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
Freddy Cornillie, Stephen B Hanauer, Robert H Diamond, Jianping Wang, Kezhen L Tang, Zhenhua Xu, Paul Rutgeerts, Séverine Vermeire, Freddy Cornillie, Stephen B Hanauer, Robert H Diamond, Jianping Wang, Kezhen L Tang, Zhenhua Xu, Paul Rutgeerts, Séverine Vermeire
Abstract
Background: Serum infliximab trough levels correlate with efficacy; dose escalation is often beneficial in patients with Crohn's disease who stop responding to infliximab treatment.
Objective: To carry out a post hoc analysis of A Crohn's Disease Clinical Trial Evaluating Infliximab in a New Long-term Treatment Regimen I (ACCENT I) to evaluate the association between serum infliximab trough levels and C-reactive protein (CRP) after 14 weeks of induction treatment with durable sustained long-term response (Crohn's Disease Activity Index decrease ≥70 points and reduction ≥25% from baseline).
Design: ACCENT I was a multicentre, randomised, placebo-controlled study. Week 14 trough levels and CRP percentage decrease from baseline to week 14 were compared between patients with and without durable sustained response through week 54. Sensitivity and specificity were determined to predict durable sustained response. Receiver operating characteristic (ROC) curves identified optimal cut-off points; logistic regression determined ORs.
Results: After induction with 5 mg/kg infliximab, 25% (37/147) and 33% (47/144) of patients sustained week 14 response to infliximab 5 or 10 mg/kg, respectively, administered every 8 weeks without dose escalation, through week 54. Median week 14 trough levels of patients with and without durable sustained response to infliximab 5 mg/kg were 4.0 and 1.9 μg/mL, respectively (p=0.0331). Optimal predictors of durable sustained response to maintenance infliximab 5 mg/kg were week 14 trough level ≥3.5 µg/mL and ≥60% CRP decrease (ORs (95% CI), 3.5 (1.1 to 11.4) and 7.3 (1.4 to 36.7)), respectively, in patients with raised baseline CRP (>8.0 mg/L); area under the ROC curve was 0.75 for both predictors. A ≥3.5 µg/mL week 14 infliximab serum level did not predict durable sustained response to 10 mg/kg maintenance infliximab.
Conclusions: Patients with durable sustained response to maintenance infliximab 5 mg/kg had higher postinduction trough levels than patients without durable sustained response. Serum infliximab trough levels ≥3.5 µg/mL and ≥60% CRP decrease were significantly associated with durable sustained response.
Keywords: CROHN'S DISEASE; INFLIXIMAB; PHARMACOKINETICS.
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
Figures




References
- Hanauer SB, Feagan BG, Lichtenstein GR, et al. ; and the ACCENT I Study Group. Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial. Lancet 2002;359:1541–9.
- Ben-Horin S, Chowers Y. Review article: loss of response to anti-TNF treatments in Crohn's disease. Aliment Pharmacol Ther 2011;33:987–95.
- Maser EA, Villela R, Silverberg MS, et al. Association of trough serum infliximab to clinical outcome after scheduled maintenance treatment for Crohn's disease. Clin Gastroenterol Hepatol 2006;4:1248–54.
- Baert F, Noman M, Vermeire S, et al. Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease. N Engl J Med 2003;348:601–8.
- Rutgeerts P, Feagan BG, Lichtenstein GR, et al. Comparison of scheduled and episodic treatment strategies of infliximab in Crohn's disease. Gastroenterology 2004;126:402–13.
- Hanauer SB, Wagner CL, Bala M, et al. Incidence and importance of antibody responses to infliximab after maintenance or episodic treatment in Crohn's disease. Clin Gastroenterol Hepatol 2004;2:542–53.
- Reinisch W, Wang Y, Oddens BJ, et al. C-reactive protein, an indicator for maintained response or remission to infliximab in patients with Crohn's disease: a post-hoc analysis from ACCENT I. Aliment Pharmacol Ther 2012;35:568–76.
- Jürgens M, Mahachie John JM, Cleynen I, et al. Levels of C-reactive protein are associated with response to infliximab therapy in patients with Crohn's disease. Clin Gastroenterol Hepatol 2011;9:421–7 e1.
- Cornillie F, Hanauer SB, Diamond RH, et al. Can clinical, biological or pharmacological markers predict sustained response to infliximab? A retrospective analysis of ACCENT I [abstract]. Gut 2011;60(Suppl 3):A296 United European Gastroenterology Week. Stockholm, Sweden 2011.
- Schnitzler F, Fidder H, Ferrante M, et al. Mucosal healing predicts long-term outcome of maintenance therapy with infliximab in Crohn's disease. Inflamm Bowel Dis 2009;15:1295–301.
- Arias MT, Vande Casteele N, Drobne D, et al. Importance of trough levels and antibodies on the long-term efficacy of infliximab therapy in ulcerative colitis [abstract]. J Crohns Colitis 2012;6(Suppl 1):S5.
- Colombel JF, Sandborn WJ, Reinisch W, et al. ; for the SONIC Study Group. Infliximab, azathioprine, or combination therapy for Crohn's disease. N Engl J Med 2010;362:1383–95.
Source: PubMed
今後の臨床試験
-
Seoul National University HospitalSamil Pharmaceutical Co., Ltd.募集
-
Stanford Universityまだ募集していません急性骨髄性白血病 | 骨髄異形成症候群 | 骨髄増殖性腫瘍アメリカ
-
Cheng Qi募集
-
Stanford Universityまだ募集していません
-
Istanbul Aydın Universityまだ募集していません首の痛み | 筋膜性疼痛症候群 | 仕事関連の筋骨格障害トルコ(Türkiye)
-
Jonsson Comprehensive Cancer CenterStemline Therapeutics, Inc.まだ募集していません再発子宮内膜がん | 進行した子宮内膜がん | 転移性子宮内膜がん | III期の子宮内膜がん | IV期の子宮内膜がんアメリカ
-
University of Colorado, Denver募集思春期特発性脊柱側弯症(AIS) | 神経筋性脊柱側弯症アメリカ
-
University of FloridaAmerican Heart Association募集駆出率が保存された心不全 (HFPEF)アメリカ
-
UNC Lineberger Comprehensive Cancer Centerまだ募集していません白血病 | 急性リンパ芽球性白血病 | リンパ芽球性リンパ腫 | 急性白血病 | 急性リンパ性白血病アメリカ
-
Korea University Anam HospitalThe Catholic University of Korea; Keimyung University Dongsan Medical Center; Medical AI Co., Ltdまだ募集していません泌尿器がん | 非心臓手術後の心筋損傷 | 主要な有害な心血管イベント(MACE)
-
Montefiore Medical Centerまだ募集していませんCesarean Scar Defect (Isthmocele)アメリカ
-
Sanofiまだ募集していません