Gastroenterology. 2014 Feb;146(2):392-400.e3. doi: 10.1053/j.gastro.2013.10.052.
BACKGROUND & AIMS: The comparative efficacy and safety of infliximab and azathioprine therapy alone or in combination for ulcerative colitis (UC) have not been evaluated previously.
This randomized, double-blind trial evaluated the efficacy and safety of 16 weeks of treatment with infliximab monotherapy, azathioprine monotherapy, or the 2 drugs combined in tumor necrosis factor-a antagonist-naive adults with moderate to severe UC. Patients were assigned randomly to receive intravenous infusions of infliximab 5 mg/kg at weeks 0, 2, 6, and 14 plus daily oral placebo capsules; oral azathioprine 2.5 mg/kg daily plus placebo infusions on the infliximab schedule; or combination therapy with the 2 drugs. Corticosteroid-free clinical remission (primary end point, week 16) was evaluated at weeks 8 and 16. The study was terminated before the enrollment target was reached.
A total of 239 patients were included in efficacy analyses. Baseline characteristics were similar between treatment groups. Corticosteroid-free remission at week 16 was achieved by 39.7% (31 of 78) of patients receiving infliximab/azathioprine,compared with 22.1% (17 of 77) receiving infliximab alone(P =.017) and 23.7% (18 of 76) receiving azathioprine alone(P =.032). Mucosal healing at week 16 occurred in 62.8% (49 of 78) of patients receiving infliximab/azathioprine, compared with 54.6% (42 of 77) receiving infliximab (P = .295) and 36.8% (28 of 76) receiving azathioprine (P =.001). Serious infections occurred in 2 patients (1 patient receiving infliximab,and 1 patient receiving azathioprine).
Anti–tumor necrosis factor-a–naive patients with moderate to severe UC treated with infliximab plus azathioprine were more likely to achieve corticosteroid-free remission at 16 weeks than those receiving either monotherapy. Combination therapy led to significantly better mucosal healing than azathioprine monotherapy. ClinicalTrials.gov number, NCT00537316.
尚未评估英夫利昔单抗和硫唑嘌呤单独或联合治疗溃疡性结肠炎(UC)的疗效和安全性。
本随机、双盲试验评估了肿瘤坏死因子-α拮抗剂初治的中重度 UC 成年患者接受英夫利昔单抗单药治疗、硫唑嘌呤单药治疗或两种药物联合治疗 16 周的疗效和安全性。患者被随机分配接受静脉注射英夫利昔单抗 5mg/kg,分别在第 0、2、6 和 14 周,以及每日口服安慰剂胶囊;每天口服硫唑嘌呤 2.5mg/kg,同时在英夫利昔单抗给药方案中给予安慰剂输注;或联合两种药物治疗。主要终点为第 16 周时无皮质类固醇的临床缓解。在第 8 周和第 16 周评估研究。在达到入组目标之前,研究提前终止。
共纳入 239 例患者进行疗效分析。治疗组之间的基线特征相似。第 16 周时无皮质类固醇缓解的患者分别为英夫利昔单抗/硫唑嘌呤组 39.7%(78 例中的 31 例),英夫利昔单抗组 22.1%(77 例中的 17 例)(P =.017),硫唑嘌呤组 23.7%(76 例中的 18 例)(P =.032)。第 16 周时黏膜愈合的患者分别为英夫利昔单抗/硫唑嘌呤组 62.8%(78 例中的 49 例),英夫利昔单抗组 54.6%(77 例中的 42 例)(P =.295),硫唑嘌呤组 36.8%(76 例中的 28 例)(P =.001)。有 2 例患者(1 例接受英夫利昔单抗,1 例接受硫唑嘌呤)发生严重感染。
与接受英夫利昔单抗单药治疗的患者相比,初治中重度 UC 患者接受英夫利昔单抗联合硫唑嘌呤治疗在 16 周时更有可能达到无皮质类固醇缓解。联合治疗与硫唑嘌呤单药治疗相比,黏膜愈合显著改善。临床试验注册号,NCT00537316。