• 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 细胞疗法在血液系统恶性肿瘤中的临床作用、毒性和未解决的问题。

CAR T-Cell Therapy in Hematologic Malignancies: Clinical Role, Toxicity, and Unanswered Questions.

机构信息

Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.

出版信息

Am Soc Clin Oncol Educ Book. 2021 Mar;41:1-20. doi: 10.1200/EDBK_320085.

DOI:10.1200/EDBK_320085
PMID:33989023
Abstract

At the time of writing, five anti-CD19 CAR T-cell products are approved by the U.S. Food and Drug Administration for seven different indications in lymphoid malignancies, including B-cell non-Hodgkin lymphoma, pediatric B-cell acute lymphoblastic leukemia, and multiple myeloma. CAR T cells for chronic lymphocytic leukemia, acute myeloid leukemia, and less common malignancies such as T-cell lymphomas and Hodgkin lymphoma are being tested in early-phase clinical trials worldwide. The purpose of this overview is to describe the current landscape of CAR T cells in hematologic malignancies, outline their outcomes and toxicities, and explain the outstanding questions that remain to be addressed.

摘要

在撰写本文时,已有五种抗 CD19 CAR T 细胞产品获得美国食品和药物管理局批准,用于治疗七种不同的淋巴恶性肿瘤适应症,包括 B 细胞非霍奇金淋巴瘤、儿童 B 细胞急性淋巴细胞白血病和多发性骨髓瘤。用于慢性淋巴细胞白血病、急性髓系白血病以及 T 细胞淋巴瘤和霍奇金淋巴瘤等罕见恶性肿瘤的 CAR T 细胞正在全球进行早期临床试验。本文的目的是描述 CAR T 细胞在血液恶性肿瘤中的现状,概述其疗效和毒性,并解释仍需解决的悬而未决的问题。

相似文献

1
CAR T-Cell Therapy in Hematologic Malignancies: Clinical Role, Toxicity, and Unanswered Questions.嵌合抗原受体 T 细胞疗法在血液系统恶性肿瘤中的临床作用、毒性和未解决的问题。
Am Soc Clin Oncol Educ Book. 2021 Mar;41:1-20. doi: 10.1200/EDBK_320085.
2
Selecting the Optimal CAR-T for the Treatment of B-Cell Malignancies.选择最佳 CAR-T 细胞疗法治疗 B 细胞恶性肿瘤。
Curr Hematol Malig Rep. 2021 Feb;16(1):32-39. doi: 10.1007/s11899-021-00615-7. Epub 2021 Feb 25.
3
Efficiency of CD19 chimeric antigen receptor-modified T cells for treatment of B cell malignancies in phase I clinical trials: a meta-analysis.I期临床试验中CD19嵌合抗原受体修饰的T细胞治疗B细胞恶性肿瘤的疗效:一项荟萃分析。
Oncotarget. 2015 Oct 20;6(32):33961-71. doi: 10.18632/oncotarget.5582.
4
The severe cytokine release syndrome in phase I trials of CD19-CAR-T cell therapy: a systematic review.CD19-CAR-T 细胞治疗 I 期临床试验中的严重细胞因子释放综合征:系统评价。
Ann Hematol. 2018 Aug;97(8):1327-1335. doi: 10.1007/s00277-018-3368-8. Epub 2018 May 15.
5
Bispecific anti-CD20, anti-CD19 CAR T cells for relapsed B cell malignancies: a phase 1 dose escalation and expansion trial.双特异性抗 CD20、抗 CD19 CAR T 细胞治疗复发 B 细胞恶性肿瘤:1 期剂量递增和扩展试验。
Nat Med. 2020 Oct;26(10):1569-1575. doi: 10.1038/s41591-020-1081-3. Epub 2020 Oct 5.
6
[Adoptive immunotherapy utilizing anti-CD19 chimeric antigen receptor T-cells for B-cell malignancies].利用抗CD19嵌合抗原受体T细胞治疗B细胞恶性肿瘤的过继性免疫疗法
Rinsho Ketsueki. 2016;57(11):2365-2372. doi: 10.11406/rinketsu.57.2365.
7
B-cell depletion and remissions of malignancy along with cytokine-associated toxicity in a clinical trial of anti-CD19 chimeric-antigen-receptor-transduced T cells.嵌合抗原受体修饰 T 细胞抗 CD19 治疗的临床试验中,B 细胞耗竭和恶性肿瘤缓解,以及细胞因子相关毒性。
Blood. 2012 Mar 22;119(12):2709-20. doi: 10.1182/blood-2011-10-384388. Epub 2011 Dec 8.
8
CAR-T Cell Therapies: An Overview of Clinical Studies Supporting Their Approved Use against Acute Lymphoblastic Leukemia and Large B-Cell Lymphomas.嵌合抗原受体 T 细胞疗法:支持其批准用于治疗急性淋巴细胞白血病和大 B 细胞淋巴瘤的临床研究概述。
Int J Mol Sci. 2020 May 30;21(11):3906. doi: 10.3390/ijms21113906.
9
Anti-CD19 CAR T-Cell Therapy for B-Cell Non-Hodgkin Lymphoma.抗 CD19 CAR T 细胞疗法治疗 B 细胞非霍奇金淋巴瘤。
Transfus Med Rev. 2020 Jan;34(1):29-33. doi: 10.1016/j.tmrv.2019.08.003. Epub 2019 Aug 29.
10
Axicabtagene ciloleucel for the treatment of relapsed/refractory B-cell non-Hodgkin's lymphomas.阿基仑赛注射液用于治疗复发/难治性B细胞非霍奇金淋巴瘤。
Drugs Today (Barc). 2018 Mar;54(3):187-198. doi: 10.1358/dot.2018.54.3.2776625.

引用本文的文献

1
Bridging intensity is associated with impaired hematopoietic recovery after BCMA CAR-T therapy for multiple myeloma.桥接强度与多发性骨髓瘤患者接受BCMA嵌合抗原受体T细胞(CAR-T)治疗后造血恢复受损有关。
Blood Adv. 2025 Aug 26;9(16):4151-4166. doi: 10.1182/bloodadvances.2024015732.
2
Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence.嵌合抗原受体T细胞疗法后血液系统恶性肿瘤患者的癌症相关认知障碍:患病率的系统评价和荟萃分析
Support Care Cancer. 2025 Mar 22;33(4):312. doi: 10.1007/s00520-025-09356-2.
3
Ultrasound and Photoacoustic Imaging of Nanoparticle-Engineered T Cells and Post-Treatment Assessment to Guide Adoptive Cell Immunotherapy.
纳米颗粒工程化T细胞的超声和光声成像以及用于指导过继性细胞免疫治疗的治疗后评估
ACS Nano. 2025 Feb 18;19(6):6079-6094. doi: 10.1021/acsnano.4c12929. Epub 2025 Feb 5.
4
Inhibition of furin in CAR macrophages directs them toward a proinflammatory phenotype and enhances their antitumor activities.抑制CAR巨噬细胞中的弗林蛋白酶可使其转向促炎表型并增强其抗肿瘤活性。
Cell Death Dis. 2024 Dec 4;15(12):879. doi: 10.1038/s41419-024-07267-4.
5
Targeting regulated cell death pathways in cancers for effective treatment: a comprehensive review.靶向癌症中受调控的细胞死亡途径以实现有效治疗:全面综述
Front Cell Dev Biol. 2024 Nov 15;12:1462339. doi: 10.3389/fcell.2024.1462339. eCollection 2024.
6
Improved safety of chimeric antigen receptor T cells indirectly targeting antigens via switchable adapters.通过可切换接头间接靶向抗原的嵌合抗原受体 T 细胞的安全性提高。
Nat Commun. 2024 Nov 18;15(1):9917. doi: 10.1038/s41467-024-53996-7.
7
Innovative virtual screening of PD-L1 inhibitors: the synergy of molecular similarity, neural networks and GNINA docking.PD-L1 抑制剂的创新虚拟筛选:分子相似性、神经网络和 GNINA 对接的协同作用。
Future Med Chem. 2024;16(20):2107-2118. doi: 10.1080/17568919.2024.2389773. Epub 2024 Sep 4.
8
Rational combinatorial targeting by adapter CAR-T-cells (AdCAR-T) prevents antigen escape in acute myeloid leukemia.通过适配器 CAR-T 细胞(AdCAR-T)进行合理的组合靶向可防止急性髓系白血病中的抗原逃逸。
Leukemia. 2024 Oct;38(10):2183-2195. doi: 10.1038/s41375-024-02351-2. Epub 2024 Aug 3.
9
Engineering of potent CAR NK cells using non-viral Sleeping Beauty transposition from minimalistic DNA vectors.使用最小化 DNA 载体的非病毒睡眠美人转座子工程化有效的 CAR NK 细胞。
Mol Ther. 2024 Jul 3;32(7):2357-2372. doi: 10.1016/j.ymthe.2024.05.022. Epub 2024 May 14.
10
TOP CAR with TMIGD2 as a safe and effective costimulatory domain in CAR cells treating human solid tumors.TOP 嵌合抗原受体(CAR)细胞以 TMIGD2 作为安全有效的共刺激结构域治疗人实体瘤。
Sci Adv. 2024 May 10;10(19):eadk1857. doi: 10.1126/sciadv.adk1857. Epub 2024 May 8.