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:Nursing care of patients with relapsed and refractory multiple myeloma treated with B-cell mature antigen-targeted universal chimeric antigen receptor T cells.
Nursing care of patients with relapsed and refractory multiple myeloma treated with B-cell mature antigen-targeted universal chimeric antigen receptor T cells.
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探讨使用B细胞成熟抗原(BCMA)靶向通用型CAR-T 细胞(BCMA-UCART)免疫疗法治疗8例复发难治性多发性骨髓瘤(MM)患者的护理方法疗效。
本研究选取2020年5月至2022年11月在我科接受BCMA靶向UCART治疗的16例复发难治性MM患者,根据护理方法的不同分为对照组和实验组,每组8例,对照组采用常规通用护理方案。实验组采用配合本研究的免疫治疗的护理方案,护理要点包括及时评估器官功能状态,安全准确地输注BCMA-UCART,识别和处理BCMA-UCART输注后细胞因子释放引起的高热、低血压、心律失常和中枢神经系统不良反应,以及管理液体失衡、维持血压稳定、配合医生有效控制炎症因子。
此外,为患者提供心理和饮食支持。比较两组干预后住院时间。实验组出院时间明显短于对照组(P<0.05),实验组有效控制了细胞因子释放综合征、免疫效应细胞相关神经毒性综合征和急性移植物抗宿主病。BCMA-UCART免疫治疗的护理方案对MM患者干预有效,促进其早期康复和出院。
To investigate the efficacy of a nursing approach using B-cell maturation antigen (BCMA)-targeted universal chimeric antigen receptor T-cell (BCMA-UCART) immunotherapy in the treatment of 8 patients with relapsed refractory multiple myeloma (MM). In this study, 16 patients with relapsed and refractory MM who were treated with BCMA-targeted UCART in our department from May 2020 to November 2022 were selected, and were divided into a control group and an experimental group of 8 cases each according to the difference in the nursing methods, and the control group adopted the conventional universal nursing program.
The experimental group used the nursing protocol that cooperated with the immunotherapy of this study, and the main points of nursing care included timely assessment of organ functional status, safe and accurate infusion of BCMA-UCART, identification and management of hyperthermia, hypotension, arrhythmia and central nervous system adverse reactions caused by cytokine release after BCMA-UCART infusion, as well as management of fluid imbalance, maintenance of stable blood pressure, and cooperation with physicians to effectively control of inflammatory factors.
In addition, patients were provided with psychological and dietary support. The duration of hospitalization was compared between the two groups after the intervention. The discharge time of the experimental group was significantly shorter than that of the control group (P he.
05), and the experimental group effectively controlled cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome and acute graft-versus-host disease. The nursing program with BCMA-UCART immunotherapy is effective in intervening MM patients and promotes their early recovery and discharge from the hospital.
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