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:Phase I CAR-T Clinical Trials Review.
Phase I CAR-T Clinical Trials Review.
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标准化发表标准并提供 I 期临床试验的基本要素对于确保稿件高质量至关重要。随着 CAR-T 细胞疗法的快速发展和高昂成本,应采用基于模型和模型辅助等先进设计,以提高临床试验的效率。
具有肿瘤特异性的嵌合抗原受体(CAR)T细胞正被越来越多地研究。I期试验是测试新型CAR-T 疗法安全性的第一步,以确定最大耐受剂量(MTD)。随着时间推移,已开发出多种剂量递增方法,包括基于规则、基于模型和模型辅助的设计。本项目旨在概述当前CAR-T 试验中使用的I期设计。
我们检索了PubMed,查找2015年1月1日至2021年12月31日期间发表的同行评审文献。检索限于英文的人类研究,使用的关键词为“CAR-T phase I”、“clinical trials”和“full text”。
共纳入109篇至少包含部分I期内容的论文进行分析。31.2%的试验使用了传统的3+3设计或其变体,60.6%未提及剂量递增设计。大多数论文(59.6%)未报告队列规模,而19.3%未说明评估时间。尽管大多数研究已在CT.gov注册,但仅有33.9%向CT.gov提交或发布了任何结果。这些趋势即使在发表于高影响因子期刊的论文中也持续存在。
We searched PubMed for peer-reviewed literature published between January 1, 2015 and December 31, 2021. The search was limited to human studies in the English language using the keywords "CAR-T phase I", "clinical trials", and "full text".
One hundred nine papers with at least partial phase I components were included for analysis. 31.2% of the trials used the traditional 3+3 or a variation of said design, and 60.6% did not mention the dose escalation design. The majority of the manuscripts (59.6%) did not report cohort size while 19.3% did not specify the timing of evaluation. Although most of the studies were registered with CT.gov, only 33.9% had any results submitted or posted to CT.gov These trends persisted even in manuscripts published in journals with high impact factors.
Standardizing the publication criteria and providing basic elements of phase I clinical trials are critical to ensure high quality of manuscripts. With the quick development and high costs of CAR-T cell therapy, adoption of advanced designs such as model-based and model-assisted should increase to improve efficiency of clinical trials.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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