Ono Takeharu, Azuma Koichi, Kawahara Akihiko, Sasada Tetsuro, Hattori Satoshi, Sato Fumihiko, Shin Buichiro, Chitose Shun-Ich, Akiba Jun, Hirohito Umeno
Department of Otolaryngology-Head and Neck Surgery, Kurume University School of Medicine, Kurume, Japan.
Division of Respirology, Neurology, and Rheumatology, Department of Internal Medicine, Kurume University School of Medicine, Kurume, Japan.
Oncotarget. 2017 Oct 6;8(54):92699-92714. doi: 10.18632/oncotarget.21564. eCollection 2017 Nov 3.
Limited information is available regarding the immune-related prognostic factors of patients with advanced hypopharyngeal squamous cell carcinoma (HPSCC). The expression of programmed cell death-ligand 1 (PD-L1) in tumor cells contributes to a mechanism that allows cancer cells to escape immune surveillance. We investigated whether PD-L1 or human leukocyte antigen (HLA) class I expression in tumor cells and the tumor-infiltrating lymphocyte (TIL) density were associated with the tumor response to neoadjuvant chemotherapy (NAC) and survival in patients with advanced HPSCC. We retrospectively reviewed 83 consecutive patients with stage III or IV HPSCC who received NAC. We evaluated PD-L1 and HLA class I expression and TIL density using immunohistochemistry. Univariate and multivariate analyses demonstrated that CD8 TIL density was an independent and significant predictive factor for the response to NAC, progression-free survival (PFS) and overall survival (OS), whereas PD-L1 or HLA class I expression did not significantly correlate. The subgroup analysis revealed that a higher CD8 TIL density without detectable PD-L1 expression tended to be associated with longer patient survival. These results suggest that PD-L1 expression levels combined with CD8 TIL density may serve as a predictive biomarker for patients with stage III or IV HPSCC receiving NAC.
关于晚期下咽鳞状细胞癌(HPSCC)患者免疫相关预后因素的信息有限。肿瘤细胞中程序性细胞死亡配体1(PD-L1)的表达促成了癌细胞逃避免疫监视的机制。我们研究了肿瘤细胞中PD-L1或人类白细胞抗原(HLA)I类的表达以及肿瘤浸润淋巴细胞(TIL)密度是否与晚期HPSCC患者对新辅助化疗(NAC)的肿瘤反应和生存相关。我们回顾性分析了83例连续接受NAC的III期或IV期HPSCC患者。我们使用免疫组织化学评估PD-L1和HLA I类的表达以及TIL密度。单因素和多因素分析表明,CD8 TIL密度是NAC反应、无进展生存期(PFS)和总生存期(OS)的独立且显著的预测因素,而PD-L1或HLA I类表达无显著相关性。亚组分析显示,较高的CD8 TIL密度且无可检测的PD-L1表达往往与患者更长的生存期相关。这些结果表明,PD-L1表达水平与CD8 TIL密度相结合可能作为接受NAC的III期或IV期HPSCC患者的预测生物标志物。