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Neurologic toxicities following adoptive immunotherapy with BCMA-directed CAR T cells.采用靶向BCMA的嵌合抗原受体T细胞进行过继性免疫治疗后的神经毒性。
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N Engl J Med. 2023 Jul 27;389(4):335-347. doi: 10.1056/NEJMoa2303379. Epub 2023 Jun 5.
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Transcriptome-based network analysis related to M2-like tumor-associated macrophage infiltration identified VARS1 as a potential target for improving melanoma immunotherapy efficacy.基于转录组的 M2 样肿瘤相关巨噬细胞浸润相关的网络分析鉴定 VARS1 为提高黑色素瘤免疫治疗疗效的潜在靶点。
J Transl Med. 2022 Oct 27;20(1):489. doi: 10.1186/s12967-022-03686-z.
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Ciltacabtagene Autoleucel, an Anti-B-cell Maturation Antigen Chimeric Antigen Receptor T-Cell Therapy, for Relapsed/Refractory Multiple Myeloma: CARTITUDE-1 2-Year Follow-Up.西达基奥仑赛,一种抗 B 细胞成熟抗原嵌合抗原受体 T 细胞疗法,用于治疗复发/难治性多发性骨髓瘤:CARTITUDE-1 研究 2 年随访结果。
J Clin Oncol. 2023 Feb 20;41(6):1265-1274. doi: 10.1200/JCO.22.00842. Epub 2022 Jun 4.
5
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Blood Cancer J. 2022 Feb 24;12(2):32. doi: 10.1038/s41408-022-00629-1.
6
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KTE-X19 for relapsed or refractory adult B-cell acute lymphoblastic leukaemia: phase 2 results of the single-arm, open-label, multicentre ZUMA-3 study.泽沃基奥仑赛注射液(KTE-X19)治疗复发或难治性成人 B 细胞急性淋巴细胞白血病:ZUMA-3 研究单臂、开放标签、多中心的 2 期结果。
Lancet. 2021 Aug 7;398(10299):491-502. doi: 10.1016/S0140-6736(21)01222-8. Epub 2021 Jun 4.
9
Idecabtagene Vicleucel in Relapsed and Refractory Multiple Myeloma.伊达比星脂质体注射用多柔比星治疗复发/难治性多发性骨髓瘤
N Engl J Med. 2021 Feb 25;384(8):705-716. doi: 10.1056/NEJMoa2024850.
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ASTCT Consensus Grading for Cytokine Release Syndrome and Neurologic Toxicity Associated with Immune Effector Cells.ASTCT 细胞因子释放综合征和免疫效应细胞相关神经系统毒性的共识分级标准。
Biol Blood Marrow Transplant. 2019 Apr;25(4):625-638. doi: 10.1016/j.bbmt.2018.12.758. Epub 2018 Dec 25.

化疗诱导的 cilta-cabtagene autoleucel 相关运动和神经认知毒性逆转。

Chemotherapy-induced reversal of ciltacabtagene autoleucel-associated movement and neurocognitive toxicity.

机构信息

Cellular Immunotherapy Program, Cancer Center, Massachusetts General Hospital, Boston, MA.

Department of Medicine, Harvard Medical School, Boston, MA.

出版信息

Blood. 2023 Oct 5;142(14):1248-1252. doi: 10.1182/blood.2023021429.

DOI:10.1182/blood.2023021429
PMID:37467494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10579042/
Abstract

In 2 complementary Letters to Blood, Karschnia et al and Graham et al provide new insights into the neurological toxicities that are observed with B-cell maturation antigen–directed chimeric antigen receptor T-cell treatment for multiple myeloma, identifying a frequency of immune effector cell–associated neurotoxicity syndrome (ICANS) that exceeds 40%. Severe ICANS is identified in 8% of patients in this real-world series. Outcomes were generally favorable, although the authors describe rare, late Parkinsonism-like hypokinetic movement disorders (also known as movement and neurocognitive toxicities) post-ICANS in 2 patients.

摘要

在《Blood》杂志的 2 封补充信件中,Karschnia 等人和 Graham 等人提供了多发性骨髓瘤中 B 细胞成熟抗原导向嵌合抗原受体 T 细胞治疗所观察到的神经毒性的新见解,确定了细胞相关性神经毒性综合征(ICANS)的频率超过 40%。在这个真实世界的系列中,有 8%的患者出现严重的 ICANS。尽管作者描述了 2 例患者在发生 ICANS 后出现罕见的迟发性帕金森样运动障碍(也称为运动和神经认知毒性),但结果通常是有利的。