Gastrointestinal Research Unit, Mayo Clinic, Rochester.
Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester; Alliance Statistics and Data Management Center, Mayo Clinic, Rochester.
Ann Oncol. 2022 Nov;33(11):1159-1167. doi: 10.1016/j.annonc.2022.07.1942. Epub 2022 Aug 10.
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, N) and high-risk (T and/or N) 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 = 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 < 0.0001), but not left-sided tumors (P = 0.1731). Among clinical low-risk patients, low (versus high) TILs were adversely prognostic only in right-sided tumors (P = 0.0058). Among high-risk patients, low TILs were prognostic independent of sidedness (P < 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.
NCT00079274; https://clinicaltrials.gov/ct2/show/NCT00079274.
肿瘤浸润淋巴细胞(TILs)是局部结肠癌中一个强大且独立的预后变量。鉴于右侧和左侧肿瘤的分子特征和预后存在差异,我们通过 III 期癌症的原发肿瘤侧别(包括临床低危(T、N)和高危(T 和/或 N)组),检查 TIL 密度与患者生存的相关性。
在一项基于 FOLFOX 的辅助化疗的 III 期试验中,根据优化无病生存(DFS)的截断点,分析了 1532 例结肠癌中的 TIL 密度并进行了二分类。右侧肿瘤定义为脾曲近端。使用 Kaplan-Meier 方法以及多变量建模和 Cox 回归的相对贡献分析,检查 TILs 和侧别与 5 年 DFS 的关联。
与右侧肿瘤相比,左侧肿瘤的 TIL 密度较低(P < 0.0001)。TIL 密度与 DFS 的相关性因肿瘤侧别而异(P = 0.045)。总体而言,低 TIL(相对于高 TIL)的患者肿瘤在右侧肿瘤中 DFS 明显较差(风险比 2.02,95%置信区间 1.45-2.82;P < 0.0001),但左侧肿瘤则不然(P = 0.1731)。在临床低危患者中,仅在右侧肿瘤中,低(相对于高)TIL 是不利的预后因素(P = 0.0058)。在高危患者中,TIL 是独立于侧别预测预后的(P < 0.025)。在右侧肿瘤中,TIL 对 DFS 的相对贡献明显大于左侧肿瘤(24%比 1.5%)。在高危肿瘤中,TIL 对 DFS 的相对贡献(42%)是所有变量中最高的。在低危肿瘤中,TIL 对 DFS 的贡献(16%)仅次于 KRAS。
TIL 密度与患者生存的相关性因原发肿瘤侧别和临床风险组而异,这表明在 III 期结肠癌中应在此背景下解读 TILs。
gov 标识符:NCT00079274;https://clinicaltrials.gov/ct2/show/NCT00079274。