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Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis

Purpose: Chimeric Antigen Receptor T(CAR-T) cell therapy is an immunotherapy approach used in treating cancer which has seen rapid development over the decades. It becomes the preferred treatment choice after patients have failed conventional chemotherapy. Methods: We conducted a meta-analysis in 32...

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Autores principales: Drokow, Emmanuel Kwateng, Ahmed, Hafiz Abdul Waqas, Amponsem-Boateng, Cecilia, Akpabla, Gloria Selorm, Song, Juanjuan, Shi, Mingyue, Sun, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511615/
https://www.ncbi.nlm.nih.gov/pubmed/31190844
http://dx.doi.org/10.2147/TCRM.S203822
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author Drokow, Emmanuel Kwateng
Ahmed, Hafiz Abdul Waqas
Amponsem-Boateng, Cecilia
Akpabla, Gloria Selorm
Song, Juanjuan
Shi, Mingyue
Sun, Kai
author_facet Drokow, Emmanuel Kwateng
Ahmed, Hafiz Abdul Waqas
Amponsem-Boateng, Cecilia
Akpabla, Gloria Selorm
Song, Juanjuan
Shi, Mingyue
Sun, Kai
author_sort Drokow, Emmanuel Kwateng
collection PubMed
description Purpose: Chimeric Antigen Receptor T(CAR-T) cell therapy is an immunotherapy approach used in treating cancer which has seen rapid development over the decades. It becomes the preferred treatment choice after patients have failed conventional chemotherapy. Methods: We conducted a meta-analysis in 320 patients from 14 studies to estimate the survival outcome, response rate and toxicity of autologous CD19 CAR-T cell therapy and predict other factors associated with a better prognosis. Results: The overall response rate was 71.88% (95% CI: 61.34–80.46%, p<0.01) and CRS toxicity was 60.15% (95% CI: 42.87–75.22%, p<0.01). Patients who received lymphodepletion was associated with a better response rate (77%, 95%CI: 67–83%; p-value =0.001) in comparison to the other patients who did not (66%, 95%CI: 41–83%). Conclusion: Lymphodepletion regimen may play a crucial role in predicting the prognosis of patients with hematological malignancies. Lymphodepletion patients had better progression-free survival than those who did not.
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spelling pubmed-65116152019-06-12 Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis Drokow, Emmanuel Kwateng Ahmed, Hafiz Abdul Waqas Amponsem-Boateng, Cecilia Akpabla, Gloria Selorm Song, Juanjuan Shi, Mingyue Sun, Kai Ther Clin Risk Manag Original Research Purpose: Chimeric Antigen Receptor T(CAR-T) cell therapy is an immunotherapy approach used in treating cancer which has seen rapid development over the decades. It becomes the preferred treatment choice after patients have failed conventional chemotherapy. Methods: We conducted a meta-analysis in 320 patients from 14 studies to estimate the survival outcome, response rate and toxicity of autologous CD19 CAR-T cell therapy and predict other factors associated with a better prognosis. Results: The overall response rate was 71.88% (95% CI: 61.34–80.46%, p<0.01) and CRS toxicity was 60.15% (95% CI: 42.87–75.22%, p<0.01). Patients who received lymphodepletion was associated with a better response rate (77%, 95%CI: 67–83%; p-value =0.001) in comparison to the other patients who did not (66%, 95%CI: 41–83%). Conclusion: Lymphodepletion regimen may play a crucial role in predicting the prognosis of patients with hematological malignancies. Lymphodepletion patients had better progression-free survival than those who did not. Dove 2019-05-06 /pmc/articles/PMC6511615/ /pubmed/31190844 http://dx.doi.org/10.2147/TCRM.S203822 Text en © 2019 Drokow et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Drokow, Emmanuel Kwateng
Ahmed, Hafiz Abdul Waqas
Amponsem-Boateng, Cecilia
Akpabla, Gloria Selorm
Song, Juanjuan
Shi, Mingyue
Sun, Kai
Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
title Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
title_full Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
title_fullStr Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
title_full_unstemmed Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
title_short Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
title_sort survival outcomes and efficacy of autologous cd19 chimeric antigen receptor-t cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511615/
https://www.ncbi.nlm.nih.gov/pubmed/31190844
http://dx.doi.org/10.2147/TCRM.S203822
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