Efficacy of Switching to Adalimumab for Maintenance of Remission Following Induction Therapy with Tacrolimus in Patients with Ulcerative Colitis

被引:2
|
作者
Numa, Keijiro [1 ]
Kakimoto, Kazuki [1 ]
Tanaka, Yasuyoshi [1 ]
Mizuta, Noboru [1 ]
Kinoshita, Naohiko [1 ]
Nakazawa, Kei [1 ]
Koshiba, Ryoji [1 ]
Hirata, Yuki [1 ]
Ota, Kazuhiro [1 ]
Miyazaki, Takako [1 ]
Nakamura, Shiro [1 ]
Higuchi, Kazuhide [1 ]
Nishikawa, Hiroki [1 ]
机构
[1] Osaka Med & Pharmaceut Univ, Dept Internal Med 2, 2-7 Daigakumachi, Takatsuki, Osaka 5698686, Japan
关键词
adalimumab; tacrolimus; ulcerative colitis; INFLAMMATORY-BOWEL-DISEASE; ENDOSCOPIC INDEX; CYCLOSPORINE; USTEKINUMAB; SAFETY;
D O I
10.3390/jcm12206699
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Tacrolimus (TAC) effectively induces remission in refractory ulcerative colitis (UC). However, TAC therapy usually lasts for 3 months. Although azathioprine (AZA) is often used in maintenance therapy, the relapse rate remains high. Herein, we evaluated the efficacy of adalimumab (ADA) for remission maintenance in patients with UC after induction therapy with TAC.Methods: We prospectively enrolled patients with moderate-to-severe UC who achieved clinical remission after 3 months of TAC therapy with endoscopic non-mucosal healing (Cohort A). After TAC discontinuation, the remission maintenance rate up to 1 year after starting ADA therapy was examined. We retrospectively enrolled patients with UC treated with TAC (Cohort B). Among patients in clinical remission after TAC treatment for 3 months, those who received AZA as remission maintenance therapy after TAC discontinuation constituted the AZA group. Patients in Cohort A who received ADA and AZA as remission maintenance therapy after TAC discontinuation constituted the ADA + AZA group. We compared the remission maintenance rates in the AZA and ADA + AZA groups for up to 5 years after TAC discontinuation. Results: In Cohort A, of the 46 patients with UC treated with TAC, 17 were eligible for analysis after receiving ADA as remission maintenance therapy. A notable 88.2% (15/17) were still in remission 1 year after starting ADA. The ADA + AZA group (n = 16) exhibited a significantly higher relapse-free rate than the AZA group (n = 26) (p < 0.05; log-rank test).Conclusion: switching to ADA for remission maintenance in patients with refractory UC who achieved clinical remission with TAC is clinically useful.
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页数:11
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