TY - JOUR
T1 - The correlation between cotransplantation of mesenchymal stem cells and higher recurrence rate in hematologic malignancy patients
T2 - Outcome of a pilot clinical study
AU - Ning, H.
AU - Yang, F.
AU - Jiang, M.
AU - Hu, L.
AU - Feng, K.
AU - Zhang, J.
AU - Yu, Z.
AU - Li, B.
AU - Xu, C.
AU - Li, Y.
AU - Wang, J.
AU - Hu, J.
AU - Lou, X.
AU - Chen, H.
N1 - Funding Information:
We thank Dr Lianming Liao, for reading, commenting and correcting the manuscript. We also thank Professor Liangping Hu for help on statistical analysis. This work was supported by the National 863 Program, Ministry of Science and Technology, People’s Republic of China (No: 2001AA217131).
PY - 2008/3
Y1 - 2008/3
N2 - In this open-label randomized clinical trial, HLA-identical sibling-matched hematopoietic stem cells (HSC) were transplanted (non-MSCs group, n=15) or cotransplanted with mesenchymal stem cells (MSCs) (MSCs group, n=10) in hematologic malignancy patients. The median number of MSCs infused was 3.4 × 105kg-1 (range, 0.3-15.3 × 105kg-1). MSCs infusions were well tolerated. The median time to neutrophil engraftment (absolute neutrophil count >0.5 × 109l-1) was 16 days for MSCs group and 15 days for non-MSCs group. The median time to platelet engraftment (platelet count >50 × 109 l-1) was 30 and 27 days, respectively. Grades II-IV acute graft-versus-host disease (GVHD) was observed respectively, in one (11.1%) and eight (53.3%) evaluable patients. Chronic GVHD was found in one (14.3%) and four (28.6%) evaluable patients. The number of patients who relapsed were six (60.0%) and three (20.0%), and the 3-year disease-free survivals were 30.0 and 66.7%, respectively. Thus cotransplantation of MSCs and HSCs may prevent GVHD, but the relapse rate is obviously higher than the control group. We conclude that use of MSCs must be handled with extreme caution before a large-scale clinical trial is performed.
AB - In this open-label randomized clinical trial, HLA-identical sibling-matched hematopoietic stem cells (HSC) were transplanted (non-MSCs group, n=15) or cotransplanted with mesenchymal stem cells (MSCs) (MSCs group, n=10) in hematologic malignancy patients. The median number of MSCs infused was 3.4 × 105kg-1 (range, 0.3-15.3 × 105kg-1). MSCs infusions were well tolerated. The median time to neutrophil engraftment (absolute neutrophil count >0.5 × 109l-1) was 16 days for MSCs group and 15 days for non-MSCs group. The median time to platelet engraftment (platelet count >50 × 109 l-1) was 30 and 27 days, respectively. Grades II-IV acute graft-versus-host disease (GVHD) was observed respectively, in one (11.1%) and eight (53.3%) evaluable patients. Chronic GVHD was found in one (14.3%) and four (28.6%) evaluable patients. The number of patients who relapsed were six (60.0%) and three (20.0%), and the 3-year disease-free survivals were 30.0 and 66.7%, respectively. Thus cotransplantation of MSCs and HSCs may prevent GVHD, but the relapse rate is obviously higher than the control group. We conclude that use of MSCs must be handled with extreme caution before a large-scale clinical trial is performed.
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U2 - 10.1038/sj.leu.2405090
DO - 10.1038/sj.leu.2405090
M3 - Article
C2 - 18185520
AN - SCOPUS:40749112327
VL - 22
SP - 593
EP - 599
JO - Leukemia
JF - Leukemia
SN - 0887-6924
IS - 3
ER -