Ferrante Marc, Papamichael Konstantinos, Duricova Dana, D'Haens Geert, Vermeire Severine, Archavlis Emmanuel, Rutgeerts Paul, Bortlik Martin, Mantzaris Gerassimos, Van Assche Gert
Department of Gastroenterology, University Hospitals Leuven, KU Leuven, Leuven, Belgium
1st Department of Gastroenterology, Evangelismos Hospital, Athens, Greece.
J Crohns Colitis. 2015 Aug;9(8):617-24. doi: 10.1093/ecco-jcc/jjv076. Epub 2015 Apr 29.
Prophylactic azathioprine (AZA) is efficacious in preventing postoperative Crohn's disease (CD) recurrence. However, it is unknown whether AZA should be started immediately after surgery. We compared the efficacy of systematic vs endoscopy-driven AZA in preventing CD recurrence at week 102.
This prospective, multicentre trial included CD patients undergoing curative resection with ileocolonic anastomosis and at higher risk of recurrence. Patients were randomized to systematic AZA initiated ≤2 weeks from surgery, or endoscopy-driven AZA in which therapy was only initiated in case of endoscopic recurrence (Rutgeerts' score ≥i2) at weeks 26 or 52 following surgery. The primary endpoint was endoscopic remission (i0-i1) at week 102. Secondary endpoints included complete endoscopic remission (i0) and clinical remission.
The study was prematurely stopped due to slow recruitment. Between 2005 and 2011, 63 patients (28 male, median age 36 years) were randomized to systematic (n = 32) or endoscopy-driven AZA (n = 31). Twenty-one patients withdrew prematurely (8 clinical recurrence, 6 adverse reactions to AZA, 7 patient's preference). In the endoscopy-driven AZA group, 14 patients had to initiate AZA (11 at week 26, 3 at week 52). Endoscopic remission was achieved by 50% in the systematic and 42% in the endoscopy-driven AZA group (p = 0.521). No difference in secondary endpoints was found.
Systematic AZA therapy in patients at higher risk of postoperative CD recurrence is not superior to endoscopy-driven treatment. Early postoperative endoscopic evaluation between weeks 26 and 52 seems most appropriate to guide further therapy, but larger studies are warranted. (ClinicalTrials.gov NCT02247258.).
预防性使用硫唑嘌呤(AZA)可有效预防克罗恩病(CD)术后复发。然而,AZA是否应在术后立即开始使用尚不清楚。我们比较了系统性使用AZA与内镜引导下使用AZA在第102周预防CD复发的疗效。
这项前瞻性、多中心试验纳入了接受回结肠吻合根治性切除术且复发风险较高的CD患者。患者被随机分为两组,一组在术后≤2周开始系统性使用AZA,另一组为内镜引导下使用AZA,即仅在术后第26周或第52周出现内镜复发( Rutgeerts评分≥i2)时才开始治疗。主要终点是第102周时的内镜缓解(i0-i1)。次要终点包括完全内镜缓解(i0)和临床缓解。
由于入组缓慢,研究提前终止。2005年至2011年期间,63例患者(28例男性,中位年龄36岁)被随机分为系统性使用AZA组(n = 32)或内镜引导下使用AZA组(n = 31)。21例患者提前退出(8例临床复发,6例对AZA有不良反应,7例出于患者个人意愿)。在内镜引导下使用AZA组中,14例患者不得不开始使用AZA(11例在第26周,3例在第52周)。系统性使用AZA组和内镜引导下使用AZA组的内镜缓解率分别为50%和42%(p = 0.521)。次要终点方面未发现差异。
术后CD复发风险较高的患者中,系统性使用AZA治疗并不优于内镜引导下治疗。术后第26周和第52周之间进行早期内镜评估似乎最适合指导进一步治疗,但仍需要更大规模的研究。(ClinicalTrials.gov NCT02247258.)