Cargando…
Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies
BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the cornerstone in treatment of hematological malignancies. However, relapse of the hematological disease after allo-HSCT remains a challenge and is associated with poor long-term survival. Chimeric antigen rece...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282795/ https://www.ncbi.nlm.nih.gov/pubmed/28143567 http://dx.doi.org/10.1186/s13045-017-0405-3 |
_version_ | 1782503394562277376 |
---|---|
author | Liu, Jun Zhong, Jiang F. Zhang, Xi Zhang, Cheng |
author_facet | Liu, Jun Zhong, Jiang F. Zhang, Xi Zhang, Cheng |
author_sort | Liu, Jun |
collection | PubMed |
description | BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the cornerstone in treatment of hematological malignancies. However, relapse of the hematological disease after allo-HSCT remains a challenge and is associated with poor long-term survival. Chimeric antigen receptor redirected T cells (CAR-T cells) can lead to disease remission in patients with relapsed/refractory hematological malignancies. However, the therapeutic window for infusion of CAR-T cells post allo-HSCT and its efficacy are debatable. MAIN BODY: In this review, we first discuss the use of CAR-T cells for relapsed cases after allo-HSCT. We then review the toxicities and the occurrence of graft-versus-host disease in relapsed patients who received CAR-T cells post allo-HSCT. Finally, we review clinical trial registrations and the therapeutic time window for infusion of CAR-T cells post allo-HSCT. CONCLUSIONS: The treatment of allogeneic CAR-T cells is beneficial for patients with relapsed B cell malignancies after allo-HSCT with low toxicities and complications. However, multicenter clinical trials with larger sample sizes should be performed to select the optimal therapeutic window and confirm its efficacy. |
format | Online Article Text |
id | pubmed-5282795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52827952017-02-03 Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies Liu, Jun Zhong, Jiang F. Zhang, Xi Zhang, Cheng J Hematol Oncol Review BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered the cornerstone in treatment of hematological malignancies. However, relapse of the hematological disease after allo-HSCT remains a challenge and is associated with poor long-term survival. Chimeric antigen receptor redirected T cells (CAR-T cells) can lead to disease remission in patients with relapsed/refractory hematological malignancies. However, the therapeutic window for infusion of CAR-T cells post allo-HSCT and its efficacy are debatable. MAIN BODY: In this review, we first discuss the use of CAR-T cells for relapsed cases after allo-HSCT. We then review the toxicities and the occurrence of graft-versus-host disease in relapsed patients who received CAR-T cells post allo-HSCT. Finally, we review clinical trial registrations and the therapeutic time window for infusion of CAR-T cells post allo-HSCT. CONCLUSIONS: The treatment of allogeneic CAR-T cells is beneficial for patients with relapsed B cell malignancies after allo-HSCT with low toxicities and complications. However, multicenter clinical trials with larger sample sizes should be performed to select the optimal therapeutic window and confirm its efficacy. BioMed Central 2017-01-31 /pmc/articles/PMC5282795/ /pubmed/28143567 http://dx.doi.org/10.1186/s13045-017-0405-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Liu, Jun Zhong, Jiang F. Zhang, Xi Zhang, Cheng Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies |
title | Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies |
title_full | Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies |
title_fullStr | Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies |
title_full_unstemmed | Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies |
title_short | Allogeneic CD19-CAR-T cell infusion after allogeneic hematopoietic stem cell transplantation in B cell malignancies |
title_sort | allogeneic cd19-car-t cell infusion after allogeneic hematopoietic stem cell transplantation in b cell malignancies |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282795/ https://www.ncbi.nlm.nih.gov/pubmed/28143567 http://dx.doi.org/10.1186/s13045-017-0405-3 |
work_keys_str_mv | AT liujun allogeneiccd19cartcellinfusionafterallogeneichematopoieticstemcelltransplantationinbcellmalignancies AT zhongjiangf allogeneiccd19cartcellinfusionafterallogeneichematopoieticstemcelltransplantationinbcellmalignancies AT zhangxi allogeneiccd19cartcellinfusionafterallogeneichematopoieticstemcelltransplantationinbcellmalignancies AT zhangcheng allogeneiccd19cartcellinfusionafterallogeneichematopoieticstemcelltransplantationinbcellmalignancies |