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.

TitleEtanercept, 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.
Publication TypeJournal Article
Year of Publication2009
AuthorsAlousi, AM, Weisdorf, DJ, Logan, BR, Bolaños-Meade, J, Carter, S, DiFronzo, N, Pasquini, M, Goldstein, SC, Ho, VT, Hayes-Lattin, B, Wingard, JR, Horowitz, MM, Levine, JE
Corporate AuthorsBlood and Marrow Transplant Clinical Trials Network
JournalBlood
Volume114
Issue3
Pagination511-7
Date Published2009 Jul 16
ISSN1528-0020
KeywordsAcute Disease, Adolescent, Adrenal Cortex Hormones, Adult, Aged, Anti-Inflammatory Agents, Non-Steroidal, Antineoplastic Agents, Child, Diphtheria Toxin, Drug Therapy, Combination, Etanercept, Graft vs Host Disease, Hematopoietic Stem Cell Transplantation, Humans, Immunoglobulin G, Infections, Interleukin-2, Methylprednisolone, Middle Aged, Mycophenolic Acid, Pentostatin, Receptors, Tumor Necrosis Factor, Recombinant Fusion Proteins, Survival Rate, Treatment Outcome
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.

DOI10.1182/blood-2009-03-212290
Alternate JournalBlood
PubMed ID19443659
PubMed Central IDPMC2713466
Grant ListU10 HL069294 / HL / NHLBI NIH HHS / United States
UG1 HL069286 / HL / NHLBI NIH HHS / United States
U10 HL069290 / HL / NHLBI NIH HHS / United States
U10 HL069301 / HL / NHLBI NIH HHS / United States
U10 HL069330 / HL / NHLBI NIH HHS / United States
U10 HL069249 / HL / NHLBI NIH HHS / United States
U10 HL069348 / HL / NHLBI NIH HHS / United States
U24 CA076518 / CA / NCI NIH HHS / United States
U10 HL069286 / HL / NHLBI NIH HHS / United States