Improved outcomes of UM171–expanded cord blood transplantation compared with other graft sources: real-world evidence

Author:

Cohen Sandra12,Bambace Nadia12,Ahmad Imran12ORCID,Roy Jean12,Tang Xiaoying3,Zhang Mei-Jie3,Burns Linda3,Barabé Frédéric4,Bernard Léa12,Delisle Jean-Sébastien12ORCID,Kiss Thomas12,Lachance Silvy12,Roy Denis-Claude12,Veilleux Olivier12,Sauvageau Guy125

Affiliation:

1. 1Institut Universitaire d'Hémato-Oncologie et de Thérapie Cellulaire, Hôpital Maisonneuve-Rosemont, CIUSSS de l’Est de l’Île de Montréal, Montréal, QC, Canada

2. 2Department of Medicine, Faculty of Medicine, Université de Montréal, Montréal, QC, Canada

3. 3Center for International Blood and Marrow Transplant Research, Milwaukee, WI

4. 4Centre Hospitalier Universitaire de Québec, Université Laval, Québec, QC, Canada

5. 5Institut de Recherche en Immunologie et Cancérologie, Université de Montréal, Montréal, QC, Canada

Abstract

Abstract Cord blood (CB) transplantation is hampered by low cell dose and high nonrelapse mortality (NRM). A phase 1-2 trial of UM171-expanded CB transplants demonstrated safety and favorable preliminary efficacy. The aim of the current analysis was to retrospectively compare results of the phase 1-2 trial with those after unmanipulated CB and matched-unrelated donor (MUD) transplants. Data from recipients of CB and MUD transplants were obtained from the Center for International Blood and Marrow Transplant Research (CIBMTR) database. Patients were directly matched for the number of previous allogeneic hematopoietic stem cell transplants (alloHCT), disease and refined Disease Risk Index. Patients were further matched by propensity score for age, comorbidity index, and performance status. Primary end points included NRM, progression-free survival (PFS), overall survival (OS), and graft-versus-host disease (GVHD)-free relapse-free survival (GRFS) at 1 and 2 years after alloHCT. Overall, 137 patients from CIBMTR (67 CB, 70 MUD) and 22 with UM171-expanded CB were included. NRM at 1 and 2 years was lower, PFS and GRFS at 2 years and OS at 1 year were improved for UM171-expanded CBs compared with CB controls. Compared with MUD controls, UM171 recipients had lower 1- and 2-year NRM, higher 2-year PFS, and higher 1- and 2-year GRFS. Furthermore, UM171-expanded CB recipients experienced less grades 3-4 acute GVHD and chronic GVHD compared with MUD graft recipients. Compared with real-world evidence with CB and MUD alloHCT, this study suggests that UM171-expanded CB recipients may benefit from lower NRM and higher GRFS. This trial was registered at www.clinicaltrials.gov as #NCT02668315.

Publisher

American Society of Hematology

Subject

Hematology

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