Starska-Kowarska Katarzyna
Department of Physiology, Pathophysiology and Clinical Immunology, Department of Clinical Physiology, Medical University of Lodz, Żeligowskiego 7/9, 90-752 Lodz, Poland.
Department of Otorhinolaryngology, EnelMed Center Expert, Drewnowska 58, 91-001 Lodz, Poland.
Cancers (Basel). 2023 Mar 7;15(6):1642. doi: 10.3390/cancers15061642.
Head and neck squamous cell carcinoma (HNSCC) is one of the most aggressive and heterogeneous groups of human neoplasms. HNSCC is characterized by high morbidity, accounting for 3% of all cancers, and high mortality with ~1.5% of all cancer deaths. It was the most common cancer worldwide in 2020, according to the latest GLOBOCAN data, representing the seventh most prevalent human malignancy. Despite great advances in surgical techniques and the application of modern combinations and cytotoxic therapies, HNSCC remains a leading cause of death worldwide with a low overall survival rate not exceeding 40-60% of the patient population. The most common causes of death in patients are its frequent nodal metastases and local neoplastic recurrences, as well as the relatively low response to treatment and severe drug resistance. Much evidence suggests that the tumour microenvironment (TME), tumour infiltrating lymphocytes (TILs) and circulating various subpopulations of immunocompetent cells, such regulatory T cells (CD4CD25Foxp3T), cytotoxic CD3CD8 T cells (CTLs) and CD3CD4 T helper type 1/2/9/17 (Th/Th/Th/Th) lymphocytes, T follicular helper cells (T) and CD56/CD16 activated natural killer cells (NK), carcinoma-associated fibroblasts (CAFs), myeloid-derived suppressor cells (MDSCs), tumour-associated neutrophils (N1/N2 TANs), as well as tumour-associated macrophages (M1/M2 phenotype TAMs) can affect initiation, progression and spread of HNSCC and determine the response to immunotherapy. Rapid advances in the field of immuno-oncology and the constantly growing knowledge of the immunosuppressive mechanisms and effects of tumour cancer have allowed for the use of effective and personalized immunotherapy as a first-line therapeutic procedure or an essential component of a combination therapy for primary, relapsed and metastatic HNSCC. This review presents the latest reports and molecular studies regarding the anti-tumour role of selected subpopulations of immunocompetent cells in the pathogenesis of HNSCC, including HPV (HPV) and HPV (HPV) tumours. The article focuses on the crucial regulatory mechanisms of pro- and anti-tumour activity, key genetic or epigenetic changes that favour tumour immune escape, and the strategies that the tumour employs to avoid recognition by immunocompetent cells, as well as resistance mechanisms to T and NK cell-based immunotherapy in HNSCC. The present review also provides an overview of the pre- and clinical early trials (I/II phase) and phase-III clinical trials published in this arena, which highlight the unprecedented effectiveness and limitations of immunotherapy in HNSCC, and the emerging issues facing the field of HNSCC immuno-oncology.
头颈部鳞状细胞癌(HNSCC)是人类肿瘤中侵袭性最强、异质性最高的肿瘤类型之一。HNSCC的特点是发病率高,占所有癌症的3%,死亡率高,占所有癌症死亡人数的约1.5%。根据最新的全球癌症统计数据(GLOBOCAN),它是2020年全球最常见的癌症,是第七大最普遍的人类恶性肿瘤。尽管手术技术有了很大进步,现代联合化疗和细胞毒性疗法也得到了应用,但HNSCC仍然是全球主要的死亡原因之一,总体生存率较低,不超过患者群体的40%-60%。患者最常见的死亡原因是频繁的淋巴结转移和局部肿瘤复发,以及对治疗的反应相对较低和严重的耐药性。许多证据表明,肿瘤微环境(TME)、肿瘤浸润淋巴细胞(TILs)以及循环中的各种免疫活性细胞亚群,如调节性T细胞(CD4⁺CD25⁺Foxp3⁺T)、细胞毒性CD3⁺CD8⁺T细胞(CTLs)和CD3⁺CD4⁺T辅助1/2/9/17型(Th1/Th2/Th9/Th17)淋巴细胞、滤泡辅助性T细胞(Tfh)和CD56⁺/CD16⁺活化自然杀伤细胞(NK)、癌相关成纤维细胞(CAFs)、髓源性抑制细胞(MDSCs)、肿瘤相关中性粒细胞(N1/N2 TANs)以及肿瘤相关巨噬细胞(M1/M2表型TAMs),会影响HNSCC的发生、发展和扩散,并决定免疫治疗的反应。免疫肿瘤学领域的快速发展以及对肿瘤免疫抑制机制和效应的不断深入了解,使得有效的个性化免疫治疗能够作为一线治疗方法或用于原发性、复发性和转移性HNSCC联合治疗的重要组成部分。本综述介绍了有关免疫活性细胞特定亚群在HNSCC发病机制中的抗肿瘤作用的最新报道和分子研究,包括人乳头瘤病毒(HPV)阳性和HPV阴性肿瘤。文章重点关注促肿瘤和抗肿瘤活性的关键调节机制、有利于肿瘤免疫逃逸的关键基因或表观遗传变化、肿瘤用于逃避免疫活性细胞识别的策略,以及HNSCC中针对T细胞和NK细胞免疫治疗的耐药机制。本综述还概述了该领域已发表的前期和临床早期试验(I/II期)以及III期临床试验,这些试验突出了免疫治疗在HNSCC中前所未有的有效性和局限性,以及HNSCC免疫肿瘤学领域面临的新问题。