Serious Infection and Mortality in Patients With Crohn's Disease: More Than 5 Years of Follow-Up in the TREAT™ Registry

被引:574
作者
Lichtenstein, Gary R. [1 ]
Feagan, Brian G. [2 ,3 ]
Cohen, Russell D. [4 ]
Salzberg, Bruce A. [5 ]
Diamond, Robert H. [6 ]
Price, Samiyeh [6 ]
Langholff, Wayne [7 ]
Londhe, Anil [7 ]
Sandborn, William J. [8 ]
机构
[1] Univ Penn, Sch Med, Hosp Univ Penn, Div Gastroenterol,Dept Med, Philadelphia, PA 19104 USA
[2] Univ Western Ontario, Dept Epidemiol & Biostat, Robarts Res Inst, London, ON, Canada
[3] Univ Western Ontario, Dept Med, London, ON, Canada
[4] Univ Chicago, Med Ctr, Dept Med, Gastroenterol Sect, Chicago, IL 60637 USA
[5] Atlanta Gastroenterol Associates, Atlanta, GA USA
[6] Janssen Biotech Inc, Horsham, PA USA
[7] Johnson & Johnson PRD, Biostat, Edison, NJ USA
[8] Univ Calif San Diego, Div Gastroenterol, La Jolla, CA 92093 USA
关键词
INFLAMMATORY-BOWEL-DISEASE; NECROSIS FACTOR THERAPY; SAFETY; MANAGEMENT; INFLIXIMAB; COUNTY; DEATH; TNF;
D O I
10.1038/ajg.2012.218
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
OBJECTIVES: The objective of this study was to contribute long-term safety data for infliximab and other therapies in Crohn's disease (CD). METHODS: We prospectively evaluated CD patients enrolled in the large, observational Crohn's Therapy, Resource, Evaluation, and Assessment Tool registry, established to compare infliximab safety with conventional nonbiological medications in CD. RESULTS: A total of 6,273 patients were enrolled and evaluated on or before 23 February 2010; 3,420 received infliximab (17,712 patient-years; 89.9% received >= 2 infusions) and 2,853 received other-treatments-only (13,251 patient-years). Mean length of patient follow-up was 5.2 years. More infliximab-than other-treatments-only-treated patients had moderate-to-severe (30.6% vs. 10.7%) or severe-to-fulminant (2.5% vs. 0.6%) disease severity (P<0.001). In the year before enrollment, more infliximab-than other-treatments-only-treated patients required surgical intervention (17.4% vs. 13.6%), medical hospitalization (14.2% vs. 8.8%), prednisone (47.8% vs. 31.4%), immunomodulators (52.0% vs. 32.1%), and narcotic analgesics (17.3% vs. 9.1%). Patient mortality was similar for infliximab-and other-treatments-only-treated patients (0.58 vs. 0.59/100 patient-years). In multivariate logistic regression analyses, treatment with prednisone (hazard ratio (HR)=2.14, 95% confidence interval (CI)=1.55, 2.95; P<0.001) or narcotic analgesics (HR=1.79, 95% CI=1.29, 2.48; P<0.001) and age (HR=1.08, 95 % CI=1.07, 1.09; P<0.001) were associated with increased mortality risk. Neither infliximab nor immunomodulator treatment was associated with increased mortality risk. Factors independently associated with serious infections included moderate-to-severe disease activity (HR=2.24, 95 % CI=1.57, 3.19; P<0.001), narcotic analgesic treatment (HR=1.98, 95 % CI=1.44, 2.73; P<0.001), prednisone therapy (HR=1.57, 95 % CI=1.17, 2.10; P=0.002), and infliximab treatment (HR=1.43, 95 % CI=1.11, 1.84; P=0.006). CONCLUSIONS: Mortality was similar between infliximab- and other-treatments-only-treated CD patients. An increased risk of serious infection with infliximab was observed, although CD severity and use of prednisone or narcotic analgesics carried higher risks.
引用
收藏
页码:1409 / 1422
页数:14
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