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:Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence.
Cancer-related cognitive impairment in patients with hematologic malignancies after CAR T cell therapy: a systematic review and meta-analysis of prevalence.
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这些发现强调了制定针对性干预措施以在短期和长期随访期间预防或管理癌症患者认知障碍的重要性。
癌症相关认知障碍是接受嵌合抗原受体(CAR)T 细胞治疗患者神经毒性的表现之一。目前缺乏对血液系统恶性肿瘤患者 CAR-T 治疗后短期和长期随访中癌症相关认知障碍总体患病率的估计。本综述旨在总结患者认知功能状况,并估算 CAR-T 治疗后不足 1 个月、1–12 个月和超过 12 个月随访时癌症相关认知障碍的患病率。
检索自建库至 2024 年 8 月的 PubMed、Cochrane Library、EMBASE、CINAHL Plus、Web of Science,以及通过 ProQuest 获取的 PsycINFO。纳入采用有效测量工具报告 CAR-T 治疗患者认知障碍的研究。使用随机效应模型合并认知障碍患病率数据。
共纳入 16 项研究,涉及 1,407 例患者。基于神经心理测验评估,三个随访时点(<1 个月、1–12 个月、>12 个月)的癌症相关认知障碍合并患病率分别为 24%[95% 预测区间(PI)16%–33%]、33%(95% PI 9%–64%)和 35%(95% PI 23%–48%)。使用其他测量方式得到的患病率估计值在各随访时点介于 4%–38%。逐一排除研究的荟萃分析量化了潜在离群值对总体患病率估计的影响。
研究结果强调,应开发针对性干预措施,以预防或管理癌症患者短期及长期随访期间的认知障碍。本综述还指出,需要进一步研究该领域,以增进对疾病机制的认识并实施预防策略,管理癌症相关认知障碍。
Cancer-related cognitive impairment is one of the symptoms of neurotoxicity among patients receiving chimeric antigen receptor (CAR) T cell therapy. Evidence of the overall estimated prevalence of cancer-related cognitive impairment following CAR T-cell therapy among patients with hematologic malignancies at short-term and long-term follow-ups is lacking. This review aimed to summarize the cognitive functioning status and estimate the prevalence of cancer-related cognitive impairment at follow-up within 1 month, 1 to 12 months, and > 12 months after CAR T cell therapy.
PubMed, Cochrane Library, EMBASE, CINAHL Plus, Web of Science, and PsycINFO via ProQuest from inception through August 2024. Studies that reported on cognitive impairment among patients receiving CAR T cell therapy with valid measures were included. Data on cognitive impairment prevalence were pooled using a random-effects model.
In total, 16 studies involving 1407 patients were included. The pooled cancer-related cognitive impairment prevalence rates assessed using neuropsychological tests at the follow-up timepoints (< 1 month, 1-12 months, and > 12 months) were 24% [95% prediction interval (PI) 16-33%], 33% (95%, PI 9-64%), and 35% (95%, PI 23-48%), respectively. The prevalence estimates assessed using other measures were ranging from 4 to 38% across different timepoints. The leave-one-out meta-analyses quantified the impact of these potential outliers on the estimation of the overall prevalence.
The findings stress the importance of developing targeted interventions to prevent or manage cognitive impairment in cancer patients during both short-term and long-term follow-up periods. This review also highlights the need for further research in this area to improve our understanding of the disease mechanisms and implement preventive strategies for managing cancer-related cognitive impairment.
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