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Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients
This study aimed to evaluate treatment response, survival, safety profiles, and predictive factors to chimeric antigen receptor T cell (CAR-T) therapy in Chinese patients with relapsed or refractory B cell acute lymphoblast leukemia (R/R B-ALL). 39R/R B-ALL patients who underwent CAR-T therapy were...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105502/ https://www.ncbi.nlm.nih.gov/pubmed/32231200 http://dx.doi.org/10.1038/s41419-020-2388-1 |
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author | Li, Limin Liu, Jie Xu, Mengyuan Yu, Hongjuan Lv, Chengfang Cao, Fenglin Wang, Zhenkun Fu, Yueyue Zhang, Mingwen Meng, Hongbin Zhang, Xiaoqian Kang, Liqing Zhang, Zhuo Li, Jinmei Feng, Jiawei Lian, Xin Yu, Lei Zhou, Jin |
author_facet | Li, Limin Liu, Jie Xu, Mengyuan Yu, Hongjuan Lv, Chengfang Cao, Fenglin Wang, Zhenkun Fu, Yueyue Zhang, Mingwen Meng, Hongbin Zhang, Xiaoqian Kang, Liqing Zhang, Zhuo Li, Jinmei Feng, Jiawei Lian, Xin Yu, Lei Zhou, Jin |
author_sort | Li, Limin |
collection | PubMed |
description | This study aimed to evaluate treatment response, survival, safety profiles, and predictive factors to chimeric antigen receptor T cell (CAR-T) therapy in Chinese patients with relapsed or refractory B cell acute lymphoblast leukemia (R/R B-ALL). 39R/R B-ALL patients who underwent CAR-T therapy were included. Baseline data were collected from patients’ electronic medical records. Patients’ peripheral bloods, bone marrow aspirates, and biopsies were obtained for routine examination, and treatment response and survival profiles as well as adverse events were evaluated. The rates of complete remission (CR), CR with minimal residual disease (MRD) negative/positive, and bridging to hematopoietic stem-cell transplantation (HSCT) were 92.3%, 76.9%, 15.4%, and 43.6%, respectively. The median event-free survival (EFS) was 11.6 months (95% confidence interval (CI): 4.0–19.2 months) and median overall survival (OS) was 14.0 months (95% CI: 10.9–17.1 months). Bridging to HSCT independently predicted better EFS and OS, while high bone marrow blasts level independently predicted worse EFS. The incidence of cytokine release syndrome (CRS) was 97.4%, and refractory disease as well as decreased white blood cell independently predicted higher risk of severe CRS. Other common adverse events included hematologic toxicities (grade I: 5.1%, grade II: 7.7%, grade III: 17.9%, grade IV: 69.2%), neurotoxicity (28.2%), infection (38.5%), and admission for intensive care unit (10.3%). In conclusion, CAR-T therapy presents with promising treatment response, survival and safety profiles, and higher disease burden predicts worse survival as well as increased risk of severe CRS in Chinese R/R B-ALL patients. |
format | Online Article Text |
id | pubmed-7105502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71055022020-03-31 Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients Li, Limin Liu, Jie Xu, Mengyuan Yu, Hongjuan Lv, Chengfang Cao, Fenglin Wang, Zhenkun Fu, Yueyue Zhang, Mingwen Meng, Hongbin Zhang, Xiaoqian Kang, Liqing Zhang, Zhuo Li, Jinmei Feng, Jiawei Lian, Xin Yu, Lei Zhou, Jin Cell Death Dis Article This study aimed to evaluate treatment response, survival, safety profiles, and predictive factors to chimeric antigen receptor T cell (CAR-T) therapy in Chinese patients with relapsed or refractory B cell acute lymphoblast leukemia (R/R B-ALL). 39R/R B-ALL patients who underwent CAR-T therapy were included. Baseline data were collected from patients’ electronic medical records. Patients’ peripheral bloods, bone marrow aspirates, and biopsies were obtained for routine examination, and treatment response and survival profiles as well as adverse events were evaluated. The rates of complete remission (CR), CR with minimal residual disease (MRD) negative/positive, and bridging to hematopoietic stem-cell transplantation (HSCT) were 92.3%, 76.9%, 15.4%, and 43.6%, respectively. The median event-free survival (EFS) was 11.6 months (95% confidence interval (CI): 4.0–19.2 months) and median overall survival (OS) was 14.0 months (95% CI: 10.9–17.1 months). Bridging to HSCT independently predicted better EFS and OS, while high bone marrow blasts level independently predicted worse EFS. The incidence of cytokine release syndrome (CRS) was 97.4%, and refractory disease as well as decreased white blood cell independently predicted higher risk of severe CRS. Other common adverse events included hematologic toxicities (grade I: 5.1%, grade II: 7.7%, grade III: 17.9%, grade IV: 69.2%), neurotoxicity (28.2%), infection (38.5%), and admission for intensive care unit (10.3%). In conclusion, CAR-T therapy presents with promising treatment response, survival and safety profiles, and higher disease burden predicts worse survival as well as increased risk of severe CRS in Chinese R/R B-ALL patients. Nature Publishing Group UK 2020-03-30 /pmc/articles/PMC7105502/ /pubmed/32231200 http://dx.doi.org/10.1038/s41419-020-2388-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Limin Liu, Jie Xu, Mengyuan Yu, Hongjuan Lv, Chengfang Cao, Fenglin Wang, Zhenkun Fu, Yueyue Zhang, Mingwen Meng, Hongbin Zhang, Xiaoqian Kang, Liqing Zhang, Zhuo Li, Jinmei Feng, Jiawei Lian, Xin Yu, Lei Zhou, Jin Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients |
title | Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients |
title_full | Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients |
title_fullStr | Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients |
title_full_unstemmed | Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients |
title_short | Treatment response, survival, safety, and predictive factors to chimeric antigen receptor T cell therapy in Chinese relapsed or refractory B cell acute lymphoblast leukemia patients |
title_sort | treatment response, survival, safety, and predictive factors to chimeric antigen receptor t cell therapy in chinese relapsed or refractory b cell acute lymphoblast leukemia patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105502/ https://www.ncbi.nlm.nih.gov/pubmed/32231200 http://dx.doi.org/10.1038/s41419-020-2388-1 |
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