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:Analysis of short-term clinical efficacy and immune function changes of advanced non-small cell lung cancer after radiotherapy or chemotherapy under CT-guided (125)I seed implantation.
Analysis of short-term clinical efficacy and immune function changes of advanced non-small cell lung cancer after radiotherapy or chemotherapy under CT-guided (125)I seed implantation.
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CT 引导下 125I 粒子治疗可能是对放化疗后进展的 NSCLC 的一种有效治疗方法。局部治疗可改善患者的生活质量并减少肿瘤负荷。CT 引导下 125I 放射性粒子植入可能改善放化疗后复发或进展的 NSCLC 患者的免疫状态,并可能增强抗肿瘤免疫反应。
评估CT引导下125I放射性粒子植入治疗放化疗后疾病进展的晚期非小细胞肺癌(NSCLC)患者的临床疗效、安全性及免疫状态变化。
2016年1月至2022年6月,对34例放化疗后进展的NSCLC患者进行回顾性研究。共有34个可评估病灶,在CT引导下将125 I粒子植入病灶内。研究终点如下:短期临床疗效、生活质量评分和不良反应状态评估,并收集患者进行免疫状态评估。
术后平均随访时间为16.58 ± 7.41个月。术后1年生存率为76.47%(26/34),术后2年生存率为58.82%(20/34),中位总生存期为16(6-24)个月(95% CI:13.7-18.3)。术后1年无进展生存期(PFS)率为61.76%(21/34),2年PFS率为41.18%(14/34),中位PFS为12.5(1-24)个月(95% CI:10.8-16.2)。术后气胸发生率为11.76%,少量出血为5.88%,肺炎为2.94%,经对症治疗后均好转。与术前结果相比,治疗组术后1、2、3、6个月CD3 + 和CD4 + T淋巴细胞百分比升高;术后3、6个月NK细胞百分比升高。术后2、3、6个月IL-2和TNF-α阳性免疫因子水平升高;术后1、2、3、6个月γ-IFN水平升高;术后3、6个月IL-4水平降低;术后6个月IL-10水平降低。术后1、2、3、6个月TH17(IL-17)水平降低。
To evaluate the clinical efficacy, safety, and changes in the immune status of advanced non-small cell lung cancer (NSCLC) patients with disease progression after chemoradiotherapy treated with CT-guided 125 I radioactive seed implantation.
From January 2016 to June 2022, 34 NSCLC patients who progressed after radiotherapy and chemotherapy were studied retrospectively. There were 34 evaluable lesions, and 125 I seeds were implanted into the lesions under CT guidance. The study's endpoints were as follows: short-term clinical efficacy, quality of life score, and adverse reaction status assessment, with patients being collected for immune status assessment.
The average postoperative follow-up period was 16.58 ± 7.41 months. The 1-year postoperative survival rate was 76.47% (26/34), the 2-year postoperative survival rate was 58.82% (20/34), and the median overall survival was 16 (6-24) months (95% CI: 13.7-18.3). The 1-year progression-free survival (PFS) rate after the operation was 61.76% (21/34), the 2-year PFS rate was 41.18% (14/34), and the median PFS was 12.5 (1-24) months (95% CI: 10.8-16.2). Postoperative pneumothorax occurred in 11.76% of patients, minor bleeding in 5.88%, and pneumonia in 2.94%, all of which improved after symptomatic treatment. Compared with the preoperative results, the percentages of CD3 + and CD4 + T lymphocytes in the treatment group increased 1, 2, 3, and 6 months after surgery; the percentage of NK cells increased 3 and 6 months after surgery. The positive immune factor levels of IL-2 and TNF-α were increased at 2, 3, and 6 months after surgery; γ-IFN levels were increased at 1, 2, 3, and 6 months after surgery; IL-4 levels were decreased at 3 and 6 months after surgery; and IL-10 levels were decreased at 6 months after surgery. TH17 (IL-17) levels decreased at 1, 2, 3, and 6 months after surgery.
CT-guided 125 I particle therapy may be an effective treatment for NSCLC that has progressed following radiotherapy and chemotherapy. Local treatments improve patients' quality of life and reduce tumor burden. CT-guided 125 I radioactive seed implantation may improve the immune status of patients with recurrent or progressive NSCLC after radiotherapy and chemotherapy and may enhance the antitumor immune response.
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