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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A retrospective pharmacovigilance analysis based on the FAERS database reveals sex-associated differences in toxicities of CAR T-cell therapy.
A retrospective pharmacovigilance analysis based on the FAERS database reveals sex-associated differences in toxicities of CAR T-cell therapy.
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嵌合抗原受体(CAR)T细胞疗法显著改善了血液系统恶性肿瘤的治疗结局;然而,治疗相关毒性往往较为严重,且毒性方面与性别相关的差异仍未得到充分研究。在此,我们从FDA不良事件报告系统(FAERS)中提取数据,以评估CAR-T 细胞疗法毒性中与性别相关的差异。在7700例病例中,女性报告细胞因子释放综合征(CRS)的报告比值比更高,报告比值比(ROR)为1.10,置信区间(CI)为[1.00, 1.20],白血病亦然(ROR = 1.34;CI [1.05, 1.70])。在多个器官系统中均观察到女性报告比值比升高。跨癌症治疗的比较表明,CAR-T 细胞疗法中与性别相关的报告模式不能归因于癌症疗法之间的基线性别差异。分层分析进一步识别出按癌症类型和CAR-T 产品划分的异质性。这些结果凸显了与性别相关的独特毒性模式,并可能支持将性别纳入毒性管理。
Chimeric antigen receptor (CAR) T-cell therapy has significantly advanced treatment outcomes for hematological malignancies; however, therapy-associated toxicities are often severe and sex-related differences in toxicity remain under-investigated.
Here, we extract data from FDA Adverse Event Reporting System (FAERS) to evaluate sex-associated differences in CAR T-cell therapy toxicities. Among 7700 cases, females show higher reporting odds of cytokine release syndrome (CRS), with a reporting odds ratio (ROR) of 1. 10 and a confidence interval (CI) of [1. 00, 1. 20], as well as leukemias (ROR = 1. 34; CI [1. 05, 1. 70]). Elevated reporting odds in females are observed across multiple organ systems.
Comparisons across cancer treatments indicate that sex-associated reporting patterns in CAR T-cell therapy cannot be attributed to baseline sex differences across cancer therapies. Stratified analyses further identify heterogeneity by cancer type and CAR T product. These results highlight distinct sex-associated toxicity patterns and may support incorporating sex into toxicity management.
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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