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 depends on primary tumor sidedness in stage III colon cancers (NCCTG N0147) [Alliance].
Association of tumor-infiltrating lymphocytes with survival depends on primary tumor sidedness in stage III colon cancers (NCCTG N0147) [Alliance].
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TIL 密度与患者生存的关联因原发肿瘤侧别和临床风险组而异,提示在 III 期结肠癌中应结合此背景解读 TIL。GOV IDENTIFIER: NCT00079274; https://ClinicalTrials.gov/ct2/show/NCT00079274。
TIL(肿瘤浸润淋巴细胞)(TILs)是局限性结肠癌中一个稳健且独立的预后变量。鉴于右半与左半肿瘤在分子特征和预后方面存在已报道的差异,我们在III期癌症中按原发肿瘤侧别检查了TIL密度与患者生存的关联,包括临床低危(T 1-3,N 1)和高危(T 4 和/或N 2)组。
在一项基于FOLFOX辅助化疗的III期试验中,对结肠癌(N = 1532)的TIL密度进行了分析,并根据先前确定的针对无病生存期(DFS)优化的截点进行二分类。右侧肿瘤定义为位于脾曲近端。采用Kaplan-Meier方法以及多变量建模和Cox回归相对贡献分析,检验了TIL和肿瘤侧别与5年DFS的关联。
左侧肿瘤的TIL密度低于右侧肿瘤(P < 0.0001)。TIL密度与DFS的关联因肿瘤侧别而存在显著差异(P interaction = 0.045)。总体而言,TIL低(相对于高)的患者肿瘤在右侧肿瘤中DFS显著较差(风险比2.02,95%置信区间1.45-2.82;P adj < 0.0001),但在左侧肿瘤中则不然(P adj = 0.1731)。在临床低风险患者中,TIL低(相对于高)仅在右侧肿瘤中具有不良预后意义(P adj = 0.0058)。在高风险患者中,低TIL的预后意义独立于肿瘤侧别(P adj < 0.025)。TIL对DFS的相对贡献在右侧肿瘤中显著大于左侧肿瘤(24%对1.5%)。在高风险肿瘤中,TIL对所有变量中DFS的相对贡献最高(42%)。在低风险肿瘤中,TIL对DFS的贡献(16%)仅次于KRAS。
Tumor-infiltrating lymphocytes (TILs) are a robust and independent prognostic variable in localized colon cancer. Given reported differences in molecular features and prognosis of right- versus left-sided tumors, we examined the association of TIL densities with patient survival by primary tumor sidedness in stage III cancers, including clinical low- (T 1-3 , N 1 ) and high-risk (T 4 and/or N 2 ) groups.
In a phase III trial of FOLFOX-based adjuvant chemotherapy, TIL densities were analyzed and dichotomized in colon carcinomas (N = 1532) based on a previously determined cut point optimized for disease-free survival (DFS). Right-sided tumors were defined as proximal to the splenic flexure. Associations of TILs and sidedness with 5-year DFS were examined using Kaplan-Meier methodology along with multivariable modeling and relative contribution analysis by Cox regression.
Lower TIL densities were found in left- versus right-sided tumors (P < 0.0001). The association of TIL densities with DFS differed significantly by tumor sidedness (P interaction = 0.045). Overall, patient tumors with low (versus high) TILs had significantly poorer DFS in right-sided (hazard ratio 2.02, 95% confidence interval 1.45-2.82; P adj < 0.0001), but not left-sided tumors (P adj = 0.1731). Among clinical low-risk patients, low (versus high) TILs were adversely prognostic only in right-sided tumors (P adj = 0.0058). Among high-risk patients, low TILs were prognostic independent of sidedness (P adj < 0.025). The relative contribution of TILs to DFS was substantially greater in right- versus left-sided tumors (24% versus 1.5%). In high-risk tumors, TILs had the highest relative contribution to DFS (42%) of all variables. In low-risk tumors, the contribution of TILs (16%) to DFS was second to KRAS.
The association of TIL densities with patient survival differed by primary tumor sidedness and clinical risk group, suggesting that TILs should be interpreted in this context among stage III colon cancers. GOV IDENTIFIER: NCT00079274; https://clinicaltrials.gov/ct2/show/NCT00079274.
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