头颈部鳞状细胞癌的免疫疗法与表皮生长因子受体抑制剂联合疗法的现状与前景。

Xin Tian, Hongyan Zhang, Yiman Han, Baoru Gu, Zhenyong Zhang
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引用次数: 0

摘要

头颈部鳞状细胞癌(HNSCC)是一种预后较差的恶性肿瘤,由于其隐蔽的解剖位置和不典型的临床症状,大多数头颈部鳞状细胞癌患者都是在晚期才被确诊。该病明显易复发和转移。传统治疗方法包括手术、放疗、化疗和靶向治疗。虽然目前已确立了多种治疗策略,但由于大多数患者对传统疗法产生耐药性,因此预后仍然不佳。近年来,表皮生长因子受体(EGFR)抑制剂和免疫检查点抑制剂(ICIs)已被证明可为这类患者带来临床获益。基于抗表皮生长因子受体(EGFR)疗法和免疫疗法的良好疗效,以及将免疫疗法与抗表皮生长因子受体(EGFR)药物相结合的生物学原理,许多临床前试验和正在进行或已完成的临床试验都在探索如何利用它们的协同作用。本综述总结了将免疫疗法与表皮生长因子受体抑制剂联合用于 HNSCC 治疗的可行性,并分析了相关的生物标志物。它还总结了临床应用策略。我们发现,免疫疗法和表皮生长因子受体抑制剂联合疗法在治疗 HNSCC 患者方面前景广阔,而且安全性高,不良反应可接受。这篇综述可为未来 HNSCC 治疗方法的开发和治疗策略的制定提供有价值的见解,并为未来临床试验的设计提供有用的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current status and future prospects of combined immunotherapy and epidermal growth factor receptor inhibitors in head and neck squamous cell carcinoma.

Head and neck squamous cell carcinoma (HNSCC) is a malignancy with a poor prognosis, and the majority of patients with HNSCC are diagnosed at later stages owing to its hidden anatomical location and atypical clinical symptoms. It is notably prone to recurrence and metastasis. The traditional treatments include surgery, radiotherapy, chemotherapy, and targeted therapy. Although multiple treatment strategies have been established, the prognosis remains poor because most patients develop resistance to traditional treatments. In recent years, epidermal growth factor receptor (EGFR) inhibitors and immune checkpoint inhibitors (ICIs) have been shown to provide clinical benefits to these patients. Based on the promising results of both anti-EGFR therapy and immunotherapy, as well as the biological rationale for combining immunotherapy with anti-EGFR drugs, numerous preclinical and ongoing or completed clinical trials have explored the use of their synergistic effects. This review summarizes the feasibility of combining immunotherapy with EGFR inhibitors for HNSCC treatment and analyses the relevant biomarkers. It also summarizes the strategies for clinical applications. We found that immunotherapy and EGFR inhibitor combination therapy showed promise in treating patients with HNSCC and exhibited safety with acceptable adverse events. This review may provide valuable insights for the future development of treatments and formulation of therapeutic strategies for HNSCC, as well as useful information for the future design of clinical trials.

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