Department of Gastroenterology, Faculdade de Medicina, Instituto do Cancer do Estado de São Paulo, Hospital das Clinicas of the University of São Paulo, Universidade de São Paulo, São Paulo, Brazil.
Department of Gastroenterology, Faculdade de Medicina, Instituto do Cancer do Estado de São Paulo, Hospital das Clinicas of the University of São Paulo, Universidade de São Paulo, São Paulo, Brazil.
J Gastrointest Surg. 2024 Feb;28(2):151-157. doi: 10.1016/j.gassur.2023.12.002. Epub 2024 Feb 5.
Tumor-infiltrating lymphocytes (TILs) play a regulatory role in the tumor-associated immune response and are important in the prognosis and treatment response of several cancers. However, because of its heterogeneity, the prognostic value of TILs in gastric cancer (GC) is still controversial. Thus, this study aimed to investigate the association between the density of TILs and patients' outcomes in GC.
Patients with gastric adenocarcinoma who underwent curative intent gastrectomy were retrospectively investigated. The groups for analysis were determined on the basis of TIL intensity and percentage of CD3+ T-cell infiltration by immunohistochemical. Furthermore, Epstein-Barr virus (EBV), microsatellite instability (MSI), T-cell ratio of CD4 to CD8, and programmed death protein ligand 1 (PD-L1) status were evaluated.
A total of 345 patients were enrolled: 124 patients with GCs (35.9%) were classified as the low-CD3+ TIL group, and 221 patients with GCs (64.1%) were classified as the high-CD3+ TIL group. Poorly differentiated histology (P = .014), EBV-positive status (P < .001), PD-L1-positive status (P = .001), and CD4 < CD8 (P < .001) were associated with high-CD3+ GC. There was no difference regarding MSI status, the degree of tumor invasion (pT), the presence of lymph node metastasis, and pTNM stage between low- and high-CD3+ groups. In survival analysis, the high-CD3+ group had better disease-free survival and overall survival rates than had the low-CD3+ group (P = .055 and P = .041, respectively). In the multivariate analysis, total gastrectomy, lymph node metastasis, advanced pT stage, and low CD3+ levels were independent factors related to worse survival.
High CD3+ TILs levels were significantly associated with improved survival and could serve as prognostic biomarkers in GC. In addition, CD3+ T-cell infiltration was related to both EBV-positive and PD-L1-positive GC and may assist in the investigation of targets in immunotherapy.
肿瘤浸润淋巴细胞(TILs)在肿瘤相关免疫反应中发挥调节作用,对多种癌症的预后和治疗反应具有重要意义。然而,由于其异质性,TILs 在胃癌(GC)中的预后价值仍存在争议。因此,本研究旨在探讨 TILs 密度与 GC 患者结局之间的关系。
回顾性分析接受根治性胃切除术的胃腺癌患者。根据免疫组化 CD3+T 细胞浸润强度和百分比确定分析组。此外,还评估了 Epstein-Barr 病毒(EBV)、微卫星不稳定性(MSI)、CD4/CD8 T 细胞比值和程序性死亡蛋白配体 1(PD-L1)状态。
共纳入 345 例患者:124 例 GC 患者(35.9%)被分为低 CD3+TIL 组,221 例 GC 患者(64.1%)被分为高 CD3+TIL 组。低分化组织学(P=.014)、EBV 阳性状态(P<.001)、PD-L1 阳性状态(P=.001)和 CD4<CD8(P<.001)与高 CD3+GC 相关。低和高 CD3+组之间在 MSI 状态、肿瘤侵袭程度(pT)、淋巴结转移存在以及 pTNM 分期方面无差异。在生存分析中,高 CD3+组的无病生存率和总生存率均高于低 CD3+组(P=.055 和 P=.041)。在多因素分析中,全胃切除术、淋巴结转移、晚期 pT 分期和低 CD3+水平是与生存较差相关的独立因素。
高 CD3+TILs 水平与生存改善显著相关,可作为 GC 的预后生物标志物。此外,CD3+T 细胞浸润与 EBV 阳性和 PD-L1 阳性 GC 相关,可能有助于免疫治疗靶点的研究。