Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer

被引:238
|
作者
Balermpas, P. [1 ]
Michel, Y. [2 ]
Wagenblast, J. [3 ]
Seitz, O. [4 ]
Weiss, C. [1 ]
Roedel, F. [1 ]
Roedel, C. [1 ]
Fokas, E. [1 ]
机构
[1] Goethe Univ Frankfurt, Dept Radiat Therapy & Oncol, D-60054 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Senckenberg Inst Pathol, D-60054 Frankfurt, Germany
[3] Goethe Univ Frankfurt, Dept Head & Neck Surg, D-60054 Frankfurt, Germany
[4] Goethe Univ Frankfurt, Dept Maxillofacial Surg, D-60054 Frankfurt, Germany
关键词
tumour-infiltrating lymphocytes; radiotherapy; head and neck cancer; prognostic value; SQUAMOUS-CELL CARCINOMA; HUMAN-PAPILLOMAVIRUS STATUS; CD8(+) T-CELLS; OROPHARYNGEAL CANCER; POSITIVE HEAD; SURVIVAL; RADIOTHERAPY; IMMUNOTHERAPY; P16(INK4A); EXPRESSION;
D O I
10.1038/bjc.2013.640
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We aimed to investigate the prognostic value of tumour-infiltrating lymphocytes' (TILs) expression in pretreatment specimens from patients with head and neck squamous cell carcinoma (HNSCC) treated with definitive chemoradiotherapy (CRT). Methods: The prevalence of CD3+, CD8+, CD4+ and FOXP3+ TILs was assessed using immunohistochemistry in tumour tissue obtained from 101 patients before CRT and was correlated with clinicopathological characteristics as well as local failure-free- (LFFS), distant metastases free-(DMFS), progression-free (PFS) and overall survival (OS). Survival curves were measured using the Kaplan-Meier method, and differences in survival between the groups were estimated using the log-rank test. Prognostic effects of TIL subset density were determined using the Cox regression analysis. Results: With a mean follow-up of 25 months (range, 2.3-63 months), OS at 2 years was 57.4% for the entire cohort. Patients with high immunohistochemical CD3 and CD8 expression had significantly increased OS (P = 0.024 and P = 0.028), PFS (P = 0.044 and P = 0.047) and DMFS (P = 0.021 and P = 0.026) but not LFFS (P = 0.90 and P = 0.104) in multivariate analysis that included predictive clinicopathologic factors, such as age, sex, T-stage, N-stage, tumour grading and localisation. Neither CD4 nor FOXP3 expression showed significance for the clinical outcome. The lower N-stage was associated with improved OS in the multivariate analysis (P = 0.049). Conclusion: The positive correlation between a high number of infiltrating CD3+ and CD8+ cells and clinical outcome indicates that TILs may have a beneficial role in HNSCC patients and may serve as a biomarker to identify patients likely to benefit from definitive CRT.
引用
收藏
页码:501 / 509
页数:9
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