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CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性

OBJECTIVE: To investigate the efficacy and safety of CD19 chimeric antigen receptor T (CAR-T) lymphocytes for the treatment of B cell lymphoma. METHODS: A total of 22 patients with B-cell lymphoma from February 1, 2017 to July 1, 2018 were reviewed to evaluate the efficacy and adverse reactions of C...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343005/
https://www.ncbi.nlm.nih.gov/pubmed/31104437
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.04.003
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description OBJECTIVE: To investigate the efficacy and safety of CD19 chimeric antigen receptor T (CAR-T) lymphocytes for the treatment of B cell lymphoma. METHODS: A total of 22 patients with B-cell lymphoma from February 1, 2017 to July 1, 2018 were reviewed to evaluate the efficacy and adverse reactions of CD19 CAR-T. RESULTS: Of 22 patients with B-cell lymphoma received CD19 CAR-T cells, the median dose of CAR-T cells was 7.2 (2.0–12.0) ×10(6)/kg. Nine of 12 cases of relapse refractory patients were overall response. Complete remission (CR) occurred in 2 of 12 patients, partial remission (PR) in 7 of 12 patients. The overall response in minor residual disease positive (MRD) group was 8 of 10 patients. CD19 CAR-T cells proliferated in vivo and were detectable in the blood of patients. The peak timepoints of CAR-T cells proliferated in the relapsed refractory and MRD positive groups were 12 (5–19) and 4.5 (1–12) days after treatment respectively, and among peripheral blood cells, CAR-T cells accounted for 10.10% (3.55%–24.74%) and 4.02% (2.23%–28.60%) of T lymphocytes respectively. The MRD positive patients achieved sustained remissions during a median follow-up of 8 months (rang 3–18 months). None of all the patients relapsed during a median follow-up time of 10 months (3–18 months). However, 7 PR responders of the relapsed refractory patients maintained a good condition for 1.5–6.0 months. One patient bridged to hematopoietic stem cell transplantation, another one sustained remission for 12 months. Cytokine-release syndrome (CRS) occurred in 14 patients with grade 1–2 CRS in MRD positive group and grade 3 CRS in relapsed refractory group. CONCLUSION: CAR-T cell therapy not only played a role in the rescue treatment of relapsed and refractory patients, but also produced a surprising effect in the consolidation and maintenance of B-cell lymphoma. CD19 CAR-T cells might be more effective in the treatment of MRD positive B-cell lymphoma patients than in the refractory or relapsed cases. High response rate was observed with fewer adverse reactions.
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spelling pubmed-73430052020-07-16 CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To investigate the efficacy and safety of CD19 chimeric antigen receptor T (CAR-T) lymphocytes for the treatment of B cell lymphoma. METHODS: A total of 22 patients with B-cell lymphoma from February 1, 2017 to July 1, 2018 were reviewed to evaluate the efficacy and adverse reactions of CD19 CAR-T. RESULTS: Of 22 patients with B-cell lymphoma received CD19 CAR-T cells, the median dose of CAR-T cells was 7.2 (2.0–12.0) ×10(6)/kg. Nine of 12 cases of relapse refractory patients were overall response. Complete remission (CR) occurred in 2 of 12 patients, partial remission (PR) in 7 of 12 patients. The overall response in minor residual disease positive (MRD) group was 8 of 10 patients. CD19 CAR-T cells proliferated in vivo and were detectable in the blood of patients. The peak timepoints of CAR-T cells proliferated in the relapsed refractory and MRD positive groups were 12 (5–19) and 4.5 (1–12) days after treatment respectively, and among peripheral blood cells, CAR-T cells accounted for 10.10% (3.55%–24.74%) and 4.02% (2.23%–28.60%) of T lymphocytes respectively. The MRD positive patients achieved sustained remissions during a median follow-up of 8 months (rang 3–18 months). None of all the patients relapsed during a median follow-up time of 10 months (3–18 months). However, 7 PR responders of the relapsed refractory patients maintained a good condition for 1.5–6.0 months. One patient bridged to hematopoietic stem cell transplantation, another one sustained remission for 12 months. Cytokine-release syndrome (CRS) occurred in 14 patients with grade 1–2 CRS in MRD positive group and grade 3 CRS in relapsed refractory group. CONCLUSION: CAR-T cell therapy not only played a role in the rescue treatment of relapsed and refractory patients, but also produced a surprising effect in the consolidation and maintenance of B-cell lymphoma. CD19 CAR-T cells might be more effective in the treatment of MRD positive B-cell lymphoma patients than in the refractory or relapsed cases. High response rate was observed with fewer adverse reactions. Editorial office of Chinese Journal of Hematology 2019-04 /pmc/articles/PMC7343005/ /pubmed/31104437 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.04.003 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性
title CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性
title_full CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性
title_fullStr CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性
title_full_unstemmed CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性
title_short CD19 CAR-T细胞治疗B细胞淋巴瘤22例疗效及安全性
title_sort cd19 car-t细胞治疗b细胞淋巴瘤22例疗效及安全性
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343005/
https://www.ncbi.nlm.nih.gov/pubmed/31104437
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.04.003
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