CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Advances in treatments of patients with classical and emergent neurological toxicities of anticancer agents.
Advances in treatments of patients with classical and emergent neurological toxicities of anticancer agents.
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近年来,抗癌治疗相关神经毒性受到越来越多关注。过去20年创新疗法发展带来新的毒性类型,其临床诊断和处理较具挑战,需要进一步研究其发病机制。放疗和化疗可引起已知及新近受到关注的中枢和周围神经系统毒性。通过“从实验室到临床再回到实验室”的研究识别风险因素并理解发病机制,是开发减毒策略的第一步;新型影像技术和生物学检测对诊断也十分重要。免疫治疗使癌症治疗从以肿瘤细胞为中心转向调节免疫以实现有效抗肿瘤反应。免疫检查点抑制剂及CAR-T 增加免疫介导毒性发生率,为神经系统患者管理带来新挑战。ICI相关神经不良事件虽少见但可能严重,可累及中枢和周围神经系统。临床和生物学特征最明确且较常见的是周围神经表型,如肌炎和多发性神经根神经病;中枢表型及其治疗认识也在增加。管理需在抑制自身免疫毒性与不损害抗癌免疫之间取得平衡。CAR-T 等过继细胞疗法可诱发细胞活化和大量促炎细胞因子产生,导致常见且有时严重的CRS和免疫效应细胞相关神经综合征。管理需要肿瘤科/血液科、神经科和重症医学密切协作。癌症患者管理需临床多学科团队及研究团队共同推动神经毒性的理解和处理。
The neurotoxicity associated to the anticancer treatments has received a growing body of interest in the recent years. The development of innovating therapies over the last 20years has led to the emergence of new toxicities. Their diagnosis and management can be challenging in the clinical practice and further research is warranted to improve the understanding of their pathogenic mechanisms. Conventional treatments as radiation therapy and chemotherapy are associated to well-known and under exploration emerging central nervous system (CNS) and peripheral nervous system (PNS) toxicities. The identification of the risk factors and a better understanding of their pathogeny through a "bench to bedside and back again" approach, are the first steps towards the development of toxicity mitigation strategies. New imaging techniques and biological explorations are invaluable for their diagnosis. Immunotherapies have changed the cancer treatment paradigm from tumor cell centered to immune modulation towards an efficient anticancer immune response. The use of the immune checkpoints inhibitors (ICI) and CAR-T cells (chimeric antigen receptor) lead to an increase in the incidence of immune-mediated toxicities and new challenges in the neurological patient's management.
The neurological ICI related adverse events (n-irAE) are rare but potentially severe and may present with both CNS and PNS involvement. The most frequent and well characterized, from a clinical and biological standpoint, are the PNS phenotypes: myositis and polyradiculoneuropathy, but the knowledge on CNS phenotypes and their treatments is expanding. The n-irAE management requires a good balance between dampening the autoimmune toxicity without impairing the anticancer immunity.
The adoptive cell therapies as CAR-T cells, a promising anticancer strategy, trigger cellular activation and massive production of proinflammatory cytokines inducing frequent and sometime severe toxicity known as cytokine release syndrome and immune effector cell-associated neurologic syndrome.
Their management requires a close partnership between oncologist-hematologists, neurologists, and intensivists. The oncological patient's management requires a multidisciplinary clinical team (oncologist, neurologist and paramedical) as well as a research team leading towards a better understanding and a better management of the neurological toxicities.
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