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:Management of Immune-Related Adverse Events in Patients Treated With Chimeric Antigen Receptor T-Cell Therapy: ASCO Guideline.
Management of Immune-Related Adverse Events in Patients Treated With Chimeric Antigen Receptor T-Cell Therapy: ASCO Guideline.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
提高对接受嵌合抗原受体(CAR)T细胞治疗患者免疫相关不良事件(irAEs)推荐管理的认识,概述策略并提供指导。
一个由医学肿瘤学、神经病学、血液学、急诊医学、护理、试验研究人员和倡导专家组成的多学科小组被召集起来制定该指南。指南制定涉及系统性文献回顾和非正式共识过程。系统性回顾侧重于2017年至2021年发表的证据。
系统综述确定了35篇符合条件的出版物。由于缺乏高质量证据,推荐意见基于专家共识。推荐意见:多学科团队发布了推荐意见,以帮助识别、检查、评估和管理最常见的CAR-T 细胞相关毒性,包括细胞因子释放综合征、免疫效应细胞相关神经毒性综合征、B细胞发育不全、血细胞减少和感染。对于大多数患者,CAR-T 细胞相关短期毒性的管理从支持治疗开始,但对于反应不充分的患者,可能需要药物干预。对于持续性或重度CAR-T 细胞相关细胞因子释放综合征患者的管理,包括使用tocilizumab联合或不联合皮质类固醇治疗。基于病情可能快速恶化的可能性,中度至重度免疫效应细胞相关神经毒性综合征患者应接受皮质类固醇和支持治疗。更多信息可在www.asco.org/supportive-care-guidelines获取。
To increase awareness, outline strategies, and offer guidance on the recommended management of immune-related adverse events (irAEs) in patients treated with chimeric antigen receptor (CAR) T-cell therapy.
A multidisciplinary panel of medical oncology, neurology, hematology, emergency medicine, nursing, trialists, and advocacy experts was convened to develop the guideline. Guideline development involved a systematic literature review and an informal consensus process. The systematic review focused on evidence published from 2017 to 2021.
The systematic review identified 35 eligible publications. Because of the paucity of high-quality evidence, recommendations are based on expert consensus. RECOMMENDATIONS: The multidisciplinary team issued recommendations to aid in the recognition, workup, evaluation, and management of the most common CAR T-cell-related toxicities, including cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, B-cell aplasia, cytopenias, and infections. Management of short-term toxicities associated with CAR T cells begins with supportive care for most patients, but may require pharmacologic interventions for those without adequate response. Management of patients with prolonged or severe CAR T-cell-associated cytokine release syndrome includes treatment with tocilizumab with or without a corticosteroid. On the basis of the potential for rapid decline, patients with moderate to severe immune effector cell-associated neurotoxicity syndrome should be managed with corticosteroids and supportive care.Additional information is available at www.asco.org/supportive-care-guidelines.
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