Department of Gastroenterology, Icahn School of Medicine, Mount Sinai Medical Center, New York, New York.
Janssen Research & Development, Spring House, Pennsylvania.
Clin Gastroenterol Hepatol. 2019 Jul;17(8):1525-1532.e1. doi: 10.1016/j.cgh.2018.09.033. Epub 2018 Sep 26.
BACKGROUND & AIMS: Among immunosuppressive- and biologic-naïve patients with moderately-to-severely active Crohn's disease (CD), a higher proportion of those treated with the combination of infliximab and azathioprine achieved corticosteroid-free remission at week 26 (CSFR26) than those given infliximab monotherapy; patients given the combination therapy also had higher serum concentrations of infliximab. Enhanced benefit of combination therapy may occur through synergistic modes of action or the influence of azathioprine on infliximab pharmacokinetics.
We analyzed data from 206 patients from whom week 30 serum samples were available: 97 received infliximab monotherapy (5 mg/kg, n = 97) and 109 received combination therapy (2.5 mg/kg/day; n = 109). Proportions of patients achieving CSFR26 and mucosal healing (absence of ulcers) at week 26 were calculated for each quartile of serum concentrations of infliximab, and exposure-response relationships were compared.
Within quartiles of serum concentrations of infliximab, CSFR26 did not differ significantly between patients who received combination therapy vs monotherapy. However, among patients in the lowest quartile of serum concentration of infliximab, twice as many patients who received infliximab monotherapy achieved CSFR26 vs combination therapy. Anti-drug antibodies were detected only in the lowest quartile of serum concentrations of infliximab-in 35.9% of patients given monotherapy and 8.3% of patients given combination therapy.
Among patients with CD and similar serum concentrations of infliximab, combination therapy with azathioprine was not significantly more effective than infliximab monotherapy. Combination therapy with azathioprine appears to improve efficacy by increasing pharmacokinetic features of infliximab. ClinicalTrials.gov, NCT00094458.
在接受免疫抑制和生物制剂治疗的中度至重度活动期克罗恩病(CD)患者中,与接受英夫利昔单抗单药治疗的患者相比,接受英夫利昔单抗联合硫唑嘌呤治疗的患者在第 26 周(CSFR26)达到无皮质激素缓解的比例更高;接受联合治疗的患者英夫利昔单抗的血清浓度也更高。联合治疗的增强益处可能是通过协同作用模式或硫唑嘌呤对英夫利昔单抗药代动力学的影响而产生的。
我们分析了来自 206 名患者的第 30 周血清样本数据:97 名患者接受英夫利昔单抗单药治疗(5mg/kg,n=97),109 名患者接受联合治疗(2.5mg/kg/天;n=109)。计算了每个英夫利昔单抗血清浓度四分位数中达到第 26 周 CSFR26 和黏膜愈合(无溃疡)的患者比例,并比较了暴露-反应关系。
在英夫利昔单抗血清浓度四分位数内,联合治疗与单药治疗的患者在 CSFR26 方面没有显著差异。然而,在英夫利昔单抗血清浓度最低四分位数的患者中,接受英夫利昔单抗单药治疗的患者达到 CSFR26 的比例是接受联合治疗的两倍。仅在英夫利昔单抗血清浓度最低四分位数中检测到抗药物抗体,在接受单药治疗的患者中占 35.9%,在接受联合治疗的患者中占 8.3%。
在 CD 患者中,与英夫利昔单抗单药治疗相比,联合使用硫唑嘌呤治疗并没有显著提高疗效。硫唑嘌呤联合治疗似乎通过增加英夫利昔单抗的药代动力学特征来提高疗效。ClinicalTrials.gov,NCT00094458。