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:Efficacy of DC-CIK Immunotherapy Combined with Chemotherapy on Locally Advanced Gastric Cancer.
Efficacy of DC-CIK Immunotherapy Combined with Chemotherapy on Locally Advanced Gastric Cancer.
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本研究旨在探讨树突状细胞-细胞因子诱导的杀伤细胞(DC-CIK)免疫治疗联合化疗治疗局部晚期胃癌(LAGC)的疗效和安全性。在106例LAGC患者中,53例接受奥沙利铂-5-氟尿嘧啶化疗(对照组),其余53例接受DC-CIK免疫治疗联合化疗(DC-CIK组)。分析短期疗效及免疫功能指标(分化簇(CD)3+、CD4+、CD8+、CD4+/CD8+和自然杀伤(NK)细胞)的变化。DC-CIK组和对照组的总体缓解率(ORR)分别为47.2%(25/53)和41.5%(22/53),疾病控制率(DCR)分别为69.8%(37/53)和50.9%(27/53)。
可以看出,两组之间ORR无统计学显著差异,而DC-CIK组的DCR显著优于对照组。治疗后,与对照组相比,DC-CIK组CD3+ T淋巴细胞、CD4+ T淋巴细胞、CD4+/CD8+细胞和NK细胞的比例明显升高,而CD8+ T淋巴细胞的比例明显下降。治疗后,DC-CIK组QLQ-C30量表功能模块评分显著高于对照组,而症状模块中食欲减退、便秘、呼吸困难、疲乏、疼痛和睡眠障碍评分显著低于对照组。DC-CIK组和对照组的中位生存时间分别为23.4个月和18.6个月。log-rank检验结果显示,DC-CIK组的OS显著优于对照组。DC-CIK免疫治疗联合化疗可改善LAGC患者的免疫细胞功能,提高生活质量,延长生存时间,且不良反应较少。
The aim of the study is to explore the efficacy and safety of dendritic cell-cytokine-induced killer cell (DC-CIK) immunotherapy combined with chemotherapy in the treatment of locally advanced gastric cancer (LAGC). Among 106 patients with LAGC, 53 received the treatment of oxaliplatin-5-fluorouracil chemotherapy (control group), while the remaining 53 received DC-CIK immunotherapy combined with chemotherapy (DC-CIK group). The short-term efficacy and the changes in immune function indexes (cluster of differentiation (CD)3 + , CD4 + , CD8 + , CD4 + /CD8 + , and natural killer (NK) cells) were analyzed. The overall response rate (ORR) was 47. 2% (25/53) and 41. 5% (22/53), and the disease control rate (DCR) was 69. 8% (37/53) and 50. 9% (27/53), respectively, in the DC-CIK group and the control group. It could be seen that the ORR had no statistically significant difference between the two groups, while the DCR in the DC-CIK group was significantly better than that in the control group.
After treatment, the proportions of CD3 + T lymphocytes, CD4 + T lymphocytes, CD4 + /CD8 + cells, and NK cells obviously rose, while the proportion of CD8 + T lymphocytes obviously declined in the DC-CIK group compared with those in the control group. After treatment, the scores in the function module of the QLQ-C30 scale were greatly higher in the DC-CIK group than those in the control group, while the scores of loss of appetite, constipation, dyspnea, fatigue, pain, and sleep disorders in the symptom module were significantly lower in the DC-CIK group than those in the control group.
The median survival time was 23. 4 months and 18. 6 months, respectively, in the DC-CIK group and the control group. The results of the log-rank test showed that the OS in the DC-CIK group was remarkably superior to that in the control group. DC-CIK immunotherapy combined with chemotherapy can improve the immune cell function, ameliorate the quality of life, and prolong the survival time of LAGC patients, with fewer adverse reactions.
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