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Poster Presentation
Prognosis of tumor infiltrating lymphocytes in operable tongue cancer patients
  1. Wan-Yu Chen1,
  2. Yih-Leong Chang2,
  3. Sung-Hsin Kuo1 and
  4. Ann-Lii Cheng3
  1. Aff1 grid.412094.a0000000405727815Division of Radiation Oncology, Department of OncologyNational Taiwan University Hospital Taipei Taiwan
  2. Aff2 grid.19188.390000000405460241Department of PathologyNational Taiwan University Hospital and National Taiwan University College of Medicine Taipei Taiwan
  3. Aff3 grid.412094.a0000000405727815Department of OncologyNational Taiwan University Hospital Taipei Taiwan

https://doi.org/10.1186/2051-1426-2-S3-P198

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    Meeting abstracts

    Background

    The immune microenvironment is important to the pathophysiology of head and neck squamous cell carcinoma (HNSCC). Our aim was to investigate the prognostic significance of tumour-infiltrating lymphocytes (TILs) in operable tongue cancer patients treated with curative surgery and adjuvant radiotherapy with or without chemotherapy.

    Patients and methods

    The presence of CD3+, CD4+, CD8+ and FOXP3+ TILs in tumor tissues obtained from 93 patients during surgery were examined by immunohistochemistry. Correlation between clinicopathological features and TILs was investigated. The prognostic roles of TILs for local recurrence-free survival (LRFS), regional recurrence-free survival (RRFS), distant metastasis-free survival (DMFS) and overall survival (OS) were analyzed.

    Results

    Median follow up time was 31.4 months (range, 0.2-99.8 months). Higher number of CD4+ cells (p = 0.006), higher CD4/FOXP3 ratio (p = 0.012), lower CD3/CD4 ratio (p = 0.043), and higher CD4/CD8 ratio (p = 0.006) were correlated with the absence of lymphovascularinvasion (LVI). Patients with lower FOXP3+ TILs and higher CD8/FOXP3 ratio had marginally better RRFS (p = 0.071, and p = 0.069, respectively) (Figure 1 and Figure 2.). Patients with higher CD4/CD3 ratio had a significantly better DMFS (p = 0.036) (Figure 3).

    Figure 1
    Figure 1

    Regional recurrence-free survival (RRFS) according to FOXP3+ TILs.

    Figure 2
    Figure 2

    RRFS according to CD8/FOXP3 ratio.

    Figure 3
    Figure 3

    Distant metastasis-free survival (DMFS) according to CD4/CD3 ratio.

    Conclusion

    CD4+ TILs and its ratio to other TILs were inversely correlated with LVI. Higher CD4/CD3 ratio predicts better DMFS. Prognostic role of FOXP3 in RRFS was marginally significant and warrants further investigation.