Department of Clinical Oral Oncology, Graduate School of Biomedical Sciences, Nagasaki University, 1-7-1 Sakamoto, Nagasaki, 852-8588, Japan.
Department of Dentistry and Oral Surgery, Shinshu University School of Medicine, Matsumoto, Nagano, 390-8621, Japan.
Pathol Oncol Res. 2020 Apr;26(2):735-742. doi: 10.1007/s12253-019-00606-3. Epub 2019 Feb 14.
While neoadjuvant chemotherapy (NAC) for patients with oral tongue squamous cell carcinoma (OTSCC) may improve tumor microenvironment, it may lead to local immune suppression caused by residual cancer cells. The efficacy of NAC is therefore controversial. In our study, we investigated tumor microenvironments after NAC using immune checkpoint molecules, and evaluated the association between tumor microenvironments, clinicopathological factors and outcomes. We reviewed the records of 121 patients who underwent radical surgery for OTSCC between April 2001 and March 2015. Patients with a positive surgical margin and a follow up period of less than 6 months were excluded. For these patients, programmed death 1 (PD-1) and programmed death ligand 1 (PD-L1) expressions were immunohistochemically examined. The expression of PD-1 and PD-L1 were significantly associated with local recurrence in patients with OTSCC (P < 0.01 and P < 0.01, respectively). We found a significant decrease in 5-year disease specific survival rate for patients with combined PD-1+/PD-L1+ expressions (P < 0.05). In the subgroup analysis of local recurrence between the NAC treated group and those who received surgery alone, high levels of PD-1 and PD-L1 expressions were significantly found in the former, but not in the latter group. Local recurrence in the NAC-treated group may contribute to local immune suppression in OTSCC. NAC lead to local immune suppression and immune checkpoint molecules play an important role in local recurrence in patients with OTSCC who received NAC. NAC modality can't be recommended for patients with OTSCC at present.
新辅助化疗(NAC)可改善口腔舌鳞状细胞癌(OTSCC)患者的肿瘤微环境,但可能导致残留癌细胞引起的局部免疫抑制。因此,NAC 的疗效存在争议。在我们的研究中,我们使用免疫检查点分子研究了 NAC 后的肿瘤微环境,并评估了肿瘤微环境、临床病理因素与结局之间的关系。我们回顾了 2001 年 4 月至 2015 年 3 月期间 121 例行根治性手术治疗的 OTSCC 患者的记录。排除了切缘阳性和随访时间少于 6 个月的患者。对这些患者,采用免疫组化方法检测程序性死亡受体 1(PD-1)和程序性死亡配体 1(PD-L1)的表达。PD-1 和 PD-L1 的表达与 OTSCC 患者的局部复发显著相关(P<0.01 和 P<0.01)。我们发现 PD-1+/PD-L1+ 表达的患者 5 年疾病特异性生存率显著降低(P<0.05)。在 NAC 治疗组与单纯手术组局部复发的亚组分析中,前者中 PD-1 和 PD-L1 的表达水平较高,而后者中则没有。NAC 治疗组的局部复发可能导致 OTSCC 局部免疫抑制。NAC 导致局部免疫抑制,免疫检查点分子在接受 NAC 的 OTSCC 患者的局部复发中起重要作用。目前不能推荐 NAC 治疗 OTSCC 患者。