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:Cardiotoxicity Associated With Chimeric Antigen Receptor (CAR)-T Cell Therapy for Hematologic Malignancies: A Systematic Review.
Cardiotoxicity Associated With Chimeric Antigen Receptor (CAR)-T Cell Therapy for Hematologic Malignancies: A Systematic Review.
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。
嵌合抗原受体(CAR)-T 细胞疗法是治疗血液系统恶性肿瘤最重要的突破之一。另一方面,该疗法具有许多毒性。CAR-T 疗法的毒性之一是心脏毒性。本系统综述的目的是阐述与 CAR-T 疗法治疗血液系统恶性肿瘤相关的心脏毒性。本系统综述遵循系统综述和荟萃分析优先报告条目(PRISMA)2020 指南。系统检索使用 PubMed、PubMed Central(PMC)、Google Scholar、Cochrane Library、ScienceDirect 和 ClinicalTrials.gov 完成。检索和研究的筛选分别于 2022 年 4 月 28 日和 2022 年 5 月 6 日完成。研究基于参与者、干预和结局(PIO)要素进行选择,纳入的文章为过去十年内发表的全文文章、临床试验、荟萃分析、随机对照试验、综述和系统综述。排除标准为非血液系统恶性肿瘤、非英语语言文章。初步检索有 2,159 篇出版物。这些出版物使用叙事综述文章评估量表(SANRA)、纽卡斯尔-渥太华量表(NCOS)和 Cochrane 协作偏倚风险工具(CCRBT)等评估工具进行评估,最终选出八篇出版物。本系统综述得出结论,接受 CAR-T 细胞疗法的成人和儿科患者中发生了心脏毒性,且这些心脏不良事件有许多危险因素。因此,监测这些心脏毒性极为必要。
Chimeric Antigen Receptor (CAR)-T cell therapy has been one of the most important breakthroughs for treating hematologic malignancies. On the other hand, the therapy had many toxicities. One of the toxicities of the CAR-T therapy is cardiotoxicity. The goal of the systematic review is to elaborate on the cardiotoxicities related to CAR-T therapy for hematologic malignancies. The systematic review is following the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) 2020 guidelines. The systematic search was done using PubMed, PubMed Central (PMC), Google Scholar, Cochrane Library, ScienceDirect, and clinicaltrial. gov. The search and selection of studies were done on April 28, 2022, and May 6, 2022, respectively.
The studies were selected based upon participants, intervention, and outcomes (PIO) elements and the articles that were included were, full-text articles published within the last ten years, clinical trials, meta-analyses, randomized controlled trial, review, and systematic review. The exclusion criteria were non-hematologic malignancy, non-English-language articles. The initial search had 2,159 publications.
The publications were assessed with assessment tools of Scale of the Assessment of Narrative Review Articles (SANRA), Newcastle-Ottawa Scale (NCOS), and Cochrane Collaboration Risk of Bias Tool (CCRBT), which led to selection of eight publications. The systematic review concludes that cardiotoxicity happened in adults and pediatric patients receiving the CAR-T cell therapy and that those cardiac adverse events had many risk factors.
Therefore, monitoring these cardiotoxicities is highly essential.
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