Zolkind Paul, Uppaluri Ravindra
Department of Otolaryngology, Washington University School of Medicine, St. Louis, MO, USA.
Brigham and Women's Hospital and Dana-Farber Cancer Institute, 45 Francis Street, Boston, MA, 02215, USA.
Cancer Metastasis Rev. 2017 Sep;36(3):475-489. doi: 10.1007/s10555-017-9694-9.
Checkpoint inhibitors have recently gained FDA approval for the treatment of cisplatin-resistant recurrent and metastatic head and neck squamous cell carcinoma (HNSCC) by outperforming standard of care chemotherapy and inducing durable responses in a subset of patients. These monoclonal antibodies unleash the patient's own immune system to target cancer cells. HNSCC is a good target for these agents as there is ample evidence of active immunosurveillance in the head and neck and a number of immune evasion mechanisms by which HNSCCs form progressive disease including via the PD-1/PD-L1 axis. As HNSCCs typically possess a moderately high mutation burden, they should express numerous mutation-derived antigen targets for immune detection. However, with response rates less than 20% in clinical trials, there is a need for biomarkers to screen patients as well as clinical trials evaluating novel combinations to improve outcomes. The aim of this review is to provide historical and mechanistic context for the use of checkpoint inhibitors in head and neck cancer and provide a perspective on the role of novel checkpoints, biomarkers, and combination therapies that are evolving in the near term for patients with HNSCC.
检查点抑制剂最近已获得美国食品药品监督管理局(FDA)批准,用于治疗顺铂耐药的复发性和转移性头颈部鳞状细胞癌(HNSCC),其疗效优于标准护理化疗,并能在一部分患者中诱导持久反应。这些单克隆抗体释放患者自身的免疫系统来靶向癌细胞。HNSCC是这些药物的良好靶点,因为有充分证据表明头颈部存在活跃的免疫监视,并且HNSCC通过多种免疫逃逸机制形成进展性疾病,包括通过PD-1/PD-L1轴。由于HNSCC通常具有中等程度的高突变负担,它们应该表达大量可用于免疫检测的突变衍生抗原靶点。然而,在临床试验中,其缓解率低于20%,因此需要生物标志物来筛选患者,同时也需要进行评估新联合疗法以改善治疗结果的临床试验。本综述的目的是为头颈部癌中检查点抑制剂的使用提供历史和机制背景,并就近期正在为HNSCC患者研发的新型检查点、生物标志物和联合疗法的作用提供一个观点。