Phase I clinical trial of intra-bone marrow cotransplantation of mesenchymal stem cells in cord blood transplantation
- PMID: 33314650
- PMCID: PMC7980216
- DOI: 10.1002/sctm.20-0381
Phase I clinical trial of intra-bone marrow cotransplantation of mesenchymal stem cells in cord blood transplantation
Abstract
Mesenchymal stem cells (MSCs) have immunomodulatory properties and support hematopoiesis in the bone marrow (BM). To develop a new strategy to not only prevent graft-vs-host disease (GVHD) but also to enhance engraftment, a phase I trial of cord blood transplantation (CBT) combined with intra-BM injection of MSCs (MSC-CBT) was designed. Third-party BM-derived MSCs were injected intra-BM on the day of CBT. The conditioning regimen varied according to patient characteristics. GVHD prophylaxis was tacrolimus and methotrexate. The primary endpoint was toxicity related to intra-BM injection of MSCs. Clinical outcomes were compared with those of six controls who received CBT alone. Five adult patients received MSC-CBT, and no adverse events related to intra-BM injection of MSCs were observed. All patients achieved neutrophil, reticulocyte, and platelet recoveries, with median times to recoveries of 21, 35, and 38 days, respectively, comparable with controls. Grade II-IV acute GVHD developed in three controls but not in MSC-CBT patients. No patients developed chronic GVHD in both groups. At 1 year after transplantation, all MSC-CBT patients survived without relapse. This study shows the safety of MSC-CBT, and the findings also suggest that cotransplantation of MSCs may prevent GVHD with no inhibition of engraftment. This trial was registered at the University Hospital Medical Information Network Clinical Trials Registry as number 000024291.
Keywords: cord blood transplantation; engraftment; graft-vs-host disease; intra-bone marrow; mesenchymal stem cell.
© 2020 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals LLC on behalf of AlphaMed Press.
Conflict of interest statement
T.M. received educational and investigational support from Chugai Pharmaceutical Co., Ltd. and Novo Nordisk Pharma Ltd.; honoraria from Shire/Takeda Pharmaceutical Co., Ltd., Bayer Pharmaceutical Co., Ltd., Bioverativ/Sanofi Co., Ltd., Chugai Pharmaceutical Co., Ltd., CSL Behring Co., Ltd., and Novo Nordisk Pharma Ltd.; serves on advisory boards for Baxalta/Shire/Takeda Pharmaceutical Co., Ltd., Bayer Pharmaceutical Co., Ltd., Novo Nordisk Pharma Ltd., Chugai Pharmaceutical Co., Ltd., and Pfizer Co., Ltd. H.K. received research funding from FUJIFILM Corporation, Kyowa Hakko Kirin Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Perseus Proteomics Inc., Daiichi Sankyo Co., Ltd., AbbVie GK, Astellas Pharma Inc., Zenyaku Kogyo Co., Ltd., Nippon Shinyaku Co., Ltd., Eisai Co., Ltd., Chugai Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., and Sumitomo Dainippon Pharma Co., Ltd.; honoraria from Bristol‐Myers Squibb, Ltd. and Astellas Pharma Inc.; served as the Consultant/Advisory role Astellas, Daiichi Sankyo, received honoraria from Astellas, and received research funding from Chugai, Kyowa Hakko Kirin, Zenyaku Kogyo, FUJIFILM, Daiichi Sankyo, Astellas, Otsuka, Nippon Shinyaku, Eisai, Pfizer, Takeda, Novartis, Sumitomo Dainippon, Sanofi, Celgene. These companies were not directly involved in any part of this study. The other authors indicated no potential conflicts of interest.
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