Safety and Efficacy of Granulocyte/Monocyte Apheresis in Steroid-Dependent Active Ulcerative Colitis with Insufficient Response or Intolerance to Immunosuppressants and/or Biologics [the ART Trial]: 12-week Interim Results

被引:33
作者
Dignass, Axel [1 ]
Akbar, Ayesha [2 ,3 ]
Hart, Ailsa [2 ,3 ]
Subramanian, Sreedhar [4 ]
Bommelaer, Gilles [5 ]
Baumgart, Daniel C. [6 ]
Grimaud, Jean-Charles [7 ]
Cadiot, Guillaume [8 ]
Makins, Richard [9 ]
Hoque, Syed [10 ]
Bouguen, Guillaume [11 ,12 ]
Bonaz, Bruno [13 ]
机构
[1] Markus Krankenhaus, Dept Gastroenterol Hepatol Oncol & Metab Dis, Frankfurt, Germany
[2] St Marks Hosp, IBD Unit, London, England
[3] Acad Inst, London, England
[4] Royal Liverpool Univ Hosp, Dept Gastroenterol, Liverpool, Merseyside, England
[5] CHU Clermont Ferrand, Serv Hepatol Gastroenterol, Clermont Ferrand, France
[6] Humboldt Univ, Virchow Hosp, Charite Med Ctr, Dept Med,Div Gastroenterol & Hepatol, Berlin, Germany
[7] Assistance Publ Hop Marseille, Marseille, France
[8] Hop Robert Debre, CHU Reims, Serv Hepatogastroenterol, Reims, France
[9] Cheltenham Gen Hosp, Cheltenham, Glos, England
[10] Whipps Cross Univ Hosp, Barts Hlth NHS Trust, London, England
[11] Univ Hosp Rennes, Serv Malad Appareil Digestif, Pontchaillou, France
[12] Univ Hosp Rennes, CIC1414, Pontchaillou, France
[13] CHU Grenoble, Clin Univ Hepatogastroenterol, Grenoble, France
关键词
Ulcerative colitis; apheresis; adacolumn; INFLAMMATORY-BOWEL-DISEASE; MONOCYTE ADSORPTIVE APHERESIS; EVIDENCE-BASED CONSENSUS; LEUCOCYTAPHERESIS; MANAGEMENT; DIAGNOSIS; ADACOLUMN; THERAPY; DEVICE;
D O I
10.1093/ecco-jcc/jjw032
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background and Aims: Patients with active, steroid-dependent ulcerative colitis with insufficient response or intolerance to immunosuppressants and/or biologic therapies have limited treatment options. Adacolumn, a granulocyte/monocyte adsorptive apheresis device, has shown clinical benefit in these patients. This study aimed to provide additional clinical data regarding the safety and efficacy of Adacolumn in this patient subgroup. Methods: This single-arm, open-label, multicentre trial [ART] was conducted at 18 centres across the UK, France, and Germany. Eligible patients were 18-75 years old with moderate-to-severe, steroid-dependent active ulcerative colitis with insufficient response or intolerance to immunosuppressants and/or biologics. Patients received >= 5 weekly apheresis sessions with Adacolumn. The primary endpoint was clinical remission rate [clinical activity index <= 4] at Week 12. Results: In all, 86 patients were enrolled. At Week 12, 33/84 [39.3%] of patients in the intention-to-treat population achieved clinical remission, with 47/84 [56.0%] achieving a clinical response [clinical activity index reduction of >= 3]. Clinical remission was achieved in 30.0% of patients with previous immunosuppressant and biologic failure; steroid-free clinical remission and response were observed in 22.6% and 35.7% of these patients, respectively. Quality of life [Short Health Scale] significantly improved at Week 12 [p < 0.0001]. The majority of adverse events were of mild/moderate intensity. Conclusions: At Week 12, Adacolumn provided significant clinical benefit in a large cohort of steroid-dependent ulcerative colitis patients with previous failure to immunosuppressant and/or biologic treatment, with a favourable safety profile. These results are consistent with previous studies and support Adacolumn use in this difficult-to-treat patient subgroup.
引用
收藏
页码:812 / 820
页数:9
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