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嵌合抗原受体 T 细胞疗法在肿瘤学中的应用——概览:对 ClinicalTrials.gov 数据库的分析。

Chimeric antigen receptor T cell therapy in oncology - Pipeline at a glance: Analysis of the ClinicalTrials.gov database.

机构信息

Division of Hematology, Mayo Clinic, Scottsdale, United States.

出版信息

Crit Rev Oncol Hematol. 2021 Mar;159:103239. doi: 10.1016/j.critrevonc.2021.103239. Epub 2021 Jan 23.

Abstract

There is a rapid growth of published data associated with chimeric antigen receptor (CAR) T-cells, and its evaluation is becoming challenging. We performed a review of the ClinicalTrials.gov database, searching for clinical trials using CAR T-cell therapy in oncology (cut-off December 2019). 593 trials were found. 48 % of trials are from China and 39 % from the USA. 63 % percent focused on hematologic malignancies, while gastrointestinal cancer, breast cancer, and nervous system were the top 3 solid tumors addressed. Common targets in hematologic malignancies are CD19 and BCMA; while mesothelin and CD171 in solid tumors. Second-generation CAR T designs predominate with CD28 or 41BB co-stimulation. Mixed sponsors supported 45 % of trials, and only 19 % received funding exclusively from industry. Current trends suggest that 900 CAR T-cell therapy clinical trials will be registered during 2020-2025. We estimate a two-fold increase in trials that study allogeneic cell products in the next five years.

摘要

与嵌合抗原受体 (CAR) T 细胞相关的已发表数据呈快速增长趋势,其评估变得具有挑战性。我们对 ClinicalTrials.gov 数据库进行了审查,搜索了 2019 年 12 月截止日期前使用 CAR T 细胞疗法治疗肿瘤的临床试验。共发现 593 项试验。其中 48%来自中国,39%来自美国。63%的试验集中于血液系统恶性肿瘤,而胃肠道癌、乳腺癌和神经系统是治疗的前 3 大实体瘤。血液系统恶性肿瘤中的常见靶点是 CD19 和 BCMA;而实体瘤中的常见靶点是间皮素和 CD171。第二代 CAR T 设计以 CD28 或 41BB 共刺激为主。混合赞助商支持了 45%的试验,只有 19%的试验仅获得了产业的资助。目前的趋势表明,2020 年至 2025 年期间将有 900 项 CAR T 细胞治疗临床试验注册。我们预计,在未来五年内,研究同种异体细胞产品的试验数量将增加一倍。

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