Extracorporeal Photopheresis for the Treatment of Refractory Crohn's Disease: Results of an Open-label Pilot Study

被引:35
作者
Abreu, Maria T. [1 ]
von Tirpitz, Christian [2 ]
Hardi, Robert [3 ]
Kaatz, Martin [4 ]
Van Assche, Gert [5 ]
Rutgeerts, Paul [5 ]
Bisaccia, Emil [6 ]
Goerdt, Sergi [7 ]
Hanauer, Stephen [8 ]
Knobler, Robert [9 ]
Mannon, Peter [10 ]
Mayer, Lloyd [11 ]
Ochsenkuhn, Thomas [12 ]
Sandborn, William J. [13 ]
Parenti, Dennis [14 ]
Lee, Kevin [14 ]
Reinisch, Walter [15 ]
机构
[1] Univ Miami, Miller Sch Med, Miami, FL 33136 USA
[2] Univ Ulm, Dept Digest Dis, Ulm, Germany
[3] Chevy Chase Clin Res, Chevy Chase, MD USA
[4] Univ Jena, Dept Gastroenterol, Jena, Germany
[5] Univ Leuven, Dept Internal Med, Dept Gastroenterol, Louvain, Belgium
[6] Morristown Mem Hosp, Morristown, NJ USA
[7] Univ Mannheim, Dept Gastroenterol, Mannheim, Germany
[8] Univ Chicago, Div Gastroenterol Hepatol & Nutr, Chicago, IL 60637 USA
[9] Univ Vienna, Dept Dermatol, Vienna, Austria
[10] NIAID, Bethesda, MD 20892 USA
[11] Mt Sinai Sch Med, Inst Immunol, New York, NY USA
[12] Univ Munich, Dept Gastroenterol, Munich, Germany
[13] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[14] Therakos Inc, Exton, PA USA
[15] Univ Vienna, Dept Gastroenterol, Vienna, Austria
关键词
extracorporeal photopheresis; 8-methoxypsoralen; anti-TNF therapy; immunomodulators; Crohn's disease; VERSUS-HOST-DISEASE; REGULATORY T-CELLS; CERTOLIZUMAB PEGOL; APOPTOTIC CELLS; LONG-TERM; PHOTOCHEMOTHERAPY; INFLIXIMAB; LYMPHOMA; THERAPY; 6-MERCAPTOPURINE;
D O I
10.1002/ibd.20833
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Extracorporeal photopheresis (ECP) is effective in immune-mediated disorders. A prospective, uncontrolled pilot study was conducted to evaluate the safety and efficacy of ECP in patients with active Crohn's disease (CD) who were refractory to or intolerant of immunosuppressants and/or anti-TNF therapies. Methods: Patients with moderate-to-severely active CD (Crohn's Disease Activity Index [CDAI] 220-450 points) underwent 12 weeks of ECP treatment (Weeks 1-4: twice weekly, every week; Weeks 5-12: twice weekly, every other week). Clinical response was defined as a decrease in the CDAI of : 100 points or remission (CDAI < 150 points) at Week 12. Patients who responded at Week 12 could receive an additional 12 weeks of ECP treatment (twice weekly, every other week) in an extension Study. Results: Twenty-eight patients were enrolled with a mean baseline CDAI score of 314 (range 207-457). At Week 12, 14 patients (50%) responded; 13 patients responded within 6 weeks. Seven patients (25%) attained remission by Week 12. Three of 5 patients with open fistulae at baseline had fistula closure. Response was similar among patients naive to anti-TNF agents and patients who had previously been refractory or intolerant to anti-TNF agents. Of the 12 patients who entered the extension study, 9 (75%) maintained their response at Week 24. Conclusions: In patients with moderate-to-severely active CD who were refractory to or intolerant of immunosuppressants and/or anti-TNF agents, ECP was well tolerated and induced clinical response (50%) and remission (25%) in patients. Most patients were able to maintain a response with Continued treatments.
引用
收藏
页码:829 / 836
页数:8
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