TY - JOUR
T1 - Feasibility of co-transplantation of umbilical cord blood and third-party mesenchymal stromal cells after (non)myeloablative conditioning in patients with hematological malignancies
AU - Transplant Committee of the Belgian Hematology Society.
AU - Planken, Simon
AU - De Becker, Ann
AU - Kerre, Tessa
AU - Schoemans, Hélène
AU - Baron, Frédéric
AU - Graux, Carlos
AU - Van Riet, Ivan
AU - Lechanteur, Chantal
AU - Baudoux, Etienne
AU - Schots, Rik
AU - Beguin, Yves
N1 - Funding Information:
This work was supported by the Belgian Hematology Society.
Publisher Copyright:
© 2024 Elsevier Masson SAS
PY - 2024/12
Y1 - 2024/12
N2 - Umbilical cord blood (UCB) is an alternative source of stem cells for patients lacking a 9/10 or 10/10 HLA identical donor. However, after UCB transplantation, time to engraftment and immune recovery are prolonged, increasing the risk of fatal complications. Mesenchymal stromal cells (MSC) can support hematopoietic engraftment and have immunosuppressive effects. The primary objective of this phase I/II multicenter study was to determine the feasibility and safety of UCB transplantation with co-infusion of third party MSC, as assessed by treatment related mortality (TRM) at day 100. Secondary objectives were engraftment, immune recovery, occurrence of graft versus host disease (GVHD), infections, disease free survival, relapse incidence and overall survival. Eleven patients were grafted according to this protocol. Allogeneic transplantation after co-infusion appears feasible with 18 % TRM at day 100. Engraftment data show a median time of 16 days to neutrophil and 27 days to platelet recovery, which is shorter than what is usually reported after UCB transplantation. Only 1 episode of acute GVHD was reported. In conclusion, MSC and UCB co-transplantation is feasible and might help overcome some of the drawbacks of UCB transplantation.
AB - Umbilical cord blood (UCB) is an alternative source of stem cells for patients lacking a 9/10 or 10/10 HLA identical donor. However, after UCB transplantation, time to engraftment and immune recovery are prolonged, increasing the risk of fatal complications. Mesenchymal stromal cells (MSC) can support hematopoietic engraftment and have immunosuppressive effects. The primary objective of this phase I/II multicenter study was to determine the feasibility and safety of UCB transplantation with co-infusion of third party MSC, as assessed by treatment related mortality (TRM) at day 100. Secondary objectives were engraftment, immune recovery, occurrence of graft versus host disease (GVHD), infections, disease free survival, relapse incidence and overall survival. Eleven patients were grafted according to this protocol. Allogeneic transplantation after co-infusion appears feasible with 18 % TRM at day 100. Engraftment data show a median time of 16 days to neutrophil and 27 days to platelet recovery, which is shorter than what is usually reported after UCB transplantation. Only 1 episode of acute GVHD was reported. In conclusion, MSC and UCB co-transplantation is feasible and might help overcome some of the drawbacks of UCB transplantation.
KW - Humans
KW - Hematologic Neoplasms/therapy
KW - Mesenchymal Stem Cell Transplantation/methods
KW - Male
KW - Transplantation Conditioning/methods
KW - Female
KW - Middle Aged
KW - Adult
KW - Cord Blood Stem Cell Transplantation/methods
KW - Graft vs Host Disease/prevention & control
KW - Feasibility Studies
KW - Mesenchymal Stem Cells
KW - Young Adult
KW - Aged
KW - Transplantation, Homologous/methods
UR - http://www.scopus.com/inward/record.url?scp=85202540334&partnerID=8YFLogxK
U2 - 10.1016/j.retram.2024.103466
DO - 10.1016/j.retram.2024.103466
M3 - Article
C2 - 39213720
SN - 2452-3186
VL - 72
JO - Current research in translational medicine
JF - Current research in translational medicine
IS - 4
M1 - 103466
ER -