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异基因造血干细胞移植后复发患者接受供体 CD19 CAR-T 细胞治疗的长期生存。

Long-term survival with donor CD19 CAR-T cell treatment for relapsed patients after allogeneic hematopietic stem cell transplantation.

机构信息

Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.

Chongqing Key Laboratory of Hematology and Microenvironment, Chongqing, 400037, China.

出版信息

J Hematol Oncol. 2024 Oct 29;17(1):103. doi: 10.1186/s13045-024-01626-6.

DOI:10.1186/s13045-024-01626-6
PMID:39468581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11520587/
Abstract

Chimeric Antigen Receptor T (CAR-T) cell therapy has significantly advanced in treating B-cell acute lymphoblastic leukemia (B-ALL) and has shown efficacy in managing relapsed B-ALL after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Donor-derived CAR-T cell offer both high efficacy and rapid response. Although promising results exist, current research lacks definitive evidence of long-term survival benefits for patients treated with donor-derived CAR-T therapy. We report the long-term survival of 32 patients with post-transplant relapsed B-ALL treated with donor-derived CD19 CAR-T cell, achieving either complete Remission (CR) or CR with incomplete peripheral blood recovery (CRi). The median follow-up was 42 months, with 2-year overall survival (OS) and event-free survival (EFS) rates of 56.25% and 50.0%, respectively. The 5-year OS and EFS rates were 53.13% and 46.88%, with no new long-term adverse events observed. These findings demonstrate good long-term safety, supporting donor-derived CAR-T cell as a recommended treatment option for relapsed B-ALL patients post-transplantation. Trial registration: https://www.chictr.org.cn/showproj.html?proj=14315 . Registration number: ChiCTR-OOC-16008447.

摘要

嵌合抗原受体 T(CAR-T)细胞疗法在治疗 B 细胞急性淋巴细胞白血病(B-ALL)方面取得了显著进展,并在异基因造血干细胞移植(allo-HSCT)后管理复发的 B-ALL 方面显示出疗效。供体来源的 CAR-T 细胞具有高效和快速反应的特点。尽管有令人鼓舞的结果,但目前的研究缺乏接受供体来源的 CAR-T 治疗的患者长期生存获益的确切证据。我们报告了 32 例接受供体来源的 CD19 CAR-T 细胞治疗的移植后复发 B-ALL 患者的长期生存情况,这些患者达到完全缓解(CR)或不完全外周血恢复的完全缓解(CRi)。中位随访时间为 42 个月,2 年总生存率(OS)和无事件生存率(EFS)分别为 56.25%和 50.0%。5 年 OS 和 EFS 率分别为 53.13%和 46.88%,未观察到新的长期不良事件。这些发现表明良好的长期安全性,支持供体来源的 CAR-T 细胞作为移植后复发 B-ALL 患者的推荐治疗选择。试验注册:https://www.chictr.org.cn/showproj.html?proj=14315。注册号:ChiCTR-OOC-16008447。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b56a/11520587/814a81d47bbb/13045_2024_1626_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b56a/11520587/814a81d47bbb/13045_2024_1626_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b56a/11520587/814a81d47bbb/13045_2024_1626_Fig1_HTML.jpg

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本文引用的文献

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EClinicalMedicine. 2023 Dec 21;67:102377. doi: 10.1016/j.eclinm.2023.102377. eCollection 2024 Jan.
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Donor-derived CD19 CAR-T Cells versus Chemotherapy Plus Donor Lymphocyte Infusion for Treatment of Recurrent CD19-positive B-ALL After Allogeneic Hematopoietic Stem Cell Transplantation.供者来源的 CD19 CAR-T 细胞与化疗加供者淋巴细胞输注治疗异基因造血干细胞移植后复发性 CD19 阳性 B-ALL。
Curr Med Sci. 2023 Aug;43(4):733-740. doi: 10.1007/s11596-023-2746-1. Epub 2023 Jun 17.
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Base-Edited CAR7 T Cells for Relapsed T-Cell Acute Lymphoblastic Leukemia.经碱基编辑的 CAR7 T 细胞治疗复发型 T 细胞急性淋巴细胞白血病。
N Engl J Med. 2023 Sep 7;389(10):899-910. doi: 10.1056/NEJMoa2300709. Epub 2023 Jun 14.
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