RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Efficiency and Safety of Triple-Drug Combination of Albumin-Bound Paclitaxel, Anlotinib and PD-1/L1 Inhibitors in the 2(nd) or Above Line of Advanced NSCLC: A Retrospective Cohort Study.
The Efficiency and Safety of Triple-Drug Combination of Albumin-Bound Paclitaxel, Anlotinib and PD-1/L1 Inhibitors in the 2(nd) or Above Line of Advanced NSCLC: A Retrospective Cohort Study.
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。
现有研究显示,白蛋白结合型紫杉醇(nab-PTX)、安罗替尼及PD-1/PD-L1抑制剂各自用于晚期非小细胞肺癌(NSCLC)二线及后续治疗均有疗效。本研究通过联合这三种药物,考察优化方案的潜力及其疗效和安全性。
收集2020年1月至2022年1月期间接受过治疗的晚期NSCLC患者资料;这些患者在二线或后续治疗中接受nab-PTX、安罗替尼及PD-1/PD-L1抑制剂联合治疗。主要终点包括客观缓解率(ORR)、无进展生存期(PFS)、疾病控制率(DCR)和总生存期(OS),并记录不良事件(AE)。
该方案在经治NSCLC患者中的ORR为35.71%,平均PFS为5.0个月,平均OS为10.0个月。进一步分析提示,方案疗效与PD-L1表达水平、某些类型不良事件的发生以及NK细胞活性状态等因素有关。此外,该方案毒性可耐受,显示其用于经治晚期NSCLC的潜在适用性。
nab-PTX、安罗替尼及PD-1/PD-L1抑制剂三药联合用于晚期NSCLC二线及以上治疗显示出有希望的疗效,细胞毒性可耐受,提示该方案可能成为重要的二线治疗选择。然而,受患者数量限制,其实际临床价值仍需进一步研究确认。
Existing research data indicates that albumin-bound paclitaxel (nab-ptx), anlotinib, and PD-1/L1 inhibitors have individually shown efficacy in second-line and subsequent treatments for advanced non-small cell lung cancer (NSCLC). This study seeks to investigate the potential of an optimized treatment regimen in this context by combining these three drugs and evaluating both efficacy and safety outcomes.
Between January 2020 and January 2022, we collected data from pre-treated advanced NSCLC patients who received a combination therapy of nab-ptx, anlotinib, and PD-1/L1 inhibitors as a second-line or later treatment. The primary endpoints for the study included the objective response rate (ORR), progression-free survival (PFS), disease control rate (DCR) and overall survival (OS), while adverse events (AEs) were also recorded.
Our findings revealed that the ORR of this regimen in pretreated NSCLC patients was 35.71%, with mean PFS of 5.0 months and mean OS of 10.0 months. Further analysis suggested correlations between the efficacy of the regimen and factors such as PD-L1 expression levels, the occurrence of certain types of adverse events, and the status of NK cell activity. Additionally, the tolerable toxicity profile of this regimen indicates its potential applicability in the treatment of pretreated advanced NSCLC.
Our study displayed that triple-drug combination of nab-ptx, anlotinib and PD-1/L1 inhibitors showed promising efficiency and tolerated cytotoxicity in the 2 nd or above line treatment of advanced NSCLC, indicating the potential of such regimen as an important option for second-line treatment of advanced NSCLC. However, due to limitations in patient numbers, its actual clinical value awaits further research confirmation.
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