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晚期人乳头瘤病毒阴性头颈部鳞状细胞癌:未满足的需求与新兴疗法

Advanced Human Papillomavirus-Negative Head and Neck Squamous Cell Carcinoma: Unmet Need and Emerging Therapies.

作者信息

Park Robin, Chung Christine H

机构信息

Department of Head and Neck-Endocrine Oncology, Moffitt Cancer Center, Tampa, Florida.

出版信息

Mol Cancer Ther. 2024 Dec 3;23(12):1717-1730. doi: 10.1158/1535-7163.MCT-24-0281.

Abstract

Despite notable progress in the treatment of advanced head and neck squamous cell carcinoma (HNSCC), survival remains poor in patients with recurrent and/or metastatic (R/M) human papillomavirus (HPV)-negative HNSCC. Worse outcomes in patients who are HPV-negative may be partly related to loss of cell-cycle regulators and tumor suppressors as well as a noninflamed and hypoxic tumor microenvironment, both of which contribute to treatment resistance and disease progression. Anti-programmed cell death protein 1-based regimens as current standard-of-care treatment for R/M HNSCC are associated with durable responses in a limited number of patients. The anti-EGFR mAb, cetuximab, has antitumor activity in this treatment setting, but responses are short-lived and inevitably curtailed due to treatment resistance. Crosstalk between the EGFR and hepatocyte growth factor-dependent mesenchymal-epithelial transition (c-MET) receptor tyrosine kinase pathway is a known mechanism of resistance to cetuximab. Dual targeting of EGFR and c-MET pathways may overcome resistance to cetuximab in patients with HPV-negative HNSCC. Here, we review clinical data of treatments evaluated in patients with R/M HPV-negative HNSCC and highlight the potential role of combining hepatocyte growth factor/c-MET and EGFR pathway inhibitors to overcome cetuximab resistance in this population.

摘要

尽管在晚期头颈部鳞状细胞癌(HNSCC)的治疗方面取得了显著进展,但复发和/或转移性(R/M)人乳头瘤病毒(HPV)阴性的HNSCC患者的生存率仍然很低。HPV阴性患者的较差预后可能部分与细胞周期调节因子和肿瘤抑制因子的缺失以及非炎症性和低氧性肿瘤微环境有关,这两者都导致治疗抵抗和疾病进展。作为R/M HNSCC当前标准治疗方案的基于抗程序性细胞死亡蛋白1的治疗方案,仅在少数患者中产生持久反应。抗表皮生长因子受体(EGFR)单克隆抗体西妥昔单抗在这种治疗环境中具有抗肿瘤活性,但由于治疗抵抗,反应是短暂的,并且不可避免地会受到限制。EGFR与肝细胞生长因子依赖性间质-上皮转化(c-MET)受体酪氨酸激酶途径之间的串扰是对西妥昔单抗耐药的已知机制。双重靶向EGFR和c-MET途径可能克服HPV阴性HNSCC患者对西妥昔单抗的耐药性。在此,我们回顾了在R/M HPV阴性HNSCC患者中评估的治疗的临床数据,并强调了联合肝细胞生长因子/c-MET和EGFR途径抑制剂以克服该人群中西妥昔单抗耐药性的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/534d/11612620/c41e242dea7b/mct-24-0281_f1.jpg

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