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:Prognostic value of immunosuppression scores in patients with esophageal squamous cell carcinoma: a multicenter study.
Prognostic value of immunosuppression scores in patients with esophageal squamous cell carcinoma: a multicenter study.
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不同 ISS 状态的 ESCC 代表两种不同的生物学亚型,凸显了针对不同肿瘤行为制定个体化治疗策略的必要性。
研究了人类白细胞抗原-E(HLA-E)表达和自然杀伤(NK)细胞比例在食管鳞状细胞癌(ESCC)中的预后影响。
本研究回顾性评估了两个中心的397例ESCC患者。分析了各组中累积复发率(CIR)和肿瘤相关死亡发生率(CID)。基于HLA-E表达和NK细胞比例开发了免疫抑制评分(ISS)。使用逆概率治疗加权(IPTW)调整组间差异。还检查了影响癌症特异性生存期(CSS)和无复发生存期(RFS)的因素。
HLA-E低表达患者的五年CIR和CID显著高于高表达患者(CIR:20.7% vs. 45.1%,CID:19.3% vs. 40.1%;p < 0.001)。同样,NK细胞阳性患者的五年CIR和CID显著优于NK细胞阴性患者(CIR:16.3% vs. 59.6%,CID:13.9% vs. 53.7%;p < 0.001)。桑基图显示,低ISS组的复发率和肿瘤相关死亡率较低(p < 0.05)。经过IPTW调整后,与高ISS组相比,低ISS组显示出改善的五年RFS(80.1% vs. 35.4%,p < 0.001)和五年CSS(82.3% vs. 42.5%,p < 0.001)。
This study retrospectively evaluated 397 ESCC patients across two centers. The cumulative incidence of recurrence (CIR) and the incidence of tumor-related death (CID) were analyzed in various groups. An immunosuppression score (ISS) was developed based on HLA-E expression and NK cell proportion. Differences between groups were adjusted using inverse probability treatment weighting (IPTW). The factors influencing cancer-specific survival (CSS) and recurrence-free survival (RFS) were also examined.
Patients with low HLA-E expression had significantly higher five-year CIR and CID compared to those with high expression (CIR: 20.7% vs. 45.1%, CID: 19.3% vs. 40.1%; p < 0.001). Similarly, NK cell-positive patients had significantly better five-year CIR and CID than NK cell-negative patients (CIR: 16.3% vs. 59.6%, CID: 13.9% vs. 53.7%; p < 0.001). The Sankey diagram indicated that the low ISS group had a lower recurrence and tumor-related mortality rate ( p < 0.05). After IPTW adjustment, the low ISS group showed improved five-year RFS (80.1% vs. 35.4%, p < 0.001) and five-year CSS (82.3% vs. 42.5%, p < 0.001) compared to the high ISS group.
ESCC with different ISS statuses represents two distinct biological subtypes, underscoring the need for personalized treatment strategies tailored to varying tumor behaviors.
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