Impact of Concomitant Corticosteroids on Tofacitinib Induction Efficacy and Infection Rates in Ulcerative Colitis

被引:1
|
作者
Lichtenstein, Gary R. [1 ]
Cohen, Benjamin L. [2 ]
Salese, Leonardo [3 ]
Modesto, Irene [4 ]
Wang, Wenjin [3 ]
Chan, Gary [3 ]
Ahmed, Haytham Mohamed [5 ]
Su, Chinyu [3 ]
Peyrin-Biroulet, Laurent [6 ]
机构
[1] Univ Penn, Div Gastroenterol, Perelman Sch Med, Philadelphia, PA USA
[2] Cleveland Clin, Digest Dis & Surg Inst, Dept Gastroenterol, Cleveland Hts, OH USA
[3] Pfizer Inc, Collegeville, PA USA
[4] Pfizer Inc, 235 East 42nd St, New York, NY 10017 USA
[5] Pfizer Inc, Dubai, U Arab Emirates
[6] Univ Lorraine, Nancy Univ Hosp, Dept Gastroenterol, Inserm NGERE U1256, Vandoeuvre Les Nancy, France
关键词
Induction therapy; Infections; Corticosteroid; Janus kinase inhibitor; SERIOUS INFECTION; RHEUMATOID-ARTHRITIS; HERPES-ZOSTER; RISK-FACTORS; THERAPY; DISEASE; SAFETY;
D O I
10.1007/s10620-022-07794-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Tofacitinib is an oral small molecule Janus kinase inhibitor for the treatment of ulcerative colitis.Aim To report efficacy and infection rates in patients receiving tofacitinib induction treatment, by baseline corticosteroid status.Methods We evaluated efficacy and safety data from OCTAVE Induction 1&2 in patients with moderately-to-severely active ulcerative colitis who received tofacitinib 10 mg twice daily or placebo for 8 weeks, based on induction baseline oral corticosteroid use (Corticosteroid-Yes/No) and dose (< 20/ =20 mg/day). Infections of interest included serious infections, herpes zoster (HZ), and adjudicated opportunistic infections (OIs).Results At OCTAVE Induction 1&2 baseline, 478/1092 (43.8%) patients were receiving corticosteroids. Tofacitinib demonstrated significant induction efficacy versus placebo for both Corticosteroid-Yes and Corticosteroid-No. With adjustment for prior tumor necrosis factor inhibitor and immunosuppressant failure, there were no statistically significant differences in remission and clinical response rates for Corticosteroid-Yes versus Corticosteroid-No. Among tofacitinib-treated patients, HZ and OIs occurred more frequently in Corticosteroid-Yes versus Corticosteroid-No, regardless of dose (< 20 mg vs. = 20 mg). Infection incidence rates (regardless of severity/seriousness) during tofacitinib induction were generally similar regardless of baseline corticosteroid use. The proportion of tofacitinib-treated patients with HZ was 0.2% for Corticosteroid-No versus 1.1% for Corticosteroid-Yes < 20 mg and 1.0% for Corticosteroid-Yes = 20 mg. Two out of three patients had HZ OIs.Conclusions Tofacitinib induction efficacy (clinical response and remission) was similar in baseline corticosteroid subgroups. Infections of interest were rare; HZ and OIs occurred more frequently among those receiving tofacitinib and corticosteroids versus those receiving tofacitinib without corticosteroids.
引用
收藏
页码:2624 / 2634
页数:11
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