Crohn's disease management after intestinal resection: a randomised trial

被引:482
作者
De Cruz, Peter [1 ,5 ]
Kamm, Michael A. [1 ,4 ]
Hamilton, Amy L. [1 ]
Ritchie, Kathryn J. [1 ]
Krejany, Efrosinia O. [1 ]
Gorelik, Alexandra [6 ,7 ]
Liew, Danny [6 ,7 ]
Prideaux, Lani [1 ]
Lawrance, Ian C. [8 ,9 ]
Andrews, Jane M. [10 ,11 ]
Bampton, Peter A. [12 ,13 ]
Gibson, Peter R. [14 ,15 ]
Sparrow, Miles [14 ]
Leong, Rupert W. [16 ,17 ,18 ,19 ,20 ]
Florin, Timothy H. [21 ]
Gearry, Richard B. [22 ]
Radford-Smith, Graham [23 ]
Macrae, Finlay A. [24 ,25 ,26 ]
Debinski, Henry [27 ]
Selby, Warwick [28 ]
Kronborg, Ian [29 ]
Johnston, Michael J. [2 ,3 ]
Woods, Rodney [2 ,3 ]
Elliott, P. Ross [1 ]
Bell, Sally J. [1 ]
Brown, Steven J. [1 ]
Connell, William R. [1 ]
Desmond, Paul V. [1 ]
机构
[1] St Vincents Hosp, Dept Gastroenterol, Melbourne, Vic 3065, Australia
[2] St Vincents Hosp, Dept Colorectal Surg, Melbourne, Vic 3065, Australia
[3] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[4] Univ London Imperial Coll Sci Technol & Med, Dept Med, London, England
[5] Univ Melbourne, Austin Hlth, Austin Acad Ctr, Heidelberg, Vic, Australia
[6] Univ Melbourne, Melbourne EpiCtr, Melbourne, Vic, Australia
[7] Melbourne Hlth, Melbourne, Vic, Australia
[8] Fremantle Hosp, Ctr Infl ammatory Bowel Dis, Fremantle, WA, Australia
[9] Univ Western Australia, Fremantle, WA, Australia
[10] Royal Adelaide Hosp, Dept Gastroenterol & Hepatol, Adelaide, SA 5000, Australia
[11] Univ Adelaide, Adelaide, SA, Australia
[12] Flinders Med Ctr, Dept Gastroenterol & Hepatol, Adelaide, SA, Australia
[13] Flinders Univ S Australia, Adelaide, SA 5001, Australia
[14] Alfred Hlth, Dept Gastroenterol, Melbourne, Vic, Australia
[15] Monash Univ, Melbourne, Vic 3004, Australia
[16] Concord Hosp, Gastroenterol Serv, Sydney, NSW, Australia
[17] Concord Hosp, Liver Serv, Sydney, NSW, Australia
[18] Bankstown Hosp, Gastroenterol Serv, Sydney, NSW, Australia
[19] Bankstown Hosp, Liver Serv, Sydney, NSW, Australia
[20] Univ New S Wales, Sydney, NSW, Australia
[21] Univ Queensland, Dept Gastroenterol, Mater Hlth Serv, Brisbane, Qld, Australia
[22] Univ Otago, Dept Med, Christchurch, New Zealand
[23] Univ Queensland, QIMR Berghofer Med Res Inst, Sch Med, Ammatory Bowel Dis Unit,Royal Brisbane & Womens H, Brisbane, Qld, Australia
[24] Royal Melbourne Hosp, Dept Colorectal Med & Genet, Melbourne, Vic, Australia
[25] Royal Melbourne Hosp, Dept Med, Melbourne, Vic, Australia
[26] Univ Melbourne, Melbourne, Vic, Australia
[27] Cabrini Hosp, Melbourne Gastrointestinal Invest Unit, Melbourne, Vic, Australia
[28] Royal Prince Alfred Hosp, AW Morrow Gastroenterol & Liver Ctr, Sydney, NSW, Australia
[29] Western Hosp, Dept Gastroenterol, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
POSTOPERATIVE RECURRENCE; ILEOCOLIC RESECTION; INFLIXIMAB; ADALIMUMAB; PREVENTION; THERAPY; SURGERY; AZATHIOPRINE; MAINTENANCE; RISK;
D O I
10.1016/S0140-6736(14)61908-5
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Most patients with Crohn's disease need an intestinal resection, but a majority will subsequently experience disease recurrence and require further surgery. This study aimed to identify the optimal strategy to prevent postoperative disease recurrence. Methods In this randomised trial, consecutive patients from 17 centres in Australia and New Zealand undergoing intestinal resection of all macroscopic Crohn's disease, with an endoscopically accessible anastomosis, received 3 months of metronidazole therapy. Patients at high risk of recurrence also received a thiopurine, or adalimumab if they were intolerant to thiopurines. Patients were randomly assigned to parallel groups: colonoscopy at 6 months (active care) or no colonoscopy (standard care). We used computer-generated block randomisation to allocate patients in each centre to active or standard care in a 2: 1 ratio. For endoscopic recurrence (Rutgeerts score >= i2) at 6 months, patients stepped-up to thiopurine, fortnightly adalimumab with thiopurine, or weekly adalimumab. The primary endpoint was endoscopic recurrence at 18 months. Patients and treating physicians were aware of the patient's study group and treatment, but central reading of the endoscopic findings was undertaken blind to the study group and treatment. Analysis included all patients who received at least one dose of study drug. This trial is registered with ClinicalTrials.gov, number NCT00989560. Findings Between Oct 13, 2009, and Sept 28, 2011, 174 (83% high risk across both active and standard care groups) patients were enrolled and received at least one dose of study drug. Of 122 patients in the active care group, 47 (39%) stepped-up treatment. At 18 months, endoscopic recurrence occurred in 60 (49%) patients in the active care group and 35 (67%) patients in the standard care group (p=0.03). Complete mucosal normality was maintained in 27 (22%) of 122 patients in the active care group versus four (8%) in the standard care group (p=0.03). In the active care arm, of those with 6 months recurrence who stepped up treatment, 18 (38%) of 47 patients were in remission 12 months later; conversely, of those in remission at 6 months who did not change therapy recurrence occurred in 31 (41%) of 75 patients 12 months later. Smoking (odds ratio [OR] 2.4, 95% CI 1.2-4.8, p=0.02) and the presence of two or more clinical risk factors including smoking (OR 2.8, 95% CI 1.01-7.7, p=0.05) increased the risk of endoscopic recurrence. The incidence and type of adverse and severe adverse events did not differ significantly between patients in the active care and standard care groups (100 [82%] of 122 vs 45 [87%] of 52; p=0.51) and (33 [27%] of 122 vs 18 [35%] of 52; p=0.36), respectively. Interpretation Treatment according to clinical risk of recurrence, with early colonoscopy and treatment step-up for recurrence, is better than conventional drug therapy alone for prevention of postoperative Crohn's disease recurrence. Selective immune suppression, adjusted for early recurrence, rather than routine use, leads to disease control in most patients. Clinical risk factors predict recurrence, but patients at low risk also need monitoring. Early remission does not preclude the need for ongoing monitoring.
引用
收藏
页码:1406 / 1417
页数:12
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