Programmed Death-Ligand 1 Expression in Non-Small Cell Lung Carcinoma Biopsies and Its Association with Tumor Infi

Abstract

Insights

Programmed death-ligand 1 (PD-L1) expression in non-small cell lung carcinoma (NSCLC) correlates with tumor-infiltrating lymphocytes (TIL). Desmoplastic tumors show lower PD-L1 and TIL, suggesting immunotherapy combined with TGF-β blockade may benefit these patients.

Area of Science:

  • Oncology
  • Immunology
  • Pathology

Background:

  • Immunotherapy targeting the PD-1/PD-L1 pathway is a primary treatment for non-small cell lung carcinoma (NSCLC).
  • Programmed death-ligand 1 (PD-L1) expression is the sole validated predictive biomarker for immunotherapy in NSCLC, despite limitations.
  • Tumor-infiltrating lymphocytes (TIL) within the tumor microenvironment have demonstrated predictive value for immunotherapy response.

Purpose of the Study:

  • To retrospectively analyze 134 NSCLC resection specimens.
  • To investigate the association between PD-L1 expression, TIL presence, and tumor desmoplasia.
  • To evaluate PD-L1 expression on tumor cells and TILs in relation to tumor characteristics.

Main Methods:

  • Immunohistochemistry was used to assess PD-L1 expression on tumor cells and TILs (using anti-PD-L1 clone 22C3 and anti-CD3 antibody).
  • PD-L1 was quantified using the tumor proportion score (TPS) (<1%, 1-49%, 50%).
  • TILs were evaluated using the percentage of stromal TIL (PST) system (<10%, 10-49%, 50%), with statistical analysis via the Cochran-Armitage test.

Main Results:

  • Higher PD-L1 expression was observed in tumors with PST 10-49% and 50% compared to PST <10% across adenocarcinoma and squamous cell carcinoma subtypes (p=0.008-0.028).
  • PD-L1 expression in TILs correlated with PST in squamous cell carcinomas (p=0.025) but not in adenocarcinomas.
  • Desmoplastic tumors exhibited significantly lower TPS and PST values.

Conclusions:

  • PD-L1 expression in NSCLC is linked to the presence of TILs.
  • Desmoplastic tumor areas represent immunologically less active microenvironments.
  • Combination therapy with anti-PD-1/PD-L1 agents and TGF-β pathway inhibitors shows promise for desmoplastic NSCLC.