A multicenter prospective phase 2 randomized study of extracorporeal photopheresis for treatment of chronic graft-versus-host disease

被引:264
作者
Flowers, Mary E. D. [1 ]
Apperley, Jane F. [2 ]
van Besien, Koen [3 ]
Elmaagacli, Ahmet [4 ]
Grigg, Andrew [5 ]
Reddy, Vijay [6 ]
Bacigalupo, Andrea [7 ]
Kolb, Hans-Jochem [8 ]
Bouzas, Luis [9 ]
Michallet, Mauricette [10 ]
Prince, H. Miles [11 ]
Knobler, Robert [12 ]
Parenti, Dennis [13 ]
Gallo, Jose [13 ]
Greinix, Hildegard T. [14 ]
机构
[1] Univ Washington, Sch Med, Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[2] Univ London Imperial Coll Sci Technol & Med, Royal Hammersmith Hosp, Div Invest Sci, London, England
[3] Univ Chicago, Pritzker Sch Med, Hematol Oncol Sect, Chicago, IL 60637 USA
[4] Univ Klinikum Essen, Klin & Poliklin Knochenmarktranplantat, Essen, Germany
[5] Royal Melbourne Hosp, Clin Haematol & Med Oncol, Parkville, Vic 3050, Australia
[6] Univ Florida, Div Hematol Oncol, Gainesville, FL USA
[7] Osped San Martino Genova, Genoa, Italy
[8] Univ Munich, Munich, Germany
[9] Natl Canc Inst, CEMO, Rio De Janeiro, Brazil
[10] Univ Lyon, Lyon, France
[11] Peter MacCallum Canc Inst, Melbourne, Vic 3000, Australia
[12] Med Univ Vienna, Dept Dermatol, Vienna, Austria
[13] Therakos, Exton, PA USA
[14] Med Univ Vienna, Bone Marrow Transplant Unit, Dept Internal Med 1, Vienna, Austria
关键词
D O I
10.1182/blood-2008-03-141481
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic graft-versus-host disease (cGVHD) is a major limitation of successful hematopoietic cell transplantation. The safety and efficacy of extracorporeal photopheresis (ECP) for 12 to 24 weeks together with standard therapy was compared with standard therapy alone in patients with cutaneous manifestations of cGVHD that could not be adequately controlled by corticosteroid treatment. The primary efficacy end point was a blinded quantitative comparison of percent change from baseline in Total Skin Score (TSS) of 10 body regions at week 12. Ninety- five patients were randomized to either ECP and standard therapy (n = 48) or standard therapy alone (n = 47). The median percentage improvement in TSS at week 12 was 14.5% for the ECP arm and 8.5% for the control arm (P = .48). The proportion of patients who had at least a 50% reduction in steroid dose and at least a 25% decrease from baseline in TSS was 8.3% in the ECP arm at week 12 and 0% in the control arm (P = .04). The nonblinded investigator assessment of skin complete or partial responses revealed a significant improvement in favor of ECP (P < .001). ECP was generally well tolerated. These results suggest that ECP may have a steroid-sparing effect in the treatment of cGVHD. Clinical trials registered at www. Clinical Trials. gov as NCT00054613.
引用
收藏
页码:2667 / 2674
页数:8
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