Etanercept, mycophenolate, denileukin, or pentostatin plus corticosteroids for acute graft-versus-host disease: a randomized phase 2 trial from the Blood and Marrow Transplant Clinical Trials Network

Author:

Alousi Amin M.1,Weisdorf Daniel J.2,Logan Brent R.3,Bolaños-Meade Javier4,Carter Shelly5,DiFronzo Nancy6,Pasquini Marcelo7,Goldstein Steven C.8,Ho Vincent T.9,Hayes-Lattin Brandon10,Wingard John R.11,Horowitz Mary M.12,Levine John E.13

Affiliation:

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

2. Department of Bone Marrow Transplantation, University of Minnesota, Minneapolis;

3. Department of Population Health, Medical College of Wisconsin, Milwaukee;

4. Department of Oncology, The Johns Hopkins University, Baltimore, MD;

5. The EMMES Corporation, Rockville, MD;

6. Transfusion Medicine and Cellular Therapeutics Branch, National Heart, Lung, and Blood Institute, National Institutes of Health/Department of Health and Human Services, Bethesda, MD;

7. Division of Neoplastic Diseases and Related Disorders, Department of Medicine, Center for International Blood and Marrow Transplant Research (CIBMTR) Medical College of Wisconsin, Milwaukee;

8. Division of Hematology/Oncology, University of Pennsylvania, Philadelphia;

9. Department of Medical Oncology/Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, MA;

10. School of Medicine, Oregon Health and Science University, Portland;

11. Department of Medicine, University of Florida Shands Cancer Center, Gainesville;

12. Division of Neoplastic Diseases and Related Disorders, Department of Medicine, and CIBMTR, Froedtert and The Medical College of Wisconsin, Milwaukee; and

13. Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor

Abstract

Abstract Acute graft-versus-host disease (aGVHD) is the primary limitation of allogeneic hematopoietic cell transplantation. Corticosteroids remain the standard initial therapy, yet only 25% to 41% of patients completely respond. This randomized, 4-arm, phase 2 trial was designed to identify the most promising agent(s) for initial therapy for aGVHD. Patients were randomized to receive methylprednisolone 2 mg/kg per day plus etanercept, mycophenolate mofetil (MMF), denileukin diftitox (denileukin), or pentostatin. Patients (n = 180) were randomized; their median age was 50 years (range, 7.5-70 years). Myeloablative conditioning represented 66% of transplants. Grafts were peripheral blood (61%), bone marrow (25%), or umbilical cord blood (14%); 53% were from unrelated donors. Patients who received MMF for prophylaxis (24%) were randomized to a non-MMF arm. At randomization, aGVHD was grade I to II (68%), III to IV (32%), and (53%) had visceral organ involvement. Day 28 complete response rates were etanercept 26%, MMF 60%, denileukin 53%, and pentostatin 38%. Corresponding 9-month overall survival was 47%, 64%, 49%, and 47%, respectively. Cumulative incidences of severe infections were as follows: etanercept 48%, MMF 44%, denileukin 62%, and pentostatin 57%. Efficacy and toxicity data suggest the use of MMF plus corticosteroids is the most promising regimen to compare against corticosteroids alone in a definitive phase 3 trial. This study is registered at http://www.clinicaltrials.gov as NCT00224874.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference24 articles.

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