← 返回

商业化 CAR-T 细胞治疗后的第二原发恶性肿瘤:FDA 不良事件报告系统分析

英文原题:Second primary malignancies after commercial CAR T-cell therapy: analysis of the FDA Adverse Events Reporting System.

查看英文原题

Second primary malignancies after commercial CAR T-cell therapy: analysis of the FDA Adverse Events Reporting System.

PubMed 2024/05/16(内容时间) Blood Q1 · IF 23.9(JCR 2025)

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。

中文摘要

在食品药品监督管理局不良事件报告系统中,12 394份CAR-T 细胞疗法后的不良事件报告中,有536份(4.3%)报告了第二原发恶性肿瘤。髓系和T细胞肿瘤的报告频率不成比例地更高,值得进一步随访。

展开英文摘要原文

Second primary malignancies were reported in 536 of 12 394 (4.3%) adverse event reports following chimeric antigen receptor T-cell therapies in the Food and Drug Administration Adverse Event Reporting System. Myeloid and T-cell neoplasms were disproportionately more frequently reported, warranting further follow-up.

论文信息

作者
Elsallab M、Ellithi M、Lunning MA、D'Angelo C、Ma J、Perales MA、Frigault M、Maus MV
第一作者单位
Harvard-MIT Center for Regulatory Science, Harvard Medical School, Boston, MA.United States
通讯作者单位
Cellular Immunotherapy Program, Mass General Cancer Center, and Department of Medicine, Harvard Medical School, Boston, MA.United States
文献类型
读者来信
期刊
Blood2024 May 16
原文标识
PubMed 38483155 · DOI 10.1182/blood.2024024166