Department of Radiology, Sapporo Medical University School of Medicine, S1W16, Chuo-Ku, Sapporo, Hokkaido, 060-8543, Japan.
Department of Oral Surgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Med Mol Morphol. 2023 Dec;56(4):288-296. doi: 10.1007/s00795-023-00367-8. Epub 2023 Jul 29.
Preoperative intra-arterial chemoradiotherapy (IACRT) can improve the outcome and reduce the extent of surgery in patients with advanced oral cancer. However, the response to this regimen varies among patients, which may be related to the immune status of the tumor. We investigated the effects of proteins involved in tumor immunity on the outcomes of combined IACRT and surgery for oral cancer. We examined CD8 + and FoxP3 + tumor-infiltrating lymphocytes (TILs) and programmed death ligand 1 (PD-L1) expression on immune cells and tumor cells in pretreatment biopsy samples from 69 patients diagnosed with oral cancer treated with IACRT at our institution during 2000-2020. Patients with abundant CD8 + TILs had significantly better 5-year disease-specific survival (DSS) compared to that of patients with less infiltration of these cells (P = 0.016). Patients with higher FoxP3 + T-cells invasion had significantly better DSS compared to that of less FoxP3 (P = 0.005). Patients with high PD-L1 expression in tumor cells and immune cells had significantly better DSS than that of patients with low PD-L1 expression in these cells (P = 0.009 and P = 0.025, respectively). Collectively, these results suggest that the tumor immune microenvironment could affect outcomes of IACRT treatment in oral cancer.
术前动脉内化疗放疗(IACRT)可改善晚期口腔癌患者的预后并减少手术范围。然而,这种治疗方案在不同患者中的反应存在差异,这可能与肿瘤的免疫状态有关。我们研究了肿瘤免疫相关蛋白对接受 IACRT 联合手术治疗的口腔癌患者结局的影响。我们检测了 69 例于 2000 年至 2020 年在我院接受 IACRT 治疗的口腔癌患者的预处理活检样本中免疫细胞和肿瘤细胞上的 CD8 ⁇ 和 FoxP3 ⁇ 肿瘤浸润淋巴细胞(TIL)和程序性死亡配体 1(PD-L1)的表达。与 CD8 ⁇ TIL 浸润较少的患者相比,CD8 ⁇ TIL 浸润丰富的患者具有显著更好的 5 年疾病特异性生存率(DSS)(P ⁇ 0.016)。FoxP3 ⁇ T 细胞浸润较高的患者与 FoxP3 ⁇ 较少的患者相比,具有显著更好的 DSS(P ⁇ 0.005)。肿瘤细胞和免疫细胞中 PD-L1 高表达的患者与这些细胞中 PD-L1 低表达的患者相比,具有显著更好的 DSS(P ⁇ 0.009 和 P ⁇ 0.025)。总之,这些结果表明肿瘤免疫微环境可能影响口腔癌 IACRT 治疗的结局。