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 prognostic impact of tumor mutations and tumor-infiltrating lymphocytes in patients with localized pMMR colorectal cancer - A systematic review and meta-analysis.
The prognostic impact of tumor mutations and tumor-infiltrating lymphocytes in patients with localized pMMR colorectal cancer - A systematic review and meta-analysis.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
TILs 高浸润,尤其是 CD3+ 和 CD8+,与生存期显著改善相关,而 BRAF 和 KRAS 突变则与非转移性 pMMR CRC 患者更差的生存结局相关。
肿瘤突变和肿瘤微环境的组成对结直肠癌(CRC)的预后和治疗具有重要意义。然而,免疫治疗对错配修复功能完整(pMMR)的CRC患者仍是一大挑战。本文探讨了TIL(肿瘤浸润淋巴细胞)(TILs)与肿瘤突变对局限性pMMR CRC患者生存结局的关联。
按照PRISMA指南进行了系统文献综述和meta分析。文献检索在PubMed、Embase、Cochrane Library和Web of Science中进行。关注的结局为总生存期、无病生存期和癌症特异性生存期。通过纽卡斯尔-渥太华量表评估偏倚风险,并通过改良GRADE方法评价累积证据的质量。
共筛选出8498篇符合条件的研究文章,最终纳入44篇进行meta分析,共涉及33,704例患者。任何TILs高浸润的患者均显示总生存期显著改善(HR = 0.57,95 % CI:0.49-0.67,I 2:0 %),尤其是CD3 +(HR = 0.52,95 % CI:0.38-0.71,I 2:0 %)和CD8 +(HR = 0.60,95 % CI:0.37-0.99,I 2:10 %)TILs亚组。BRAF突变(HR = 2.68,95 % CI:1.47-4.89,I 2:83 %)和KRAS突变(HR = 1.25,95 % CI:1.18-1.33,I 2:0 %)的患者总生存期缩短。
Tumor mutations and the composition of the tumor microenvironment have prognostic and therapeutic significance in colorectal cancer (CRC). However, immunotherapy remains a challenge for patients with proficient mismatch repair (pMMR) CRC. In this paper, the association between tumor-infiltrating lymphocytes (TILs) and tumor mutations on survival outcomes in patients with localized pMMR CRC was examined.
A systematic review of the literature and a meta-analysis were conducted in accordance with the PRISMA guidelines. The literature search was conducted in PubMed, Embase, Cochrane Library, and Web of Science. The outcomes of interest were overall survival, disease-free survival, and cancer-specific survival. The risk of bias was assessed through the Newcastle-Ottawa Scale and the quality of the cumulative evidence was evaluated through the modified GRADE approach.
In total, 8498 articles were screened for eligibility and 44 articles were included in the meta-analysis with 33,704 patients in total. Patients with high infiltration of any TILs showed significantly improved overall survival (HR = 0.57, 95 % CI: 0.49-0.67, I 2 : 0 %), especially for the subgroup of CD3 + (HR = 0.52, 95 % CI: 0.38-0.71, I 2 : 0 %) and CD8 + (HR = 0.60, 95 % CI: 0.37-0.99, I 2 : 10 %) TILs. Patients with BRAF mutation (HR = 2.68, 95 % CI: 1.47-4.89, I 2 : 83 %) and KRAS mutation (HR = 1.25, 95 % CI: 1.18-1.33, I 2 : 0 %) showed decreased overall survival. INTERPRETATION: High infiltration of TILs, especially CD3 + and CD8 + , was associated with significantly improved survival, while BRAF and KRAS mutations were correlated with worse survival outcomes for patients with non-metastatic pMMR CRC.
MEMBER ACCOUNT
登录成功会直接打开下一页。