Double unrelated umbilical cord blood vs HLA-haploidentical bone marrow transplantation: the BMT CTN 1101 trial.

TitleDouble unrelated umbilical cord blood vs HLA-haploidentical bone marrow transplantation: the BMT CTN 1101 trial.
Publication TypeJournal Article
Year of Publication2021
AuthorsFuchs, EJ, O'Donnell, PV, Eapen, M, Logan, B, Antin, JH, Dawson, P, Devine, S, Horowitz, MM, Horwitz, ME, Karanes, C, Leifer, E, Magenau, JM, McGuirk, JP, Morris, LE, Rezvani, AR, Jones, RJ, Brunstein, CG
JournalBlood
Volume137
Issue3
Pagination420-428
Date Published2021 01 21
ISSN1528-0020
KeywordsAcute Disease, Adult, Aged, Bone Marrow Transplantation, Cause of Death, Chronic Disease, Female, Fetal Blood, Graft vs Host Disease, Hematopoiesis, HLA Antigens, Humans, Incidence, Male, Middle Aged, Progression-Free Survival, Transplantation, Haploidentical, Treatment Outcome, Unrelated Donors, Young Adult
Abstract

Results of 2 parallel phase 2 trials of transplantation of unrelated umbilical cord blood (UCB) or bone marrow (BM) from HLA-haploidentical relatives provided equipoise for direct comparison of these donor sources. Between June 2012 and June 2018, 368 patients aged 18 to 70 years with chemotherapy-sensitive lymphoma or acute leukemia in remission were randomly assigned to undergo UCB (n = 186) or haploidentical (n = 182) transplant. Reduced-intensity conditioning comprised total-body irradiation with cyclophosphamide and fludarabine for both donor types. Graft-versus-host disease prophylaxis for UCB transplantation was cyclosporine and mycophenolate mofetil (MMF) and for haploidentical transplantation, posttransplant cyclophosphamide, tacrolimus, and MMF. The primary end point was 2-year progression-free survival (PFS). Treatment groups had similar age, sex, self-reported ethnic origin, performance status, disease, and disease status at randomization. Two-year PFS was 35% (95% confidence interval [CI], 28% to 42%) compared with 41% (95% CI, 34% to 48%) after UCB and haploidentical transplants, respectively (P = .41). Prespecified analysis of secondary end points recorded higher 2-year nonrelapse mortality after UCB, 18% (95% CI, 13% to 24%), compared with haploidentical transplantation, 11% (95% CI, 6% to 16%), P = .04. This led to lower 2-year overall survival (OS) after UCB compared with haploidentical transplantation, 46% (95% CI, 38-53) and 57% (95% CI 49% to 64%), respectively (P = .04). The trial did not demonstrate a statistically significant difference in the primary end point, 2-year PFS, between the donor sources. Although both donor sources extend access to reduced-intensity transplantation, analyses of secondary end points, including OS, favor haploidentical BM donors. This trial was registered at www.clinicaltrials.gov as #NCT01597778.

DOI10.1182/blood.2020007535
Alternate JournalBlood
PubMed ID33475736
PubMed Central IDPMC7819761
Grant ListU10 HL069294 / HL / NHLBI NIH HHS / United States
UG1 HL069290 / HL / NHLBI NIH HHS / United States
UG1 HL069249 / HL / NHLBI NIH HHS / United States
U24 HL138660 / HL / NHLBI NIH HHS / United States
UG1 HL069310 / HL / NHLBI NIH HHS / United States
U10 HL069310 / HL / NHLBI NIH HHS / United States
UG1 HL069274 / HL / NHLBI NIH HHS / United States