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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunotherapy Associated Neurotoxicity in Pediatric Oncology.
Immunotherapy Associated Neurotoxicity in Pediatric Oncology.
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新型免疫疗法在儿童肿瘤学中的应用日益增多,既用于一线治疗,也用于复发/难治性治疗。通过多种作用机制,免疫系统的参与和激活可引起全身性及疾病部位特异性炎症,导致免疫相关不良事件(irAEs)。其中最令人担忧的irAEs之一是神经毒性。其可表现为广泛的神经毒性谱,包括意识模糊、失语、神经病、癫痫发作和/或死亡,起病时间和严重程度各异。早期识别和治疗,通常使用皮质类固醇,仍是神经毒性管理的主要手段,以优化患者预后。神经毒性的病理生理机制因不同治疗策略而异,在大多数情况下仍有待阐明。此外,关于长期神经系统后遗症的了解甚少。本综述将聚焦于儿童肿瘤学中最常用免疫疗法所见的神经毒性,包括CAR-T 细胞疗法、其他形式的过继性细胞疗法、抗体疗法、免疫检查点抑制剂和肿瘤疫苗。本文将讨论免疫治疗相关神经毒性的发生率、病理生理机制、症状学、诊断及目前采用的管理策略,并重点关注儿科特有的考量。
Novel immunotherapies are increasingly being employed in pediatric oncology, both in the upfront and relapsed/refractory settings. Through various mechanisms of action, engagement and activation of the immune system can cause both generalized and disease site-specific inflammation, leading to immune-related adverse events (irAEs). One of the most worrisome irAEs is that of neurotoxicity.
This can present as a large spectrum of neurological toxicities, including confusion, aphasia, neuropathies, seizures, and/or death, with variable onset and severity. Earlier identification and treatment, generally with corticosteroids, remains the mainstay of neurotoxicity management to optimize patient outcomes. The pathophysiology of neurotoxicity varies across the different therapeutic strategies and remains to be elucidated in most cases.
Furthermore, little is known about long-term neurologic sequelae. This review will focus on neurotoxicity seen with the most common immunotherapies used in pediatric oncology, including CAR T cell therapy, alternative forms of adoptive cell therapy, antibody therapies, immune checkpoint inhibitors, and tumor vaccines.
Herein we will discuss the incidence, pathophysiology, symptomatology, diagnosis, and management strategies currently being utilized for immunotherapy-associated neurotoxicity with a focus on pediatric specific considerations.
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