一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Combined Clinical Efficacy and Safety Analysis of Adoptive Immunotherapy with Radiotherapy and Chemotherapy in Non-Small-Cell Lung Cancer: Systematic Review and Meta-Analysis.
The Combined Clinical Efficacy and Safety Analysis of Adoptive Immunotherapy with Radiotherapy and Chemotherapy in Non-Small-Cell Lung Cancer: Systematic Review and Meta-Analysis.
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过继性免疫治疗联合微放射治疗可降低 NSCLC 的复发并提高患者生存率,且早期患者可从免疫治疗中获益更显著。
探讨放化疗联合过继性免疫治疗与单纯放化疗在非小细胞肺癌(NSCLC)患者中的疗效差异。
合格的随机对照试验(randomized controlled trial,RCT)或非随机同期对照试验(NRCCT),发表于PubMed、EMBASE、中国期刊全文数据库、Medline、Cochrane数据库和维普中文数据库等多个数据库,并采用Revman5.0软件进行数据分析。
我们发现实验组和对照组之间的疗效有显著差异(OR = 1.94,95% CI(1.46,2.58),P < 0.001,I 2 = 0%,Z = 4.59),过继性免疫治疗对疾病进展的影响(OR = 1.80,95% CI(1.38,2.35),P < 0.001,I 2 = 0%,Z = 4.33),过继性免疫治疗对总生存期的影响(OR = 2.19,95% CI(1.60,2.99),P < 0.001,I 2 = 0%,Z = 4.91),以及过继性免疫治疗的不良反应(OR = 1.76,95% CI(1.25,2.48),P = 0.001,I 2 = 0%,Z = 3.26)。
To explore the differential efficacy of chemoradiotherapy combined with adoptive immunotherapy and radiochemotherapy alone in patients with non-small-cell lung cancer (NSCLC).
Qualified randomized controlled trial (randomized controlled trial, RCT), or nonrandomized concurrent controlled trial (NRCCT), published in various databases, including PubMed, EMBASE, Chinese journal full-text database, Medline, Cochrane database, and VIP Chinese database, and the Revman5. 0 software performed the data analysis.
We found the significantly different curative effect between the experimental and control groups (OR = 1.94, 95% CI (1.46, 2.58), P < 0.001, I 2 = 0%, Z = 4.59), effect of adoptive immunotherapy on the progression of disease (OR = 1.80, 95% CI (1.38, 2.35), P < 0.001, I 2 = 0%, Z = 4.33), adoptive immunotherapy on overall survival (OR = 2.19, 95% CI (1.60, 2.99), P < 0.001, I 2 = 0%, Z = 4.91), and adverse effects of adoptive immunotherapy (OR = 1.76, 95% CI (1.25, 2.48), P = 0.001, I 2 = 0%, Z = 3.26).
Adoptive immunotherapy combined with microradiotherapy can decrease the recurrence of NSCLC and improve patient survival, as well as early patients can be benefited more significantly from immunotherapy.
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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