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嵌合抗原受体T细胞疗法与急性淋巴细胞白血病治疗中神经并发症之间的斗争

The Struggle Between Chimeric Antigen Receptor T-Cell Therapy and Neurological Complications in Acute Lymphoblastic Leukemia Treatment.

作者信息

Kubick Norwin, Łazarczyk Marzena, Awad Omar, Ławiński Michał, Horbańczuk Jarosław Olav, Sacharczuk Mariusz, Atanasov Atanas G, Religa Piotr, Mickael Michel Edwar

机构信息

Department of Biology, Institute of Plant Science and Microbiology, University of Hamburg, Ohnhorststr. 18, 22609 Hamburg, Germany.

Institute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Postepu 36A, 05-552 Jastrzebiec, Poland.

出版信息

Curr Issues Mol Biol. 2025 May 21;47(5):381. doi: 10.3390/cimb47050381.

Abstract

Acute lymphoblastic leukemia (ALL) accounts for approximately 25% of childhood cancers and 20% of leukemia cases in adults, with a higher prevalence in males than females. It is characterized by symptoms such as fatigue, fever, and bone pain and poses a significant risk of mortality if left untreated. While chemotherapy and stem cell transplantation are standard treatments, their efficacy declines in relapsed or refractory cases, highlighting the need for innovative therapeutic approaches. CAR T-cell therapy has emerged as a transformative technology, offering the potential to overcome these challenges and deliver durable remissions. CAR T-cell therapy demonstrates significant advantages, including targeting specific antigens, overcoming high-risk genetic mutations, and achieving sustained remissions in both pediatric and adult patients. However, notable challenges remain, such as cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). In this review, we focus on neurological symptoms associated with CAR T-cell therapy in treating ALL and discuss current and future strategies aiming at reducing their risk.

摘要

急性淋巴细胞白血病(ALL)约占儿童癌症的25%,占成人白血病病例的20%,男性患病率高于女性。其特征为疲劳、发热和骨痛等症状,若不治疗会带来显著的死亡风险。虽然化疗和干细胞移植是标准治疗方法,但在复发或难治性病例中其疗效会下降,这凸显了创新治疗方法的必要性。嵌合抗原受体(CAR)T细胞疗法已成为一种变革性技术,有可能克服这些挑战并实现持久缓解。CAR T细胞疗法具有显著优势,包括靶向特定抗原、克服高危基因突变以及在儿科和成人患者中实现持续缓解。然而,仍存在显著挑战,如细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性综合征(ICANS)。在本综述中,我们聚焦于CAR T细胞疗法治疗ALL时相关的神经症状,并讨论旨在降低其风险的当前和未来策略。

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本文引用的文献

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