Division of Medical Oncology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Ratchathewi, Bangkok, 10400, Thailand.
Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Med Oncol. 2019 Jan 21;36(2):21. doi: 10.1007/s12032-018-1241-1.
No predictive biomarker of immune checkpoint inhibitors in head and neck squamous cell carcinoma (HNSCC) has been well established. The impact of programmed death-ligand 1 (PD-L1) expression, CD8+ tumor-infiltrating lymphocytes (TILs), and p16 status in HNSCC is unclear and may vary according to ethnicity.
HNSCC patients treated between 2007 and 2013 were reviewed. Archival tissues were retrieved for PD-L1, CD8+ TILs, and p16 analyses. PD-L1 expression was evaluated by using the validated SP142 assay on the VENTANA platform. CD8+ TILs were defined by using semiquantitative scoring.
A total of 203 patients were analyzed. PD-L1 expression was observed in 80% of patients and was significantly associated with older age (P < 0.001). A high CD8+ TIL score (≥ 6) was significantly associated with never-smoking (P = 0.020), oral cavity cancer (P < 0.001), and stage M0 at presentation (P = 0.025). The p16 status was positive in 12% of patients. Patients with a high TIL score had a significantly longer OS (P = 0.032). Patients with PD-L1 expression of 1-49% and ≥ 50% were associated with a significantly shorter OS compared with those with PD-L1 < 1% (P = 0.027 and P = 0.011, respectively). Multivariate analysis showed that PD-L1 ≥ 50% was significantly associated with a poor OS. (HR 2.98 [95% CI 1.2-7.39]; P = 0.019.) CONCLUSIONS: A high prevalence of PD-L1 expression was observed in HNSCC using the validated SP142 assay. PD-L1 expression was associated with older age, while highly PD-L1 expression (≥ 50%) was an independent prognostic factor for poor OS in anti-PD1/PD-L1 untreated HNSCC patients.
目前尚未建立对头颈鳞状细胞癌(HNSCC)免疫检查点抑制剂的预测性生物标志物。程序性死亡配体 1(PD-L1)表达、CD8+肿瘤浸润淋巴细胞(TIL)和 HNSCC 中的 p16 状态的影响尚不清楚,并且可能因种族而异。
回顾了 2007 年至 2013 年间治疗的 HNSCC 患者。检索了存档组织以进行 PD-L1、CD8+TIL 和 p16 分析。使用 VENTANA 平台上经过验证的 SP142 测定法评估 PD-L1 表达。使用半定量评分法定义 CD8+TIL。
共分析了 203 例患者。80%的患者观察到 PD-L1 表达,与年龄较大(P <0.001)显著相关。高 CD8+TIL 评分(≥6)与从不吸烟(P = 0.020)、口腔癌(P <0.001)和初诊时 M0 期(P = 0.025)显著相关。12%的患者 p16 状态呈阳性。高 TIL 评分的患者 OS 明显更长(P = 0.032)。PD-L1 表达为 1-49%和≥50%的患者与 PD-L1 <1%的患者相比,OS 明显更短(P = 0.027 和 P = 0.011)。多变量分析显示,PD-L1≥50%与较差的 OS 显著相关。(HR 2.98 [95%CI 1.2-7.39];P = 0.019。)
使用经过验证的 SP142 测定法,在 HNSCC 中观察到 PD-L1 表达的高患病率。PD-L1 表达与年龄较大有关,而高度 PD-L1 表达(≥50%)是未经抗 PD1/PD-L1 治疗的 HNSCC 患者 OS 不良的独立预后因素。