Therapeutic Drug Monitoring to Guide Infliximab Dose Adjustment is Associated with Better Endoscopic Outcomes than Clinical Decision Making Alone in Active Inflammatory Bowel Disease

被引:78
作者
Kelly, Orlaith B. [1 ]
O'Donnell, Sarah [1 ]
Stempak, Joanne M. [1 ]
Steinhart, A. Hillary [1 ]
Silverberg, Mark S. [1 ]
机构
[1] Univ Toronto, Mt Sinai Hosp, Div Gastroenterol, Zane Cohen Ctr Digest Dis, Toronto, ON, Canada
关键词
therapeutic drug monitoring; infliximab; inflammatory bowel disease; LONG-TERM TREATMENT; CROHNS-DISEASE; ULCERATIVE-COLITIS; TROUGH LEVELS; ANTIBODIES; INTENSIFICATION; VALIDATION; INDUCTION; REMISSION; EFFICACY;
D O I
10.1097/MIB.0000000000001126
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Adequate infliximab (IFX) levels are associated with favorable outcomes in inflammatory bowel disease. Using therapeutic drug monitoring (TDM) to guide dosing is cost effective and associated with clinical improvement, but effect on endoscopic outcomes remains unclear. Methods: Primary responders to IFX who underwent dose escalation (2008-2014) were reviewed. Patients with active endoscopic disease were included. Two cohorts were examined: TDM-based decision to escalate (TDM) and clinical decision (non-TDM). Outcomes recorded at median 6 months after adjustment included endoscopic remission (Mayo,1, Simple Endoscopic Score for Crohn's Disease,3), C-reactive protein, and inflammatory bowel disease-specific health care utilization. Postadjustment IFX and antibodies to infliximab levels discriminant for endoscopic remission were determined. Multivariable regression evaluated independent predictors of remission. Results: Of note, 312 dose optimizations were examined (149 TDM and 163 non-TDM). Clinically, groups were similar. Sixty-three percent TDM attained postadjustment endoscopic remission compared with 48% non-TDM (P < 0.05). Sixty-nine percentage TDM had significant clinical response (57% non-TDM [P < 0.01]); fewer were hospitalized (22% TDM versus 35% non-TDM, P = 0.025). Patients with ulcerative colitis had shorter time to escalation (10 versus 20 mo, P < 0.0001). Median IFX levels increased after escalation in TDM (1.5 [pre] and 11 mu g/mL [post]; P < 0.0001) and were higher than non-TDM postadjustment levels (11 versus 6.5 mu g/mL, P = 0.015). Postadjustment IFX.4.5 mu g/mL (area under curve = 0.8; 95% confidence interval, 0.71-0.88) and antibodies to infliximab <3.3 U/mL (area under curve = 0.70; 95% confidence interval, 0.63-0.81) were associated with endoscopic remission. Multivariable analysis showed that IFX concentration (odds ratio 1.2 [95% confidence interval, 1.1-1.3]; P < 0.0001) remained an independent predictor of endoscopic remission. Conclusions: TDM before dose adjustment is associated with higher postadjustment levels and endoscopic remission.
引用
收藏
页码:1202 / 1209
页数:8
相关论文
共 35 条
[1]   Association Between Serum Concentration of Infliximab and Efficacy in Adult Patients With Ulcerative Colitis [J].
Adedokun, Omoniyi J. ;
Sandborn, William J. ;
Feagan, Brian G. ;
Rutgeerts, Paul ;
Xu, Zhenhua ;
Marano, Colleen W. ;
Johanns, Jewel ;
Zhou, Honghui ;
Davis, Hugh M. ;
Cornillie, Freddy ;
Reinisch, Walter .
GASTROENTEROLOGY, 2014, 147 (06) :1296-+
[2]   Clinical Utility of Measuring Infliximab and Human Anti-Chimeric Antibody Concentrations in Patients With Inflammatory Bowel Disease [J].
Afif, Waqqas ;
Loftus, Edward V., Jr. ;
Faubion, William A. ;
Kane, Sunanda V. ;
Bruining, David H. ;
Hanson, Karen A. ;
Sandborn, William J. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2010, 105 (05) :1133-1139
[3]   A Panel to Predict Long-term Outcome of Infliximab Therapy for Patients With Ulcerative Colitis [J].
Arias, Maria Theresa ;
Casteele, Niels Vande ;
Vermeire, Severine ;
van Overstraeten, Anthony de Buck ;
Billiet, Thomas ;
Baert, Filip ;
Wolthuis, Albert ;
Van Assche, Gert ;
Noman, Maja ;
Hoffman, Ilse ;
D'Hoore, Andre ;
Gils, Ann ;
Rutgeerts, Paul ;
Ferrante, Marc .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2015, 13 (03) :531-538
[4]   The relationship between infliximab concentrations, antibodies to infliximab and disease activity in Crohn's disease [J].
Casteele, Niels Vande ;
Khanna, Reena ;
Levesque, Barrett G. ;
Stitt, Larry ;
Zou, G. Y. ;
Singh, Sharat ;
Lockton, Steve ;
Hauenstein, Scott ;
Ohrmund, Linda ;
Greenberg, Gordon R. ;
Rutgeerts, Paul J. ;
Gils, Ann ;
Sandborn, William J. ;
Vermeire, Severine ;
Feagan, Brian G. .
GUT, 2015, 64 (10) :1539-1545
[5]   Randomised clinical trial: deep remission in biologic and immunomodulator naive patients with Crohn's disease - a SONIC post hoc analysis [J].
Colombel, J. -F. ;
Reinisch, W. ;
Mantzaris, G. J. ;
Kornbluth, A. ;
Rutgeerts, P. ;
Tang, K. L. ;
Oortwijn, A. ;
Bevelander, G. S. ;
Cornillie, F. J. ;
Sandborn, W. J. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2015, 41 (08) :734-746
[6]   Postinduction serum infliximab trough level and decrease of C-reactive protein level are associated with durable sustained response to infliximab: a retrospective analysis of the ACCENT I trial [J].
Cornillie, Freddy ;
Hanauer, Stephen B. ;
Diamond, Robert H. ;
Wang, Jianping ;
Tang, Kezhen L. ;
Xu, Zhenhua ;
Rutgeerts, Paul ;
Vermeire, Severine .
GUT, 2014, 63 (11) :1721-1727
[7]   Development and validation of a new, simplified endoscopic activity score for Crohn's disease: the SES-CD [J].
Daperno, M ;
D'Haens, G ;
Van Assche, G ;
Baert, F ;
Bulois, P ;
Maunoury, V ;
Sostegni, R ;
Rocca, R ;
Pera, A ;
Gevers, A ;
Mary, JY ;
Colombel, JF ;
Rutgeerts, P .
GASTROINTESTINAL ENDOSCOPY, 2004, 60 (04) :505-512
[8]  
Dumitrescu G, 2015, ALIMENT PHARM THER, V10, P13393
[9]  
Ferrante Marc, 2009, Curr Gastroenterol Rep, V11, P504
[10]   Loss of Response and Requirement of Infliximab Dose Intensification in Crohn's Disease: A Review [J].
Gisbert, Javier P. ;
Panes, Julian .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2009, 104 (03) :760-767