Efficacy and safety of filgotinib for ulcerative colitis: A real-world multicenter retrospective study in Japan

被引:11
|
作者
Akiyama, Shintaro [1 ]
Yokoyama, Kaoru [2 ]
Yagi, Soichi [3 ]
Shinzaki, Shinichiro [3 ]
Tsuruta, Kozo [4 ]
Yoshioka, Shinichiro [4 ]
Sako, Minako [5 ]
Shimizu, Hiromichi [6 ]
Kobayashi, Mariko [1 ]
Sakurai, Toshiyuki [7 ]
Nomura, Kei [8 ]
Shibuya, Tomoyoshi [8 ]
Takahara, Masahiro [9 ]
Hiraoka, Sakiko [9 ]
Sugai, Kyohei [10 ]
Yanai, Shunichi [10 ]
Yoshida, Atsushi [11 ]
Koroku, Miki [12 ]
Omori, Teppei [12 ]
Saruta, Masayuki [7 ]
Matsumoto, Takayuki [10 ]
Okamoto, Ryuichi [6 ]
Tsuchiya, Kiichiro [1 ]
Fujii, Toshimitsu [6 ,13 ]
机构
[1] Univ Tsukuba, Inst Med, Dept Gastroenterol, Ibaraki, Japan
[2] Kitasato Univ, Sch Med, Dept Gastroenterol, Sagamihara, Kanagawa, Japan
[3] Hyogo Med Univ, Fac Med, Dept Gastroenterol, Nishinomiya, Hyogo, Japan
[4] Kurume Univ, Sch Med, Dept Med, Div Gastroenterol, Fukuoka, Japan
[5] Japan Community Healthcare Org, Ctr Inflammatory Bowel Dis, Tokyo Yamate Med Ctr, Tokyo, Japan
[6] Tokyo Med & Dent Univ, Dept Gastroenterol & Hepatol, Tokyo, Japan
[7] Jikei Univ, Sch Med, Dept Internal Med, Div Gastroenterol & Hepatol, Tokyo, Japan
[8] Juntendo Univ, Sch Med, Dept Gastroenterol, Tokyo, Japan
[9] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Gastroenterol & Hepatol, Okayama, Japan
[10] Iwate Med Univ, Sch Med, Dept Internal Med, Div Gastroenterol & Hepatol, Morioka, Iwate, Japan
[11] Ofuna Chuo Hosp, Ctr Gastroenterol & Inflammatory Bowel Dis, Kamakura, Kanagawa, Japan
[12] Tokyo Womens Med Univ, Inst Gastroenterol, Tokyo, Japan
[13] Tokyo Med & Dent Univ, Dept Gastroenterol & Hepatol, Bunkyo Ku, Tokyo, Japan
关键词
INFLAMMATORY-BOWEL-DISEASE; DOUBLE-BLIND; THERAPY;
D O I
10.1111/apt.17961
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimsWhile filgotinib, an oral Janus kinase (JAK) 1 preferential inhibitor, is approved for moderately to severely active ulcerative colitis (UC), real-world studies assessing its short- and long-term efficacy and safety are limited.MethodsThis is a multicenter, retrospective study of UC patients who started filgotinib between March 2022 and September 2023. The primary outcome was clinical remission, defined as a partial Mayo score <= 1 with a rectal bleeding score of 0, or Simple Clinical Colitis Activity Index (SCCAI) <= 2 with a blood-in-stool score of 0. Secondary outcomes included clinical response, corticosteroid-free remission, and endoscopic improvement. Outcomes were assessed at 10, 26, and 58 weeks based on patients with available follow-up. Adverse events were evaluated.ResultsWe identified 238 UC patients and 54% had prior exposure to biologics/JAK inhibitors. The median baseline partial Mayo score and SCCAI were 5 (IQR 3-6) and 4 (IQR 2-7). Clinical remission rates based on per-protocol analysis at 10, 26, and 58 weeks were 47% (70/149), 55.8% (48/86), and 64.6% (31/48), respectively. At a median follow-up of 28 weeks (IQR 10-54) with a discontinuation rate of 39%, the rates of clinical remission, clinical response, corticosteroid-free remission, and endoscopic improvement were 39.9% (81/203), 54.7% (111/203), and 36.5% (74/203), and 43.5% (10/23), respectively. These rates were comparable between biologic/JAK inhibitor-naive and -experienced patients. While three patients (1.3%) developed herpes zoster infection, no cases of thrombosis or death were reported.ConclusionsReal-world data demonstrate favourable clinical and safety outcomes of filgotinib for UC. A real-world multicenter retrospective study in Japan shows favourable clinical and safety outcomes of filgotinib for ulcerative colitis (UC). Filgotinib provides good efficacy for UC patients with milder disease and retains efficacy even in biologic/Janus kinase inhibitor-experienced patients. Its upfront use may be preferred.image
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收藏
页码:1413 / 1424
页数:12
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