4.7 Article

PD-L1 expression correlates with tumor-infiltrating lymphocytes and better prognosis in patients with HPV-negative head and neck squamous cell carcinomas

期刊

CANCER IMMUNOLOGY IMMUNOTHERAPY
卷 69, 期 10, 页码 2089-2100

出版社

SPRINGER
DOI: 10.1007/s00262-020-02604-w

关键词

Head and neck cancer; PD-L1; Tumor-infiltrating lymphocytes; Prognosis

资金

  1. Plan Nacional de I+D+I [PI16/00280, PI19/00560, PI19/00098, CB16/12/00390, CB16/12/00443]
  2. Instituto de Investigacion Sanitaria del Principado de Asturias (ISPA)
  3. Fundacion Merck Salud [17-CC-008]
  4. Ayudas a Grupos PCTI Principado de Asturias [IDI2018/155]
  5. FEDER Funding Program from the European Union
  6. Severo Ochoa predoctoral fellowship from the Principado de Asturias [BP19-063]
  7. Spanish Ministry of Education [FPU17/01985]
  8. Servicio de Salud del Principado de Asturias, Instituto de Salud Carlos III [PT17/0015/0023]
  9. Fundacion Bancaria Cajastur and integrated in the Spanish National Biobanks Network [PT17/0015/0023]

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Introduction The importance of immune tumor microenvironment in the prognosis of patients with head and neck squamous carcinomas (HNSCC) is increasingly recognized. We analyzed the prognostic relevance of PD-L1 and PD-1 expressions in relation to the infiltration by CD8(+) and FOXP3(+) tumor-infiltrating lymphocytes (TILs). Methods Samples from 372 surgically treated HPV-negative HNSCC patients were evaluated by immunohistochemistry for PD-L1 expression [both tumor proportion score (TPS) and combined proportion score (CPS)], PD-1 expression in immune cells, and density of infiltrating CD8(+) and FOXP3(+) TILs. PD-L1 expression and CD8(+) TIL density were combined to establish the type of tumor microenvironment. Results 29.5% cases exhibited PD-L1 TPS positivity (>= 1%), whereas PD-L1 CPS positivity (>= 1%) was observed in 40% cases. 47.5% cases showed positive PD-1 expression (>= 1%). PD-L1 and PD-1 positivity correlated with a high density of both CD8(+) and FOXP3(+) TILs. In univariate analysis, PD-L1 TPS positivity (P = 0.026), PD-L1 CPS positivity (P = 0.004), high density of CD8(+) TIL (P = 0.001), and high density of FOXP3(+) TIL (P = 0.004) were associated with a better disease-specific survival (DSS). However, in multivariate analysis, only high density of CD8(+) TIL was associated with a better DSS (P = 0.002). The type of tumor microenvironment correlated with DSS (P = .008), with the better DSS observed in cases with type I (PD-L1 CPS positivity and high density of CD8(+) TIL). Conclusions High infiltration by CD8(+) TIL is associated with better survival outcomes. Positive PD-L1 expression correlates with a high infiltration by TILs, explaining its association with better prognosis.

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