Department of Colorectal Surgery and Oncology, Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, People's Republic of China.
Department of Medical Oncology, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, People's Republic of China.
Oncoimmunology. 2021 Mar 22;10(1):1901464. doi: 10.1080/2162402X.2021.1901464.
Immunoscore can accurately predict the prognosis of patients with stage I-III colorectal cancer. However, whether it can be used to predict the prognosis of colorectal cancer peritoneal metastases (CRCPM) remains to be validated. We analyzed peritoneal and ovarian metastases in 68 patients with CRCPM. The immunoscore (IS) was based on the infiltration level of CD3+ and CD8+ T cells, whereas the TBM score was derived from the infiltration level of CD3+, CD8+, CD20+ and CD163+ cells to tumor microenvironment (TME). The predictive value of IS and TBM scores for relapse-free survival (RFS) and overall survival (OS) of patients with CRCPM was analyzed using Kaplan Meier curve and Cox multivariate models. Significant difference in the infiltration levels of different immune cell subtypes in primary lesions, peritoneal metastasis and ovarian metastasis were compared using t-test.CRCPM patients with high IS (>1), high TBM1 score (≥2) or high TBM2 score (≥2) had a significantly longer OS (IS: median OS, not reached vs 23 months, = .0078; TBM1: not reached vs 21.5 months, = .013; TBM2: 39.3 months vs 15.2 months, = .001). On the other hand, patients with high IS had a trend of improved RFS (13.4 months vs 11.0 months, = .067). However, TBM1 and TBM2 score has no predictive utility for RFS. Multivariate analysis revealed that IS, TBM1 and TBM2 can accurately predict OS, but not RFS. Finally, the infiltration level of CD3+ T cells, CD8+ T cells, CD20+ B cells, and CD68+ macrophage was significantly higher in peritoneal metastatic tissue and ovarian metastatic tissue, relative to primary tumor tissues.The IS and TBM score of peritoneal metastases could effectively predict OS of patients with CRCPM. Peritoneal metastasis of colorectal cancer decreased the infiltration level of T and B cells.
免疫评分可以准确预测 I-III 期结直肠癌患者的预后。然而,它是否可用于预测结直肠癌腹膜转移(CRCPM)的预后仍有待验证。我们分析了 68 例 CRCPM 患者的腹膜和卵巢转移情况。免疫评分(IS)基于 CD3+和 CD8+T 细胞的浸润水平,而 TBM 评分则源自 CD3+、CD8+、CD20+和 CD163+细胞浸润水平到肿瘤微环境(TME)。采用 Kaplan-Meier 曲线和 Cox 多因素模型分析 IS 和 TBM 评分对 CRCPM 患者无复发生存(RFS)和总生存(OS)的预测价值。采用 t 检验比较原发灶、腹膜转移和卵巢转移中不同免疫细胞亚群浸润水平的差异。CRCPM 患者 IS(>1)、TBM1 评分(≥2)或 TBM2 评分(≥2)较高者 OS 显著延长(IS:中位 OS,未达到 vs 23 个月,=0.0078;TBM1:未达到 vs 21.5 个月,=0.013;TBM2:39.3 个月 vs 15.2 个月,=0.001)。另一方面,IS 较高的患者 RFS 有改善趋势(13.4 个月 vs 11.0 个月,=0.067)。然而,TBM1 和 TBM2 评分对 RFS 无预测价值。多因素分析显示,IS、TBM1 和 TBM2 可准确预测 OS,但不能预测 RFS。最后,与原发灶组织相比,腹膜转移组织和卵巢转移组织中 CD3+T 细胞、CD8+T 细胞、CD20+B 细胞和 CD68+巨噬细胞的浸润水平显著升高。腹膜转移的结直肠癌降低了 T 细胞和 B 细胞的浸润水平。IS 和 TBM 评分可有效预测 CRCPM 患者的 OS。