TY - JOUR
T1 - Multicenter Long-Term Follow-Up of Allogeneic Hematopoietic Cell Transplantation with Omidubicel
T2 - A Pooled Analysis of Five Prospective Clinical Trials
AU - Lin, Chenyu
AU - Schwarzbach, Aurelie
AU - Sanz, Jaime
AU - Montesinos, Pau
AU - Stiff, Patrick
AU - Parikh, Suhag
AU - Brunstein, Claudio
AU - Cutler, Corey
AU - Lindemans, Caroline A.
AU - Hanna, Rabi
AU - Koh, Liang Piu
AU - Jagasia, Madan H.
AU - Valcarcel, David
AU - Maziarz, Richard T.
AU - Keating, Amy K.
AU - Hwang, William Y.K.
AU - Rezvani, Andrew R.
AU - Karras, Nicole A.
AU - Fernandes, Juliana F.
AU - Rocha, Vanderson
AU - Badell, Isabel
AU - Ram, Ron
AU - Schiller, Gary J.
AU - Volodin, Leonid
AU - Walters, Mark C.
AU - Hamerschlak, Nelson
AU - Cilloni, Daniela
AU - Frankfurt, Olga
AU - McGuirk, Joseph P.
AU - Kurtzberg, Joanne
AU - Sanz, Guillermo
AU - Simantov, Ronit
AU - Horwitz, Mitchell E.
N1 - Publisher Copyright:
© 2023 The American Society for Transplantation and Cellular Therapy
PY - 2023/5
Y1 - 2023/5
N2 - Omidubicel is an umbilical cord blood (UCB)-derived ex vivo-expanded cellular therapy product that has demonstrated faster engraftment and fewer infections compared with unmanipulated UCB in allogeneic hematopoietic cell transplantation. Although the early benefits of omidubicel have been established, long-term outcomes remain unknown. We report on a planned pooled analysis of 5 multicenter clinical trials including 105 patients with hematologic malignancies or sickle cell hemoglobinopathy who underwent omidubicel transplantation at 26 academic transplantation centers worldwide. With a median follow-up of 22 months (range, .3 to 122 months), the 3-year estimated overall survival and disease-free survival were 62.5% and 54.0%, respectively. With up to 10 years of follow-up, omidubicel showed durable trilineage hematopoiesis. Serial quantitative assessments of CD3+, CD4+, CD8+, CD19+, CD116+CD56+, and CD123+ immune subsets revealed median counts remaining within normal ranges through up to 8 years of follow-up. Secondary graft failure occurred in 5 patients (5%) in the first year, with no late cases reported. One case of donor-derived myeloid neoplasm was reported at 40 months post-transplantation. This was also observed in a control arm patient who received only unmanipulated UCB. Overall, omidubicel demonstrated stable trilineage hematopoiesis, immune competence, and graft durability in extended follow-up.
AB - Omidubicel is an umbilical cord blood (UCB)-derived ex vivo-expanded cellular therapy product that has demonstrated faster engraftment and fewer infections compared with unmanipulated UCB in allogeneic hematopoietic cell transplantation. Although the early benefits of omidubicel have been established, long-term outcomes remain unknown. We report on a planned pooled analysis of 5 multicenter clinical trials including 105 patients with hematologic malignancies or sickle cell hemoglobinopathy who underwent omidubicel transplantation at 26 academic transplantation centers worldwide. With a median follow-up of 22 months (range, .3 to 122 months), the 3-year estimated overall survival and disease-free survival were 62.5% and 54.0%, respectively. With up to 10 years of follow-up, omidubicel showed durable trilineage hematopoiesis. Serial quantitative assessments of CD3+, CD4+, CD8+, CD19+, CD116+CD56+, and CD123+ immune subsets revealed median counts remaining within normal ranges through up to 8 years of follow-up. Secondary graft failure occurred in 5 patients (5%) in the first year, with no late cases reported. One case of donor-derived myeloid neoplasm was reported at 40 months post-transplantation. This was also observed in a control arm patient who received only unmanipulated UCB. Overall, omidubicel demonstrated stable trilineage hematopoiesis, immune competence, and graft durability in extended follow-up.
KW - Allogeneic stem cell transplantation
KW - Clinical trial
KW - Cord blood
KW - Ex vivo expansion
KW - Long-term follow-up
UR - http://www.scopus.com/inward/record.url?scp=85150811876&partnerID=8YFLogxK
U2 - 10.1016/j.jtct.2023.01.031
DO - 10.1016/j.jtct.2023.01.031
M3 - Article
C2 - 36775201
AN - SCOPUS:85150811876
SN - 2666-6367
VL - 29
SP - 338.e1-338.e6
JO - Transplantation and Cellular Therapy
JF - Transplantation and Cellular Therapy
IS - 5
ER -