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The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study

BACKGROUND: Bronchiolitis obliterans syndrome (BOS) after allo-HSCT is a devastating complication with limited therapeutic options. We aimed to assess the efficacy and safety of mesenchymal stem cells (MSCs) in BOS after allo-HSCT. METHODS: This multicenter prospective cohort study enrolled 81 allo-...

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Autores principales: Chen, Shan, Zhao, Ke, Lin, Ren, Wang, Shunqing, Fan, Zhiping, Huang, Fen, Chen, Xiaoyong, Nie, Danian, Du, Xin, Guo, Ziwen, Lin, Dongjun, Xuan, Li, Xu, Na, Sun, Jing, Peng Xiang, Andy, Liu, Qifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945279/
https://www.ncbi.nlm.nih.gov/pubmed/31668569
http://dx.doi.org/10.1016/j.ebiom.2019.09.039
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author Chen, Shan
Zhao, Ke
Lin, Ren
Wang, Shunqing
Fan, Zhiping
Huang, Fen
Chen, Xiaoyong
Nie, Danian
Du, Xin
Guo, Ziwen
Lin, Dongjun
Xuan, Li
Xu, Na
Sun, Jing
Peng Xiang, Andy
Liu, Qifa
author_facet Chen, Shan
Zhao, Ke
Lin, Ren
Wang, Shunqing
Fan, Zhiping
Huang, Fen
Chen, Xiaoyong
Nie, Danian
Du, Xin
Guo, Ziwen
Lin, Dongjun
Xuan, Li
Xu, Na
Sun, Jing
Peng Xiang, Andy
Liu, Qifa
author_sort Chen, Shan
collection PubMed
description BACKGROUND: Bronchiolitis obliterans syndrome (BOS) after allo-HSCT is a devastating complication with limited therapeutic options. We aimed to assess the efficacy and safety of mesenchymal stem cells (MSCs) in BOS after allo-HSCT. METHODS: This multicenter prospective cohort study enrolled 81 allo-HSCT recipients whose BOS were diagnosed within 6 months. The choice of prednisone and azithromycin combined with or without MSCs was based on patient preferences (MSC n = 49, non-MSC n = 32). The primary endpoint was response rate at 3 months, defined as the proportion of patients achieving FEV1 improvement or steroid sparing. The trial was registered at ClinicalTrials.gov (NCT02543073). FINDINGS: Response rate was 35/49 patients (71%, 95% CI 59 to 84%) and 14/32 (44%, 27 to 61%) in MSC and non-MSC group, respectively (p = 0.013). The addition of MSCs was associated with a better difference for change in FEV1 rate of decline, compared to non-MSC group (53 mL/months, 2 to 103; p = 0.040). The 3-year overall survival post-diagnosis was 70.6% (55.9 to 85.3%) and 58.2% (36.1 to 78.5%) in MSC and non-MSC group, respectively (p = 0.21). Clinical improvement was accompanied by a significant increase of interleukin (IL)-10-producing CD5+B cells. There was no statistical difference in the rates of infections and leukemia relapse between the two groups. MSCs were well-tolerated with no serious adverse events. INTERPRETATION: MSCs offer an effective and safe therapeutic option for BOS after allo-HSCT. Our study strengthens evidence for clinical use of MSC therapy in BOS. These data also provide novel insight into potential biological mechanisms of MSC treatment and support further investigation in larger randomized controlled trials. FUNDING: National Key R&D Program of China, National Natural Science Foundation of China, Health Collaborative Innovation Major Projects of Guangzhou City, Science and Technology Planning Project of Guangdong Province.
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spelling pubmed-69452792020-01-09 The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study Chen, Shan Zhao, Ke Lin, Ren Wang, Shunqing Fan, Zhiping Huang, Fen Chen, Xiaoyong Nie, Danian Du, Xin Guo, Ziwen Lin, Dongjun Xuan, Li Xu, Na Sun, Jing Peng Xiang, Andy Liu, Qifa EBioMedicine Research paper BACKGROUND: Bronchiolitis obliterans syndrome (BOS) after allo-HSCT is a devastating complication with limited therapeutic options. We aimed to assess the efficacy and safety of mesenchymal stem cells (MSCs) in BOS after allo-HSCT. METHODS: This multicenter prospective cohort study enrolled 81 allo-HSCT recipients whose BOS were diagnosed within 6 months. The choice of prednisone and azithromycin combined with or without MSCs was based on patient preferences (MSC n = 49, non-MSC n = 32). The primary endpoint was response rate at 3 months, defined as the proportion of patients achieving FEV1 improvement or steroid sparing. The trial was registered at ClinicalTrials.gov (NCT02543073). FINDINGS: Response rate was 35/49 patients (71%, 95% CI 59 to 84%) and 14/32 (44%, 27 to 61%) in MSC and non-MSC group, respectively (p = 0.013). The addition of MSCs was associated with a better difference for change in FEV1 rate of decline, compared to non-MSC group (53 mL/months, 2 to 103; p = 0.040). The 3-year overall survival post-diagnosis was 70.6% (55.9 to 85.3%) and 58.2% (36.1 to 78.5%) in MSC and non-MSC group, respectively (p = 0.21). Clinical improvement was accompanied by a significant increase of interleukin (IL)-10-producing CD5+B cells. There was no statistical difference in the rates of infections and leukemia relapse between the two groups. MSCs were well-tolerated with no serious adverse events. INTERPRETATION: MSCs offer an effective and safe therapeutic option for BOS after allo-HSCT. Our study strengthens evidence for clinical use of MSC therapy in BOS. These data also provide novel insight into potential biological mechanisms of MSC treatment and support further investigation in larger randomized controlled trials. FUNDING: National Key R&D Program of China, National Natural Science Foundation of China, Health Collaborative Innovation Major Projects of Guangzhou City, Science and Technology Planning Project of Guangdong Province. Elsevier 2019-10-23 /pmc/articles/PMC6945279/ /pubmed/31668569 http://dx.doi.org/10.1016/j.ebiom.2019.09.039 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Chen, Shan
Zhao, Ke
Lin, Ren
Wang, Shunqing
Fan, Zhiping
Huang, Fen
Chen, Xiaoyong
Nie, Danian
Du, Xin
Guo, Ziwen
Lin, Dongjun
Xuan, Li
Xu, Na
Sun, Jing
Peng Xiang, Andy
Liu, Qifa
The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study
title The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study
title_full The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study
title_fullStr The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study
title_full_unstemmed The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study
title_short The efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic HSCT: A multicenter prospective cohort study
title_sort efficacy of mesenchymal stem cells in bronchiolitis obliterans syndrome after allogeneic hsct: a multicenter prospective cohort study
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945279/
https://www.ncbi.nlm.nih.gov/pubmed/31668569
http://dx.doi.org/10.1016/j.ebiom.2019.09.039
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