Title | Double unrelated umbilical cord blood vs HLA-haploidentical bone marrow transplantation: the BMT CTN 1101 trial. |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Fuchs, 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 |
Journal | Blood |
Volume | 137 |
Issue | 3 |
Pagination | 420-428 |
Date Published | 2021 01 21 |
ISSN | 1528-0020 |
Keywords | Acute 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. |
DOI | 10.1182/blood.2020007535 |
Alternate Journal | Blood |
PubMed ID | 33475736 |
PubMed Central ID | PMC7819761 |
Grant List | U10 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 |