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:Managing therapy-associated neurotoxicity in children with ALL.
Managing therapy-associated neurotoxicity in children with ALL.
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多种化疗药物和新型免疫疗法可有效控制全身及中枢神经系统(CNS)白血病,但可能具有显著神经毒性。甲氨蝶呤亚急性神经毒性的表现多样,需要密切管理;不过,几乎所有患者的症状都是短暂的。甲氨蝶呤是预防CNS复发的重要药物,因此神经功能完全恢复后,应争取恢复使用。多数儿童再次接受甲氨蝶呤治疗时耐受良好,不会出现明显延迟或需要预防性用药。CD19嵌合抗原受体(CAR)T细胞和贝林妥欧单抗等新型免疫疗法导致神经毒性的频率更高。现已制定免疫效应细胞相关神经毒性综合征(ICANS)的统一分级系统,并建立基于严重程度的管理流程。低级别ICANS通常经支持治疗后数日内缓解;重度ICANS则需多专科团队在重症监护病房照护,以应对危及生命的癫痫发作和脑水肿。药物干预包括控制癫痫的抗惊厥药及减轻神经炎症的糖皮质激素。针对ICANS病理生理机制的抗细胞因子治疗正在研发中。本文结合典型病例讨论甲氨蝶呤、CAR-T 细胞和贝林妥欧单抗相关神经毒性的管理。
Several chemotherapeutic agents and novel immunotherapies provide excellent control of systemic and central nervous system (CNS) leukemia but can be highly neurotoxic. The manifestations of subacute methotrexate neurotoxicity are diverse and require vigilant management; nonetheless, symptoms are transient in almost all patients. As methotrexate is a crucial drug to prevent CNS relapse, it is important to aim to resume it after full neurologic recovery. Most children tolerate methotrexate rechallenge without significant delays or prophylactic medications. Neurotoxicity is more frequent with newer immunotherapies such as CD19- chimeric antigen receptor T (CAR T) cells and blinatumomab.
A uniform grading system for immune effector cell-associated neurotoxicity syndrome (ICANS) and algorithms for management based on severity have been developed. Low-grade ICANS usually resolves within a few days with supportive measures, but severe ICANS requires multispecialty care in the intensive care unit for life-threatening seizures and cerebral edema.
Pharmacologic interventions include anticonvulsants for seizure control and glucocorticoids to reduce neuroinflammation. Anticytokine therapies targeted to the pathophysiology of ICANS are in development. By using illustrative patient cases, we discuss the management of neurotoxicity from methotrexate, CAR T cells, and blinatumomab in this review.
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