首页> 外文期刊>The Lancet >Early combined immunosuppression or conventional management in patients with newly diagnosed Crohn's disease: an open randomised trial.
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Early combined immunosuppression or conventional management in patients with newly diagnosed Crohn's disease: an open randomised trial.

机译:新诊断的克罗恩病患者的早期联合免疫抑制或常规治疗:一项开放随机试验。

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BACKGROUND: Most patients who have active Crohn's disease are treated initially with corticosteroids. Although this approach usually controls symptoms, many patients become resistant to or dependent on corticosteroids, and long exposure is associated with an increased risk of mortality. We aimed to compare the effectiveness of early use of combined immunosuppression with conventional management in patients with active Crohn's disease who had not previously received glucocorticoids, antimetabolites, or infliximab. METHODS: We did a 2-year open-label randomised trial at 18 centres in Belgium, Holland, and Germany between May, 2001, and January, 2004. We randomly assigned 133 patients to either early combined immunosuppression or conventional treatment. The 67 patients assigned to combined immunosuppression received three infusions of infliximab (5 mg/kg of bodyweight) at weeks 0, 2, and 6, with azathioprine. We gave additional treatment with infliximab and, if necessary, corticosteroids, to control disease activity. 66 patients assigned to conventional management received corticosteroids, followed, in sequence, by azathioprine and infliximab. The primary outcome measures were remission without corticosteroids and without bowel resection at weeks 26 and 52. Analysis was by modified intention to treat. This trial was registered with ClinicalTrials.gov, number NCT00554710. FINDINGS: Four patients (two in each group) did not receive treatment as per protocol. At week 26, 39 (60.0%) of 65 patients in the combined immunosuppression group were in remission without corticosteroids and without surgical resection, compared with 23 (35.9%) of 64 controls, for an absolute difference of 24.1% (95% CI 7.3-40.8, p=0.0062). Corresponding rates at week 52 were 40/65 (61.5%) and 27/64 (42.2%) (absolute difference 19.3%, 95% CI 2.4-36.3, p=0.0278). 20 of the 65 patients (30.8%) in the early combined immunosuppression group had serious adverse events, compared with 19 of 64 (25.3%) controls (p=1.0). INTERPRETATION: Combined immunosuppression was more effective than conventional management for induction of remission and reduction of corticosteroid use in patients who had been recently diagnosed with Crohn's disease. Initiation of more intensive treatment early in the course of the disease could result in better outcomes.
机译:背景:大多数患有活动性克罗恩病的患者最初都使用皮质类固醇治疗。尽管这种方法通常可以控制症状,但许多患者对皮质类固醇耐药或依赖皮质类固醇,长时间接触会增加死亡风险。我们旨在比较早期未曾接受糖皮质激素,抗代谢物或英夫利昔单抗的活动性克罗恩病患者早期使用联合免疫抑制与常规治疗的有效性。方法:我们在2001年5月至2004年1月之间在比利时,荷兰和德国的18个中心进行了为期2年的开放标签随机试验。我们随机分配133例患者进行早期联合免疫抑制或常规治疗。分配了联合免疫抑制作用的67名患者在第0、2和6周接受了3次英夫利昔单抗(5 mg / kg体重)输注硫唑嘌呤。我们给予了英夫利昔单抗和必要时使用皮质类固醇的其他治疗,以控制疾病的活动。接受常规治疗的66名患者接受了皮质类固醇治疗,依次接受硫唑嘌呤和英夫利昔单抗治疗。主要的结局指标是在第26和52周时无糖皮质激素和无肠切除的缓解。该试验已在ClinicalTrials.gov上注册,编号为NCT00554710。结果:4名患者(每组2名)未按方案接受治疗。在第26周时,联合免疫抑制组的65例患者中有39例(60.0%)在没有皮质类固醇且未进行手术切除的情况下获得了缓解,而64例对照组中有23例(35.9%)有所缓解,绝对差值为24.1%(95%CI 7.3) -40.8,p = 0.0062)。第52周的相应比率为40/65(61.5%)和27/64(42.2%)(绝对差异19.3%,95%CI 2.4-36.3,p = 0.0278)。早期联合免疫抑制组65例患者中有20例(30.8%)出现严重不良事件,而64例对照组中有19例(25.3%)有严重不良事件(p = 1.0)。解释:在最近被诊断为克罗恩病的患者中,联合免疫抑制比常规治疗更有效地诱导缓解和减少皮质类固醇的使用。在病程早期开始更深入的治疗可能会导致更好的结果。

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