Adalimumab and Infliximab Are Equally Effective for Crohn's Disease in Patients Not Previously Treated With Anti-Tumor Necrosis Factor-α Agents

被引:68
|
作者
Kestens, Christine [1 ]
van Oijen, Martijn G. H. [1 ,2 ]
Mulder, Charlotte L. J. [1 ]
van Bodegraven, Ad A. [3 ]
Dijkstra, Gerard [4 ]
de Jong, Dirk [5 ]
Ponsioen, Cyriel [6 ]
van Tuyl, Bas A. C. [7 ]
Siersema, Peter D. [1 ]
Fidder, Herma H. [1 ]
Oldenburg, Bas [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, NL-3584 CX Utrecht, Netherlands
[2] Univ Calif Los Angeles, David Geffen Sch Med, Div Digest Dis, Los Angeles, CA 90095 USA
[3] Vrije Univ Amsterdam, Med Ctr, Amsterdam, Netherlands
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Dept Gastroenterol & Hepatol, NL-6525 ED Nijmegen, Netherlands
[6] Amsterdam Med Ctr, Dept Gastroenterol & Hepatol, Amsterdam, Netherlands
[7] Diakonessenhuis Hosp, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
关键词
Crohn; Anti-TNF alpha; Infliximab; Adalimumab; Response; INFLAMMATORY-BOWEL-DISEASE; DOSE INTENSIFICATION; CO-TREATMENT; MAINTENANCE; THERAPY; REMISSION; TERM; PREDICTORS; ANTIBODY; BENEFIT;
D O I
10.1016/j.cgh.2013.01.012
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Infliximab (IFX) and adalimumab (ADA) are thought to have equal efficacy for the treatment of Crohn's disease (CD), although no direct comparison has been performed. We compared the effectiveness and safety of IFX and ADA in carefully matched cohorts. METHODS: We performed a retrospective cohort study of 200 patients with CD (100 treated with IFX and 100 treated with ADA, starting in 2006 or later) who had not received anti-tumor necrosis factor alpha agents previously; the patients were identified from databases of 6 hospitals in The Netherlands. The groups were matched carefully for indication, duration of disease, age, and Montreal classification. The primary end point was the steroid-free clinical response, defined by a combination of multiple clinical parameters, after 1 year. RESULTS: Of the total patient population, 63.5% and 45% had a clinical response after 1 and 2 years, respectively. There were no significant differences between treatment groups: at 1 and 2 years, 62% and 41% of those receiving ADA vs 65% and 49% of those receiving IFX had responses, respectively. Kaplan-Meier curves showed identical decreases in response rates over time. Combining IFX or ADA with immunomodulator therapy was associated with a higher clinical response than monotherapy, although this was only significant among patients who received IFX (P = .03). There were no differences in numbers of side effects or opportunistic infections. CONCLUSIONS: The effectiveness of ADA or IFX treatment in anti-tumor necrosis factor alpha-naive patients with CD is comparable after 1 and 2 years of follow-up evaluation. The efficacies of IFX and ADA each seem to increase when given with immunomodulator therapy, although only significantly for IFX.
引用
收藏
页码:826 / 831
页数:6
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