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 Effect of PD-1 Inhibitor Combined with Chemotherapy on the Level of Peripheral Blood T Lymphocytes among Patients with Non-Small-Cell Lung Cancer and Its Relationship with Prognosis.
The Effect of PD-1 Inhibitor Combined with Chemotherapy on the Level of Peripheral Blood T Lymphocytes among Patients with Non-Small-Cell Lung Cancer and Its Relationship with Prognosis.
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对于 NSCLC 患者,在化疗基础上给予 PD-1 抑制剂可以在保证治疗安全性的前提下,进一步提高临床疗效,改善患者的免疫功能及长期生存率,值得在临床中推广。
探讨PD-1抑制剂联合化疗对非小细胞肺癌(NSCLC)患者外周血T淋巴细胞水平的影响及其与预后的关系。
对2018年6月至2020年9月在广西医科大学附属肿瘤医院接受治疗的150例NSCLC患者进行回顾性分析,其中77例接受PD-1抑制剂联合化疗的患者作为观察组(OG),73例单纯化疗的患者作为对照组(CG)。观察并比较两组的治疗效果、免疫功能指标、血清肿瘤标志物、住院期间不良反应发生率、1年生存率及治疗6个月后的生活质量。
与CG相比,OG的治疗效果明显更好。治疗6个月后,两组CD4+/CD8+、NK细胞及CD4+水平均显著升高,且OG各项指标明显且相对高于另一组。治疗后,与CG相比,OG中CYFRA21-1、CEA和CA125水平显著下降;两组不良反应发生率无显著差异,但OG的1年生存率和6个月生活质量均优于CG。
To explore the effect of combined treatment of PD-1 inhibitor and chemotherapy on the level of peripheral blood T lymphocytes in non-small-cell lung cancer (NSCLC) patients and its relationship with prognosis.
Retrospective analysis was conducted on 150 NSCLC patients treated in Guangxi Medical University Affiliated Tumor Hospital from June 2018 to September 2020, including 77 patients treated with PD-1 inhibitor combined with chemotherapy as the observation group (OG) and 73 patients with chemotherapy alone as the control group (CG). Therapeutic efficacy, immune function indexes, serum tumor markers, incidence of adverse reactions during hospitalization, 1-year survival rate, and life quality after 6 months of treatment were observed and compared between two groups.
Compared to the CG, the therapeutic effect of OG was evidently better. Six months after treatment, levels of CD4 + /CD8 + , NK cells, and CD4 + in two groups were elevated markedly, and indexes of OG were notably and comparatively higher than those in the other group. After treatment, OG was observed with a marked decline regarding levels of CYFRA21-1, CEA, and CA125 compared to those in the CG; and there was no notable difference in terms of adverse reaction occurrence between two groups, but the 1-year survival rate and 6-month life quality in OG over ranked those in CG.
For NSCLC patients, the PD-1 inhibitor given on the basis of chemotherapy can further improve the clinical efficacy and improve immune function and long-term survival rate of patients on the premise of ensuring the safety of treatment, which is worth promoting in clinical practice.
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