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Volume 15, Issue 12, Pages 1555-1562 (December 2009)


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A Phase III Study of Infliximab and Corticosteroids for the Initial Treatment of Acute Graft-versus-Host Disease

Daniel R. Couriel2Corresponding Author Informationemail address, Rima Saliba1, Marcos de Lima1, Sergio Giralt1, Borje Andersson1, Issa Khouri1, Chitra Hosing1, Cindy Ippoliti3, Elizabeth J. Shpall1, Richard Champlin1, Amin Alousi1

Received 2 July 2009; accepted 2 August 2009. published online 11 September 2009.

Anti-Tumor Necrosis Factor Alpha (TNF-α) therapy with infliximab has shown to be effective for patients with steroid-refractory acute graft-versus-host disease (aGVHD). An open-labeled, phase III trial was conducted to determine if the addition of infliximab to steroids could improve results for patients with newly diagnosed grade II-IV aGVHD. A total of 63 patients were randomized either to 2 mg/kg/day methylprednisolone (MP) or infliximab+ MP. Average age was 47 years (range: 20-70 years); 64% were male. Fifty-three percent and 51% of patients received a matched-sibling and/or bone marrow (BM) graft. Sixty-seven percent had grade II, 33% grade III-IV aGVHD; 62% had skin, 53% gastrointestinal (GI), and 7% had liver involvement. At days 7 and 28, the response rate for infliximab+ MP versus MP was 52% versus 78%, P=.03 and 62% versus 58%, P=.7, respectively. Cumulative incidences of GVHD-related mortality, nonrelapse mortality (NRM), and overall survival (OS) were not significantly different between the 2 groups (GVHD-related mortality: 38% versus 32%, P=.6; NRM: 52% versus 36%, P=.3; OS: 17% and 28%, P=.4 for infliximab+ MP versus MP, respectively). Patients with newly diagnosed aGVHD derive no benefit from the addition of anti-TNF-α therapy with infliximab when compared to corticosteroids alone.

Key WordsAcute GVHD, Infliximab

1 Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas M.D. Anderson Cancer Center, Houston, Texas

2 Sarah Cannon Blood and Marrow Transplantation Program, Tennessee Oncology/Sarah Cannon Research Institute, Nashville, Tennessee

3 Department of Hematology/Oncology, New York Presbiterian Hospital, Cornell Medical Center, New York, New York

Corresponding Author InformationCorrespondence and reprint requests: Daniel R Couriel, MD, 250 25th Avenue North, Suite 412, Nashville, TN 37212.

 Financial disclosure: See Acknowledgments on page 1561.

PII: S1083-8791(09)00365-6

doi:10.1016/j.bbmt.2009.08.003


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