ORIGINAL ARTICLE
The prognostic significance of tumour infiltrating lymphocytes in oral squamous cell carcinoma
 
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1
Department of Pathology, MedLifeCover, Krosno, Poland
 
2
Department of Oral and Maxillofacial Surgery, Clinical Voivodeship Hospital Nr 1, Rzeszow, Poland
 
3
Department of Emergency Medical Service, Faculty of Medicine, the University of Rzeszow, Poland
 
4
Intensive Care Unit and Anaesthesia with Acute Poisons Centre, Clinical Voivodeship Hospital Nr 2, Rzeszow, Poland
 
5
retired from Department of Pathology, Clinical Voivodeship Hospital Nr 1, Rzeszow, Poland
 
6
Department of Tumour Pathology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, Krakow Branch, Krakow, Poland
 
 
Publication date: 2020-03-06
 
 
Pol J Pathol 2019;70(4):277-285
 
KEYWORDS
ABSTRACT
Currently there is being conducted an extensive search to find new prognostic factors in oral squamous cell carcinoma which would assist in better patient management. One of the most promising prognostic markers is the density of tumour infiltrating lymphocytes. 100 cases of patients with oral squamous cell carcinoma that underwent surgical resection between 2006 and June 2016 at our institution were included in this study. From each case the most representative HE stained slide was identified and the density of tumour infiltrating lymphocytes were classified as non-brisk or brisk, which was included in the survival analysis. Upon analysis there was a strong correlation between non-brisk (n = 28) and brisk (n = 72) tumour infiltrating lymphocytes and the primary clinical outcomes: overall survival (p = 0.0472) and local recurrence-free survival (p = 0.00037). Univariate and multivariate Cox regression model confirmed the high prognostic value of tumour infiltrating lymphocytes as the independent prognostic indicator of better survival, being even superior, in our study, to the traditional pTNM system. This study provides robust evidence that the density of tumour infiltrating lymphocytes demonstrates a high prognostic significance in oral squamous cell carcinoma.
REFERENCES (32)
1.
IARC W. Estimated number of new cases in 2018, worldwide, both sexes, all ages [Internet]. International Agency for Research on Cancer. 2018 [cited 2019 Apr 22]. Available from: http://gco.iarc.fr/today/onlin....
 
2.
Dikshit R, Gupta PC, Ramasundarahettige C, et al. Cancer mortality in India: A nationally representative survey. Lancet 2012; 379: 1807-1816.
 
3.
Zygogianni AG, Kyrgias G, Karakitsos P, et al. Oral squamous cell cancer: Early detection and the role of alcohol and smoking. Head Neck Oncol 2011; 3: 2; doi: 10.1186/1758-3284-3-2.
 
4.
Brierley JD, Gospodarowicz MK, Wittekind C. TNM classification of malignant tumours – 8th edition. Union Int Cancer Control 2016.
 
5.
Helliwell T, Woolgar J. Dataset for histopathology reporting of mucosal malignancies of the oral cavity [Internet]. The Royal College of Pathologists. 2013 [cited 2019 Apr 22]. Available from: https://www.rcpath.org/profess....
 
6.
Seethala RR, Bullock MJ, Carlson DL, et al. Protocol for the Examination of Specimens from Patients with Cancers of the Lip and Oral Cavity [Internet]. College of American Pathologists. 2017 [cited 2019 Apr 22]. Available from: http://www.cap.org/ShowPropert... Folders/WebContent/pdf/cp-lip-oralcavity-17protocol-4000.pdf.
 
7.
El-Naggar AK, Chan JK, Grandis JR, et al. WHO Classification of Head and Neck Tumours. Fourth edition. WHO classification of tumours of the oral cavity and mobile tounge. IARC, Lyon 2017.
 
8.
Bloebaum M, Poort L, Böckmann R, et al. Survival after curative surgical treatment for primary oral squamous cell carcinoma. J Craniomaxillofac Surg 2014; 42: 1572-1576.
 
9.
Clark WH, From L, Bernardino EA, et al. The histogenesis and biologic behavior of primary human malignant melanomas of the skin. Cancer Res 1969; 29: 705-727.
 
10.
Clemente CG, Mihm MC, Bufalino R, et al. Prognostic value of tumor infiltrating lymphocytes in the vertical growth phase of primary cutaneous melanoma. Cancer 1996; 77: 1303-1310.
 
11.
Clark WH, Elder DE, Guerry D, et al. Model predicting survival in stage I melanoma based on tumor progression. J Natl Cancer Inst 1989; 81: 1893-1904.
 
12.
Salgado R, Denkert C, Demaria S, et al. The evaluation of tumor-infiltrating lymphocytes (TILS) in breast cancer: Recommendations by an International TILS Working Group 2014. Ann Oncol 2015; 26: 259-271.
 
13.
Remark R, Becker C, Gomez JE, et al. The non-small cell lung cancer immune contexture: A major determinant of tumor characteristics and patient outcome. Am J Respir Crit Care Med 2015; 191: 377-390.
 
14.
Zhang L, Conejo-Garcia JR, Katsaros D, et al. Intratumoral T cells, recurrence, and survival in epithelial ovarian cancer. N Engl J Med 2003; 348: 203-213.
 
15.
Wada Y, Nakashima O, Kutami R, et al. Clinicopathological study on hepatocellular carcinoma with lymphocytic infiltration. Hepatology 1998; 27: 407-414.
 
16.
Teng F, Mu D, Meng X, et al. Tumor infiltrating lymphocytes (TILs) before and after neoadjuvant chemoradiotherapy and its clinical utility for rectal cancer. Am J Cancer Res 2015; 5: 2064-2074.
 
17.
Horn T, Laus J, Seitz AK, et al. The prognostic effect of tumour-infiltrating lymphocytic subpopulations in bladder cancer. World J Urol 2016; 34: 181-187.
 
18.
Uppaluri R, Dunn GP, Lewis JS. Focus on TILs: Prognostic significance of tumor infiltrating lymphocytes in head and neck cancers. Cancer Immunity 2008; 8: 16.
 
19.
Vassilakopoulou M, Avgeris M, Velcheti V, et al. Evaluation of PD-L1 expression and associated tumor-infiltrating lymphocytes in laryngeal squamous cell carcinoma. Clin Cancer Res 2016; 22: 704-713.
 
20.
Stasikowska-Kanicka O, W¹growska-Danilewicz M, Danilewicz M. Immunohistochemical analysis of Foxp3+, CD4+, CD8+ cell infiltrates and PD-L1 in oral squamous cell carcinoma. Pathol Oncol Res 2018; 24: 497-505.
 
21.
Sanoǧlu T, Yilmaz T, Gürsel B, et al. The effect of lymphocytic infiltration on clinical survival in cancer of the tongue. Eur Arch Otorhinolaryngol 1994; 251: 366-369.
 
22.
Brandwein-Gensler M, Teixeira MS, Lewis CM, et al. Oral squamous cell carcinoma: Histologic risk assessment, but not margin status, is strongly predictive of local disease-free and overall survival. Am J Surg Pathol 2005; 29: 167-178.
 
23.
Chatzistamou I, Rodriguez J, Jouffroy T, et al. Prognostic significance of tumor shape and stromal chronic inflammatory infiltration in squamous cell carcinomas of the oral tongue. J Oral Pathol Med 2010; 39: 667-671.
 
24.
Xu Q, Wang C, Yuan X, et al. Prognostic value of tumor-infiltrating lymphocytes for patients with head and neck squamous cell carcinoma. Transl Oncol 2017; 10: 10-16.
 
25.
Hendry S, Salgado R, Gevaert T, et al. Assessing Tumor-infiltrating Lymphocytes in Solid Tumors: A Practical Review for Pathologists and Proposal for a Standardized Method from the International Immunooncology Biomarkers Working Group: Part 1: Assessing the Host Immune Response, TILs in Invasi. Adv Anat Pathol 2017; 24: 235-251.
 
26.
Dieci MV, Radosevic-Robin N, Fineberg S, et al. Update on tumor-infiltrating lymphocytes (TILs) in breast cancer, including recommendations to assess TILs in residual disease after neoadjuvant therapy and in carcinoma in situ: A report of the International Immuno-Oncology Biomarker Working Group on Bre. Semin Cancer Biol 2018; 52: 16-25.
 
27.
Russo L, Maltese A, Betancourt L, et al. Locally advanced breast cancer: Tumor-infiltrating lymphocytes as a predictive factor of response to neoadjuvant chemotherapy. Eur J Surg Oncol 2019; 45: 963-968.
 
28.
Quan H, Fang L, Pan H, et al. An adaptive immune response driven by mature, antigen-experienced T and B cells within the microenvironment of oral squamous cell carcinoma. Int J Cancer 2016; 138: 2952-2962.
 
29.
Stasikowska-Kanicka O, W¹growska-Danilewicz M, Danilewicz M. Association of infiltrating cells with microvessel density in oral squamous cell carcinoma. Pol J Pathol 2017; 68: 40-48.
 
30.
Fang J, Li X, Ma D, et al. Prognostic significance of tumor infiltrating immune cells in oral squamous cell carcinoma. BMC Cancer 2017; 17: 375.
 
31.
Maleki S, Schlecht NF, Keller C, et al. Lymphocytic Host Response to Oral Squamous Cell Carcinoma: An Adaptive T-Cell Response at the Tumor Interface. Head Neck Pathol 2011; 5: 117-122.
 
32.
Batool M, Mushtaq S, Loya A. Correlation of histological risk assessment/scoring system with lymph node metastasis and recurrence/progresiosion of disease in oral squamous cell carcinoma. PAFMJ 2015; 65: 582-586.
 
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