» Articles » PMID: 39272905

Advancements in TGF-β Targeting Therapies for Head and Neck Squamous Cell Carcinoma

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2024 Sep 14
PMID 39272905
Authors
Affiliations
Soon will be listed here.
Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth leading cause of cancer worldwide according to GLOBOCAN estimates from 2022. Current therapy options for recurrent or metastatic disease are limited to conventional cytotoxic chemotherapy and immunotherapy, with few targeted therapy options readily available. Recent single-cell transcriptomic analyses identified TGF-β signaling as an important mediator of functional interplays between cancer-associated fibroblasts and a subset of mesenchymal cancer cells. This signaling was shown to drive invasiveness, treatment resistance, and immune evasion. These data provide renewed interest in the TGF-β pathway as an alternative therapeutic target, prompting a critical review of previous clinical data which suggest a lack of benefit from TGF-β inhibitors. While preclinical data have demonstrated the great anti-tumorigenic potential of TGF-β inhibitors, the underwhelming results of ongoing and completed clinical trials highlight the difficulty actualizing these benefits into clinical practice. This topical review will discuss the relevant preclinical and clinical findings for TGF-β inhibitors in HNSCC and will explore the potential role of patient stratification in the development of this therapeutic strategy.

References
1.
Chow L, Haddad R, Gupta S, Mahipal A, Mehra R, Tahara M . Antitumor Activity of Pembrolizumab in Biomarker-Unselected Patients With Recurrent and/or Metastatic Head and Neck Squamous Cell Carcinoma: Results From the Phase Ib KEYNOTE-012 Expansion Cohort. J Clin Oncol. 2016; 34(32):3838-3845. PMC: 6804896. DOI: 10.1200/JCO.2016.68.1478. View

2.
Yu C, Liu Y, Huang D, Dai Y, Cai G, Sun J . TGF-β1 mediates epithelial to mesenchymal transition via the TGF-β/Smad pathway in squamous cell carcinoma of the head and neck. Oncol Rep. 2011; 25(6):1581-7. DOI: 10.3892/or.2011.1251. View

3.
Robbins Y, Friedman J, Redman J, Sievers C, Lassoued W, Gulley J . Tumor cell HLA class I expression and pathologic response following neoadjuvant immunotherapy for newly diagnosed head and neck cancer. Oral Oncol. 2023; 138:106309. PMC: 9974754. DOI: 10.1016/j.oraloncology.2023.106309. View

4.
Zhang J, Yi J, Zhou P . Development of bispecific antibodies in China: overview and prospects. Antib Ther. 2021; 3(2):126-145. PMC: 7990247. DOI: 10.1093/abt/tbaa011. View

5.
Boreddy S, Nair R, Pandey P, Kuriakose A, Marigowda S, Dey C . BCA101 Is a Tumor-Targeted Bifunctional Fusion Antibody That Simultaneously Inhibits EGFR and TGFβ Signaling to Durably Suppress Tumor Growth. Cancer Res. 2023; 83(11):1883-1904. PMC: 10236157. DOI: 10.1158/0008-5472.CAN-21-4425. View