• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

嵌合抗原受体T细胞(CAR-T细胞)治疗T细胞急性淋巴细胞白血病/淋巴瘤的临床疗效与安全性

Clinical outcomes and safety of CAR-T cells in treatment of T-Cell acute lymphoblastic leukemia/lymphoma.

作者信息

Ma Jin-Feng, Yan Chun-Long, Jia Xu, Zhu Hong-Jia, Yan Jia-Wei, Liu Mei-Jing, Zhang Dai-Yi, Liu Shen-Hao, Xu Nan, Zhang Hai-Guo, Ye Ling, Yu Lei, Wu De-Pei, Gong Wen-Jie, Dai Hai-Ping, Xue Sheng-Li

机构信息

Jining No.1 People'hospital, Jining, China.

National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Ann Hematol. 2025 Jan;104(1):57-63. doi: 10.1007/s00277-024-06132-w. Epub 2024 Dec 18.

DOI:10.1007/s00277-024-06132-w
PMID:39692783
Abstract

Relapsed or refractory T-cell acute lymphoblastic leukemia/lymphoma (r/r T-ALL/LBL) are frequently aggressive and associated with unfavorable prognoses. Pan-targeted Chimeric Antigen Receptor (CAR) T-cell therapy have shown promising results in clinical trials. In recent years, CD7 CAR T-cell and CD5 CAR T-cell demonstrate effectiveness in treating r/r T-ALL/LBL patients with bone marrow infiltration. However, nearly half of r/r T-ALL/T-LBL patients are accompanied by extramedullary disease (EMD), where comprehensive data on the efficacy and safety of CAR T-cell therapy remain limited. Additionally, CD7 CAR T-cell and CD5 CAR T-cell therapy can cause severe immunodeficiency and hematologic toxicity, complicating with difficult immune reconstitution. This review provides an in-depth analysis of the safety profile and adverse events associated with CAR T-cell therapy in r/r T-ALL/LBL, with a a particular emphasis on its impact in patients with EMD.

摘要

复发或难治性T细胞急性淋巴细胞白血病/淋巴瘤(r/r T-ALL/LBL)通常具有侵袭性,预后不良。全靶向嵌合抗原受体(CAR)T细胞疗法在临床试验中已显示出有前景的结果。近年来,CD7 CAR T细胞和CD5 CAR T细胞在治疗有骨髓浸润的r/r T-ALL/LBL患者中显示出有效性。然而,近一半的r/r T-ALL/T-LBL患者伴有髓外疾病(EMD),关于CAR T细胞疗法疗效和安全性的全面数据仍然有限。此外,CD7 CAR T细胞和CD5 CAR T细胞疗法可导致严重免疫缺陷和血液学毒性,伴有免疫重建困难。本综述深入分析了r/r T-ALL/LBL中与CAR T细胞疗法相关的安全性和不良事件,特别强调其对EMD患者的影响。

相似文献

1
Clinical outcomes and safety of CAR-T cells in treatment of T-Cell acute lymphoblastic leukemia/lymphoma.嵌合抗原受体T细胞(CAR-T细胞)治疗T细胞急性淋巴细胞白血病/淋巴瘤的临床疗效与安全性
Ann Hematol. 2025 Jan;104(1):57-63. doi: 10.1007/s00277-024-06132-w. Epub 2024 Dec 18.
2
Clinical Outcomes of CD7 CAR-T Cell Therapy in Relapsed or Refractory T-Cell Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma Patients.CD7嵌合抗原受体T细胞疗法在复发或难治性T细胞急性淋巴细胞白血病和淋巴细胞淋巴瘤患者中的临床疗效
Hematol Oncol. 2025 May;43(3):e70081. doi: 10.1002/hon.70081.
3
Donor-Derived CD7 Chimeric Antigen Receptor T Cells for T-Cell Acute Lymphoblastic Leukemia: First-in-Human, Phase I Trial.供体来源的 CD7 嵌合抗原受体 T 细胞治疗 T 细胞急性淋巴细胞白血病:首次人体、I 期临床试验。
J Clin Oncol. 2021 Oct 20;39(30):3340-3351. doi: 10.1200/JCO.21.00389. Epub 2021 Jul 29.
4
Case report: Preventive infusion of donor-derived CD7 chimeric antigen receptor T cells after allogeneic hematopoietic stem cell transplantation.病例报告:异基因造血干细胞移植后供体来源的 CD7 嵌合抗原受体 T 细胞的预防性输注。
Front Immunol. 2024 Apr 30;15:1381308. doi: 10.3389/fimmu.2024.1381308. eCollection 2024.
5
A safety and efficacy study of allogeneic haematopoietic stem cell transplantation for refractory and relapsed T-cell acute lymphoblastic leukaemia/lymphoblastic lymphoma patients who achieved complete remission after autologous CD7 chimeric antigen receptor T-cell therapy.异基因造血干细胞移植治疗自体 CD7 嵌合抗原受体 T 细胞治疗后达到完全缓解的难治性和复发性 T 细胞急性淋巴细胞白血病/淋巴母细胞淋巴瘤患者的安全性和疗效研究。
Br J Haematol. 2024 Jun;204(6):2351-2364. doi: 10.1111/bjh.19445. Epub 2024 Apr 13.
6
Case report: CD7-targeted autologous CAR-T therapy for the treatment of T-cell acute lymphoblastic leukemia undergoing allogeneic peripheral blood stem cell transplantation in the long-term follow-up.病例报告:靶向CD7的自体嵌合抗原受体T细胞疗法用于治疗接受异基因外周血干细胞移植的T细胞急性淋巴细胞白血病的长期随访
Front Immunol. 2024 Nov 15;15:1469251. doi: 10.3389/fimmu.2024.1469251. eCollection 2024.
7
Analysis of 60 patients with relapsed or refractory T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma treated with CD7-targeted chimeric antigen receptor-T cell therapy.CD7 靶向嵌合抗原受体 T 细胞疗法治疗复发或难治性 T 细胞急性淋巴细胞白血病和 T 细胞淋巴母细胞淋巴瘤患者 60 例分析。
Am J Hematol. 2023 Dec;98(12):1898-1908. doi: 10.1002/ajh.27094. Epub 2023 Sep 23.
8
Single-Cell Transcriptomics Reveals Immune Reconstitution in Patients with R/R T-ALL/LBL Treated with Donor-Derived CD7 CAR-T Therapy.单细胞转录组学揭示了接受供体来源 CD7 CAR-T 治疗的复发/难治性 T-ALL/LBL 患者的免疫重建。
Clin Cancer Res. 2023 Apr 14;29(8):1484-1495. doi: 10.1158/1078-0432.CCR-22-2924.
9
SOHO State of the Art Updates and Next Questions | CAR T Cells in T Cell Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma.SOHO最新技术进展与后续问题 | T细胞急性淋巴细胞白血病和淋巴细胞淋巴瘤中的嵌合抗原受体T细胞
Clin Lymphoma Myeloma Leuk. 2025 Feb;25(2):77-88. doi: 10.1016/j.clml.2024.05.018. Epub 2024 May 31.
10
Chimeric antigen receptor T-cell therapy for T-cell acute lymphoblastic leukemia.嵌合抗原受体 T 细胞疗法治疗 T 细胞急性淋巴细胞白血病。
Haematologica. 2024 Jun 1;109(6):1677-1688. doi: 10.3324/haematol.2023.283848.

引用本文的文献

1
Research progress on chimeric antigen receptor-based immunotherapy against autoimmune diseases.基于嵌合抗原受体的自身免疫性疾病免疫治疗研究进展
Hum Vaccin Immunother. 2025 Dec;21(1):2538350. doi: 10.1080/21645515.2025.2538350. Epub 2025 Aug 1.
2
Venetoclax and azacitidine in combination with homoharringtonine, cytarabine, and aclarubicin for salvage therapy of relapsed/refractory T cell acute lymphoblastic leukemia.维奈托克与阿扎胞苷联合高三尖杉酯碱、阿糖胞苷和阿柔比星用于复发/难治性T细胞急性淋巴细胞白血病的挽救治疗。
Int J Hematol. 2025 Apr;121(4):547-552. doi: 10.1007/s12185-025-03915-3. Epub 2025 Jan 23.

本文引用的文献

1
Safe and potent anti-CD19 CAR T-cells with shRNA-IL-6 gene silencing element in patients with refractory or relapsed B-cell acute lymphoblastic leukemia.在难治性或复发性B细胞急性淋巴细胞白血病患者中具有shRNA-IL-6基因沉默元件的安全有效的抗CD19嵌合抗原受体T细胞。
Hemasphere. 2024 Oct 7;8(10):e70007. doi: 10.1002/hem3.70007. eCollection 2024 Oct.
2
Sequential CD7 CAR T-Cell Therapy and Allogeneic HSCT without GVHD Prophylaxis.序贯 CD7 CAR T 细胞治疗与异基因造血干细胞移植而不进行移植物抗宿主病预防。
N Engl J Med. 2024 Apr 25;390(16):1467-1480. doi: 10.1056/NEJMoa2313812.
3
Analysis of 60 patients with relapsed or refractory T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma treated with CD7-targeted chimeric antigen receptor-T cell therapy.
CD7 靶向嵌合抗原受体 T 细胞疗法治疗复发或难治性 T 细胞急性淋巴细胞白血病和 T 细胞淋巴母细胞淋巴瘤患者 60 例分析。
Am J Hematol. 2023 Dec;98(12):1898-1908. doi: 10.1002/ajh.27094. Epub 2023 Sep 23.
4
Allogenic and autologous anti-CD7 CAR-T cell therapies in relapsed or refractory T-cell malignancies.异体和自体抗 CD7 CAR-T 细胞疗法治疗复发或难治性 T 细胞恶性肿瘤。
Blood Cancer J. 2023 Apr 25;13(1):61. doi: 10.1038/s41408-023-00822-w.
5
Long-term follow-up of donor-derived CD7 CAR T-cell therapy in patients with T-cell acute lymphoblastic leukemia.供体来源 CD7 CAR T 细胞治疗 T 细胞急性淋巴细胞白血病患者的长期随访。
J Hematol Oncol. 2023 Apr 5;16(1):34. doi: 10.1186/s13045-023-01427-3.
6
Selective homing of CAR-CIK cells to the bone marrow niche enhances control of the acute myeloid leukemia burden.CAR-CIK 细胞对骨髓龛的选择性归巢增强了对急性髓系白血病负担的控制。
Blood. 2023 May 25;141(21):2587-2598. doi: 10.1182/blood.2022018330.
7
Single-Cell Transcriptomics Reveals Immune Reconstitution in Patients with R/R T-ALL/LBL Treated with Donor-Derived CD7 CAR-T Therapy.单细胞转录组学揭示了接受供体来源 CD7 CAR-T 治疗的复发/难治性 T-ALL/LBL 患者的免疫重建。
Clin Cancer Res. 2023 Apr 14;29(8):1484-1495. doi: 10.1158/1078-0432.CCR-22-2924.
8
The emerging scenario of immunotherapy for T-cell Acute Lymphoblastic Leukemia: advances, challenges and future perspectives.T细胞急性淋巴细胞白血病免疫治疗的新态势:进展、挑战与未来展望
Exp Hematol Oncol. 2023 Jan 9;12(1):5. doi: 10.1186/s40164-022-00368-w.
9
Donor CD7 Chimeric Antigen Receptor T Cell Bridging to Allogeneic Hematopoietic Stem Cell Transplantation for T Cell Hematologic Malignancy.供者 CD7 嵌合抗原受体 T 细胞桥接异基因造血干细胞移植治疗 T 细胞血液恶性肿瘤。
Transplant Cell Ther. 2023 Mar;29(3):167-173. doi: 10.1016/j.jtct.2022.11.013. Epub 2022 Nov 24.
10
Genetically modified CD7-targeting allogeneic CAR-T cell therapy with enhanced efficacy for relapsed/refractory CD7-positive hematological malignancies: a phase I clinical study.基因修饰的靶向 CD7 的同种异体嵌合抗原受体 T 细胞疗法增强了治疗复发/难治性 CD7 阳性血液系统恶性肿瘤的疗效:一项 I 期临床研究。
Cell Res. 2022 Nov;32(11):995-1007. doi: 10.1038/s41422-022-00721-y. Epub 2022 Sep 23.