de Ridder Lissy, Rings Edmond H H M, Damen Gerard M, Kneepkens C M Frank, Schweizer Joachim J, Kokke Freddy T M, Benninga Marc A, Norbruis Obbe F, Hoekstra J Hans, Gijsbers Carolien F M, Escher Johanna C
Erasmus Medical Center/Sophia Children's Hospital, Dr. Molewaterplein 60, Rotterdam, Netherlands.
Inflamm Bowel Dis. 2008 Mar;14(3):353-8. doi: 10.1002/ibd.20329.
Infliximab is effective for induction and maintenance of remission in Crohn's disease. It is unknown how long patients should be kept on infliximab therapy. The primary aim of this study was to assess duration of effective maintenance therapy and infliximab dependency in pediatric CD patients initially responding to infliximab therapy.
All pediatric patients treated with infliximab by pediatric gastroenterologists in the Netherlands because of severe luminal or fistulizing CD with initial response to infliximab therapy were reviewed. Duration of therapy, clinical response and adverse events were recorded.
Sixty-six CD patients (37 boys) in 10 hospitals were initially responding to infliximab therapy. Mean age at the start of infliximab therapy was 14.5 years (range, 8.1-18.5 years). Mean follow-up since infliximab was started was 41.3 months (range 12-165). In total, 991 infusions were administered. Analysis demonstrates that 15.2% of patients had prolonged response, while 56.1% were infliximab dependent and 28.8% lost response. In total, 10 patients (15.2%) developed an infection during infliximab therapy and 8 (12.1%) had an immediate allergic reaction.
Good clinical response to maintenance infliximab therapy was seen in 70% of patients. Infliximab maintenance therapy seems very effective and safe in pediatric CD. However, more than half of the patients in this cohort is dependent on repeated infliximab infusions. The number of infliximab infusions received when patients lost response to infliximab was diverse. There was no statistical difference regarding response to infliximab therapy when started early as compared to later in the course of Crohn's disease.
英夫利昔单抗对克罗恩病的诱导缓解和维持缓解有效。目前尚不清楚患者应接受英夫利昔单抗治疗多长时间。本研究的主要目的是评估最初对英夫利昔单抗治疗有反应的儿童克罗恩病患者有效维持治疗的持续时间和对英夫利昔单抗的依赖性。
回顾了荷兰儿科胃肠病学家因严重肠腔型或瘘管型克罗恩病且最初对英夫利昔单抗治疗有反应而接受英夫利昔单抗治疗的所有儿科患者。记录治疗持续时间、临床反应和不良事件。
10家医院的66例克罗恩病患者(37名男孩)最初对英夫利昔单抗治疗有反应。英夫利昔单抗治疗开始时的平均年龄为14.5岁(范围8.1 - 18.5岁)。自开始使用英夫利昔单抗以来的平均随访时间为41.3个月(范围12 - 165个月)。共进行了991次输注。分析表明,15.2%的患者有延长反应,56.1%对英夫利昔单抗有依赖性,28.8%失去反应。英夫利昔单抗治疗期间共有10名患者(15.2%)发生感染,8名患者(12.1%)出现即刻过敏反应。
70%的患者对英夫利昔单抗维持治疗有良好的临床反应。英夫利昔单抗维持治疗在儿童克罗恩病中似乎非常有效且安全。然而,该队列中超过一半的患者依赖重复输注英夫利昔单抗。患者对英夫利昔单抗失去反应时接受的输注次数各不相同。在克罗恩病病程早期开始使用英夫利昔单抗治疗与后期开始治疗相比,对英夫利昔单抗治疗的反应无统计学差异。