The Use of Immune Regulation in Treating Head and Neck Squamous Cell Carcinoma (HNSCC)

被引:18
作者
Wang, Che-Wei [1 ,2 ]
Biswas, Pulak Kumar [3 ]
Islam, Atikul [1 ]
Chen, Mu-Kuan [2 ]
Chueh, Pin Ju [1 ]
机构
[1] Natl Chung Hsing Univ, Inst Biomed Sci, Taichung 40227, Taiwan
[2] Changhua Christian Hosp, Dept Otorhinolaryngol Head & Neck Surg, Changhua 50006, Taiwan
[3] Natl Cheng Kung Univ, Inst Mol Med, Tainan 70101, Taiwan
关键词
immunotherapy; immune checkpoint inhibitors; head and neck squamous cell carcinoma (HNSCC); oral carcinoma; programmed cell death protein 1; programmed death ligand-1 (PD-1/PD-L1); cytotoxic T-lymphocyte-associated protein 4 (CTLA-4); tumor microenvironment; combination therapy; T-CELLS; PD-L1; EXPRESSION; OPEN-LABEL; CANCER; THERAPY; TUMOR; ACTIVATION; RECURRENT; RECEPTOR; IMMUNOTHERAPY;
D O I
10.3390/cells13050413
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunotherapy has emerged as a promising new treatment modality for head and neck cancer, offering the potential for targeted and effective cancer management. Squamous cell carcinomas pose significant challenges due to their aggressive nature and limited treatment options. Conventional therapies such as surgery, radiation, and chemotherapy often have limited success rates and can have significant side effects. Immunotherapy harnesses the power of the immune system to recognize and eliminate cancer cells, and thus represents a novel approach with the potential to improve patient outcomes. In the management of head and neck squamous cell carcinoma (HNSCC), important contributions are made by immunotherapies, including adaptive cell therapy (ACT) and immune checkpoint inhibitor therapy. In this review, we are focusing on the latter. Immune checkpoint inhibitors target proteins such as programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) to enhance the immune response against cancer cells. The CTLA-4 inhibitors, such as ipilimumab and tremelimumab, have been approved for early-stage clinical trials and have shown promising outcomes in terms of tumor regression and durable responses in patients with advanced HNSCC. Thus, immune checkpoint inhibitor therapy holds promise in overcoming the limitations of conventional therapies. However, further research is needed to optimize treatment regimens, identify predictive biomarkers, and overcome potential resistance mechanisms. With ongoing advancements in immunotherapy, the future holds great potential for transforming the landscape of oral tumor treatment and providing new hope for patients.
引用
收藏
页数:22
相关论文
共 140 条
[1]  
Agne G., 2022, Arch Head Neck Surg, V51, DOI [10.4322/ahns.2022.0013, DOI 10.4322/AHNS.2022.0013]
[2]   Tumor microenvironment and Oral Squamous Cell Carcinoma: A crosstalk between the inflammatory state and tumor cell migration [J].
Alves, Alessandro ;
Diel, Leonardo ;
Ramos, Grasieli ;
Pinto, Antonio ;
Bernardi, Lisiane ;
Yates, John, III ;
Lamers, Marcelo .
ORAL ONCOLOGY, 2021, 112
[3]   Promotion of tissue inflammation by the immune receptor Tim-3 expressed on innate immune cells [J].
Anderson, Ana C. ;
Anderson, David E. ;
Bregoli, Lisa ;
Hastings, William D. ;
Kassam, Nasim ;
Lei, Charles ;
Chandwaskar, Rucha ;
Karman, Jozsef ;
Su, Ee W. ;
Hirashima, Mitsuomi ;
Bruce, Jeffrey N. ;
Kane, Lawrence P. ;
Kuchroo, Vijay K. ;
Hafler, David A. .
SCIENCE, 2007, 318 (5853) :1141-1143
[4]   Hyperprogressive Disease: Main Features and Key Controversies [J].
Arasanz, Hugo ;
Zuazo, Miren ;
Bocanegra, Ana ;
Chocarro, Luisa ;
Blanco, Ester ;
Martinez, Maite ;
Morilla, Idoia ;
Fernandez, Gonzalo ;
Teijeira, Lucia ;
Morente, Pilar ;
Echaide, Miriam ;
Castro, Natalia ;
Fernandez, Leticia ;
Garnica, Maider ;
Ramos, Pablo ;
Escors, David ;
Kochan, Grazyna ;
Vera, Ruth .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (07)
[5]   IFN-γ-related mRNA profile predicts clinical response to PD-1 blockade [J].
Ayers, Mark ;
Lunceford, Jared ;
Nebozhyn, Michael ;
Murphy, Erin ;
Loboda, Andrey ;
Kaufman, David R. ;
Albright, Andrew ;
Cheng, Jonathan D. ;
Kang, S. Peter ;
Shankaran, Veena ;
Piha-Paul, Sarina A. ;
Yearley, Jennifer ;
Seiwert, Tanguy Y. ;
Ribas, Antoni ;
McClanahan, Terrill K. .
JOURNAL OF CLINICAL INVESTIGATION, 2017, 127 (08) :2930-2940
[6]   Prognostic Significance of CD4+and CD8+Tumor-Infiltrating Lymphocytes in Head and Neck Squamous Cell Carcinoma: A Meta-Analysis [J].
Borsetto, Daniele ;
Tomasoni, Michele ;
Payne, Karl ;
Polesel, Jerry ;
Deganello, Alberto ;
Bossi, Paolo ;
Tysome, James R. ;
Masterson, Liam ;
Tirelli, Giancarlo ;
Tofanelli, Margherita ;
Boscolo-Rizzo, Paolo .
CANCERS, 2021, 13 (04) :1-15
[7]   The Role of Soluble LAG3 and Soluble Immune Checkpoints Profile in Advanced Head and Neck Cancer: A Pilot Study [J].
Botticelli, Andrea ;
Zizzari, Ilaria Grazia ;
Scagnoli, Simone ;
Pomati, Giulia ;
Strigari, Lidia ;
Cirillo, Alessio ;
Cerbelli, Bruna ;
Di Filippo, Alessandra ;
Napoletano, Chiara ;
Scirocchi, Fabio ;
Rughetti, Aurelia ;
Nuti, Marianna ;
Mezi, Silvia ;
Marchetti, Paolo .
JOURNAL OF PERSONALIZED MEDICINE, 2021, 11 (07)
[8]   Pembrolizumab alone or with chemotherapy versus cetuximab with chemotherapy for recurrent or metastatic squamous cell carcinoma of the head and neck (KEYNOTE-048): a randomised, open-label, phase 3 study [J].
Burtness, Barbara ;
Harrington, Kevin J. ;
Greil, Richard ;
Soulieres, Denis ;
Tahara, Makoto ;
de Castro, Gilberto, Jr. ;
Psyrri, Amanda ;
Baste, Neus ;
Neupane, Prakash ;
Bratland, Ase ;
Fuereder, Thorsten ;
Hughes, Brett G. M. ;
Mesia, Ricard ;
Ngamphaiboon, Nuttapong ;
Rordorf, Tamara ;
Ishak, Wan Zamaniah Wan ;
Hong, Ruey-Long ;
Mendoza, Rene Gonzalez ;
Roy, Ananya ;
Zhang, Yayan ;
Gumuscu, Burak ;
Cheng, Jonathan D. ;
Jin, Fan ;
Rischin, Danny .
LANCET, 2019, 394 (10212) :1915-1928
[9]   Hypoxia and the Metastatic Niche [J].
Chan, Cerise Yuen-Ki ;
Yuen, Vincent Wai-Hin ;
Wong, Carmen Chak-Lui .
HYPOXIA AND CANCER METASTASIS, 2019, 1136 :97-112
[10]   Molecular Pathways: Next-Generation Immunotherapy-Inhibiting Programmed Death-Ligand 1 and Programmed Death-1 [J].
Chen, Daniel S. ;
Irving, Bryan A. ;
Hodi, F. Stephen .
CLINICAL CANCER RESEARCH, 2012, 18 (24) :6580-6587