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. 2014 Jan 1;3(1):e27403.
doi: 10.4161/onci.27403.

Tumor-infiltrating lymphocytes favor the response to chemoradiotherapy of head and neck cancer

Affiliations

Tumor-infiltrating lymphocytes favor the response to chemoradiotherapy of head and neck cancer

Panagiotis Balermpas et al. Oncoimmunology. .

Abstract

Tumor-infiltrating lymphocytes (TILs) play an important role in the response of neoplastic lesions to therapy. We have recently shown that a robust tumor infiltration by CD3+ and CD8+ T cells correlates with improved disease outcome upon definitive chemoradiotherapy in patients with head and neck cancer, in a manner that is influenced by tumor compartment and human papilloma virus status. Our data highlight the prognostic and therapeutic relevance of TILs in head and neck cancer.

Keywords: HPV; head and neck cancer; prognostic value; radiotherapy; tumor infiltrating lymphocytes.

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Figures

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Figure 1. Tumor-infiltrating lymphocytes favor the response to chemoradiotherapy of head and neck cancer. Patients with head and neck squamous cell carcinoma (HNSCC) manifesting a robust tumor infiltration by CD8+ T cells before therapy (baseline) had a favorable clinical outcome, whereas patients with reduced amount of CD8+ (and CD3+) tumor-infiltrating lymphocytes presented worse prognosis upon chemoradiotherapy (CRT). Interestingly, high levels of CD8+ TILs were associated with excellent clinical outcome in human papillomavirus (HPV) patients, whereas a only moderate benefit was observed in HPV16+ individuals. In contrast, patients with limited CD8+ T-cell infiltration had an unfavorable prognosis, irrespective of their HPV status. Of note, our cohort included patients with HNSCC from various anatomical locations and not only the oropharynx, which is the common site of HPV-associated HNSCCs. Based on the levels of CD8+ T-cell infiltration at baseline, novel immunotherapeutic strategies could be explored in combination with CRT to improve disease outcome in HNSCC patients.

References

    1. Argiris A, Karamouzis MV, Raben D, Ferris RL. Head and neck cancer. Lancet. 2008;371:1695–709. doi: 10.1016/S0140-6736(08)60728-X. - DOI - PMC - PubMed
    1. Lesterhuis WJ, Haanen JB, Punt CJ. Cancer immunotherapy--revisited. Nat Rev Drug Discov. 2011;10:591–600. doi: 10.1038/nrd3500. - DOI - PubMed
    1. Bhardwaj N. Harnessing the immune system to treat cancer. J Clin Invest. 2007;117:1130–6. doi: 10.1172/JCI32136. - DOI - PMC - PubMed
    1. Balermpas P, Michel Y, Wangenblast J, Seitz O, Weiss C, Rödel F, Rödel C, Fokas E. Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer. Br J Cancer. 2013 doi: 10.1038/bjc.2013.640. Forthcoming. - DOI - PMC - PubMed
    1. Gooden MJ, de Bock GH, Leffers N, Daemen T, Nijman HW. The prognostic influence of tumour-infiltrating lymphocytes in cancer: a systematic review with meta-analysis. Br J Cancer. 2011;105:93–103. doi: 10.1038/bjc.2011.189. - DOI - PMC - PubMed

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