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Título
Treatment of post-allogeneic hematopoietic stem cell transplant cytopenias with sequential doses of multipotent mesenchymal stromal/stem cells
Autor(es)
Palabras clave
allogeneic hematopoietic transplantation; bone marrow multipotent mesenchymal stromal/stem cells; mesenchymal stromal cells; mesenchymal stem cells; MSC; cytopenias
allogeneic hematopoietic transplantation
bone marrow multipotent mesenchymal stromal/stem cells
mesenchymal stromal cells
mesenchymal stem cells
cytopenias
Clasificación UNESCO
3205.04 Hematología
Fecha de publicación
2024-08
Editor
Elsevier Inc
Citación
Navarro-Bailón A, López-Parra M, Veiga-Vaz Á, Villarón EM, Díez-Campelo M, Martín AÁ, Pérez-López E, Cabrero M, Vázquez L, López-Corral L, Sánchez-Guijo F. Treatment of post-allogeneic hematopoietic stem cell transplant cytopenias with sequential doses of multipotent mesenchymal stromal/stem cells. Cytotherapy. 2024 Aug;26(8):806-812. doi: 10.1016/j.jcyt.2024.04.006. Epub 2024 Apr 21. PMID: 38727653.
Resumen
[EN]Background aims: Cytopenias after allogeneic stem cell transplantation (allo-SCT) are a common complication, the underlying pathogenic mechanisms of which remain incompletely understood. Multipotent mesenchymal stromal/stem cell (MSC) therapy has been successfully employed in the treatment of immune related disorders and can aid in the restoration of the hematopoietic niche.
Methods: A phase II clinical trial to assess the efficacy and safety of administering four sequential doses of ex-vivo expanded bone marrow MSCs from a third-party donor to patients with persistent severe cytopenias after allo-SCT was performed.
Results: The overall response rate on day 90 was 75% among the 27 evaluable patients (comprising 12 complete responses, 8 partial responses, and 7 with no response). The median time to respond was 14.5 days. Responses were observed across different profiles, including single or multiple affected lineages, primary or secondary timing, and potential immune-mediated or post-infectious pathophysiology versus idiopathic origin. With a median follow-up for surviving patients of 85 months after MSC infusion, 53% of patients are alive. Notably, no adverse events related to MSC therapy were reported.
Conclusions: In summary, the sequential infusion of third-party MSCs emerges as a viable and safe therapeutic option, exhibiting potential benefits for patients experiencing cytopenias following allo-SCT.
URI
ISSN
1465-3249
DOI
10.1016/j.jcyt.2024.04.006
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