The presence of tumor-infiltrating lymphocytes (TIL) is increasingly recognized as an important biomarker in head and neck squamous cell carcinoma (HNSCC). Consistent observations using a variety of techniques show that higher levels of T cells in the tumor microenvironment (TME) are associated with improved outcomes.
1-5 Since the discovery of subpopulations of TILs in the 1980s, understanding of the location, functional activity, and cell types has expanded.
6 Although TILs appear to have some prognostic value in HNSCC, their usefulness as a biomarker to determine treatment type, or impact on outcome in heterogeneous head and neck cancer subsites (oral cavity, oropharynx, larynx) has yet to be elucidated. Thus, a more accurate analysis of the potential benefit of assessing microenvironment T-cell infiltrates requires a homogenous sample of large numbers of patients with tumors of similar site with detailed information regarding other prognostic clinical characteristics, treatment regimens, and specific outcomes. Furthermore, a better understanding of TILs as a biomarker is a necessary prerequisite for improving individualized treatment that limits the intensity and morbidity of conventional treatment, and may be useful in advancing the introduction of new immunotherapy regimens.