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:Association of Tumor-Infiltrating Lymphocytes With Survival in Stages II and III Colorectal Cancer.
Association of Tumor-Infiltrating Lymphocytes With Survival in Stages II and III Colorectal Cancer.
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肿瘤微环境在肿瘤发生、治疗反应和肿瘤细胞清除中至关重要。TIL(肿瘤浸润淋巴细胞)(TILs)促进宿主免疫反应,并与结直肠癌(CRC)较好的预后相关。这项多中心回顾性研究评估了TILs的存在和强度与生存结局之间的关系。
本研究共纳入651例患者,来自四个葡萄牙肿瘤中心,在2016年至2019年间因II期或III期结直肠腺癌接受手术切除。研究人群的平均年龄为70岁;58.2%为男性。中位总生存期为58.03 ± 1.29个月(95% CI 55.50 - 60.56),中位无病生存期(DFS)为53.02 ± 1.39个月(95% CI 50.29 - 55.74)。高浸润患者(包括中度、大量或克罗恩样浸润)的DFS显著更长,即58.48 ± 1.84个月(95% CI 54.87 - 62.09个月),而无浸润或轻微浸润组为49.22 ± 1.75个月(95% CI 45.79 - 52.64个月);p = 0.003。评估肿瘤侧别时,高浸润与更高的DFS相关(59.86 ± 2.36个月(95% CI 55.23 - 64.50个月)vs 49.60 ± 2.40个月(95% CI 44.90 - 54.29个月),p = 0.011)。这项工作强化了研究CRC患者可能的预后和预测因素的重要性。
The tumor microenvironment is crucial in tumourigenesis, response to therapy, and elimination of tumor cells. Tumor-infiltrating lymphocytes (TILs) promote the host immune response and are associated with a better prognosis in colorectal cancer (CRC). This multicentric retrospective study evaluated the relationship between the presence and intensity of TILs and survival outcomes. A total of 651 patients from four Portuguese oncological centers who underwent surgical resection for stages II or III colorectal adenocarcinoma between 2016 and 2019 were included in this study. The mean age of the study population was 70 years; 58. 2% were males. The median overall survival was 58. 03 ± 1. 29 months (95% confidence interval (CI) 55.
50 - 60. 56), and the median disease-free survival (DFS) was 53. 02 ± 1. 39 months (95% CI 50. 29 - 55. 74). Patients with high infiltrate (including those with moderate, abundant, or Crohn-like infiltrate) had significantly longer DFS i. e. , 58. 48 ± 1. 84 months (95% CI 54. 87 - 62. 09 months) vs 49. 22 ± 1. 75 months (95% CI 45. 79 - 52.
64 months) in the group with absent or minimal infiltrate; p = 0. 003. Assessing the side of the tumor, high infiltrate was associated with higher DFS (59. 86 ± 2. 36 months (95% CI 55. 23 - 64. 50 months) vs 49. 60 ± 2. 40 months (95% CI 44. 90 - 54. 29 months), p = 0. 011). This work reinforces the importance of research into possible prognostic and predictive factors in patients with CRC.
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