Brandse Johannan F, Peters Charlotte P, Gecse Krisztina B, Eshuis Emma J, Jansen Jeroen M, Tuynman Hans A, Löwenberg Mark, Ponsioen Cyriel Y, van den Brink Gijs R, DʼHaens Geert R
*Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, The Netherlands; †Department of Gastroenterology and Hepatology, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands; and ‡Department of Gastroenterology and Hepatology, Medisch Centrum Alkmaar, North Holland, The Netherlands.
Inflamm Bowel Dis. 2014 Feb;20(2):251-8. doi: 10.1097/01.MIB.0000438248.14218.1d.
Switches between anti-tumor necrosis factor agents in the treatment of Crohn's disease (CD) occur in case of treatment failure, intolerance, or patient preference. No data are currently available on the usefulness of a second infliximab treatment after earlier discontinuation and previous switch to an alternative anti-tumor necrosis factor agent. In this study, we evaluated the clinical benefit of infliximab retreatment in patients with CD after sequential use of both infliximab and adalimumab.
Twenty-nine patients with CD who had received earlier treatments with sequential infliximab and adalimumab and were then restarted on infliximab were retrieved from a multicenter registry designed for the follow-up of adalimumab treatment for CD. Short-term and sustained effects of infliximab retreatment were evaluated retrospectively by reviewing clinical records. Follow-up was 18 months for all patients.
In 13/29 (45%) patients, infliximab was reintroduced at intensified dosing schedule (>5 mg/kg or <8 wk) for 23/29 (79%) of patients similar to the schedule who were on at time of previous discontinuation. During the second infliximab treatment course, dosing was further intensified in 11 out of 29 (38%) patients. After 18 months 18/29 (62%), patients were still on continued therapy of their second infliximab treatment. Infliximab was discontinued (after a median of 7 mo) in 11 out of 29 patients for loss of response (n = 7 [24%]), intolerance (n = 3 [10%]), or non-compliance (n = 1 [3%]). Use of induction schedule or concomitant immunomodulators were not significantly associated with treatment benefit.
The majority of patients with CD benefit from a second treatment with infliximab after previous treatment with infliximab and adalimumab, which offer a meaningful therapeutic option in often highly refractory patients.
在克罗恩病(CD)治疗中,若出现治疗失败、不耐受或患者偏好等情况,会在抗肿瘤坏死因子药物之间进行转换。目前尚无关于早期停用并先前转换为另一种抗肿瘤坏死因子药物后再次使用英夫利昔单抗治疗的有效性的数据。在本研究中,我们评估了先后使用英夫利昔单抗和阿达木单抗的CD患者再次使用英夫利昔单抗治疗的临床获益。
从一个为阿达木单抗治疗CD随访设计的多中心登记处检索出29例先前先后接受英夫利昔单抗和阿达木单抗治疗、随后重新开始使用英夫利昔单抗的CD患者。通过回顾临床记录对英夫利昔单抗再治疗的短期和持续效果进行回顾性评估。所有患者的随访时间为18个月。
13/29(45%)例患者以强化给药方案(>5mg/kg或<8周)重新使用英夫利昔单抗,23/29(79%)例患者的给药方案与先前停药时相似。在第二次英夫利昔单抗治疗疗程中,29例患者中有11例(38%)进一步强化了给药剂量。18个月后,18/29(62%)例患者仍在继续接受第二次英夫利昔单抗治疗。29例患者中有11例(中位时间7个月)因反应丧失(n = 7 [24%])、不耐受(n = 3 [10%])或不依从(n = 1 [3%])而停用英夫利昔单抗。诱导方案的使用或同时使用免疫调节剂与治疗获益无显著相关性。
大多数先后接受英夫利昔单抗和阿达木单抗治疗的CD患者再次使用英夫利昔单抗治疗有益,这为通常高度难治的患者提供了一种有意义的治疗选择。