicate that, in 40–50% of UC cases, remission is not achieved by monotherapy with TAC or an anti-TNFα antibody, and the longer-term outcome is not good

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Summary

Introduction

Treatment with tacrolimus (TAC) or anti-tumor necrosis factorα (TNFα) antibodies is effective as a remission induction therapy in patients with prednisolone (PSL)-dependent or PSL-resistant refractory ulcerative colitis (UC).[1] In UC patients receiving TAC therapy, the short-term remission rate was reported to be 52.6%, and the postrelapse colectomy rate was 69% at 1 year after the induction of remission.[2,3] In UC patients receiving infliximab (IFX), an anti-TNFα antibody, the short-term remission rate was 69%, and remission was maintained in 45% of patients at 54 weeks after induction.[4] In UC patients treated with adalimumab (ADA), another anti-TNFα biologic, the remission rate was 49.1%, and remission was maintained in 69.8% of patients at 52 weeks after induction.[5] These results indicate that, in 40–50% of UC cases, remission is not achieved by monotherapy with TAC or an anti-TNFα antibody, and the longer-term outcome is not good. Combined Tacrolimsu and anti-TNFα with TAC and an anti-TNFα antibody, as well as the relapse rate after such a therapy

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