427PD - Prognostic significance of PD-L1 expression combined with CD8+ TIL density in stage III non-small cell lung cancer patients receiving concurrent ch...

Date 19 December 2015
Event ESMO Asia 2015 Congress
Session Thoracic cancers
Topics Anti-Cancer Agents & Biologic Therapy
Non-Small-Cell Lung Cancer, Locally Advanced
Translational Research
Surgery and/or Radiotherapy of Cancer
Presenter Norikazu Matsuo
Citation Annals of Oncology (2015) 26 (suppl_9): 125-147. 10.1093/annonc/mdv532
Authors N. Matsuo, T. Tokito, K. Azuma, H. Ishii, K. Yamada, T. Hoshino
  • Division Of Respirology, Neurology, And Rheumatology, Department Of Internal Medicine, Kurume University, 830-0011 - Kurume/JP

Abstract

Aim/Background

Previous studies of patients with recurrent cancer have indicated that clinical responses to immune checkpoint blockers are associated with elevated tumor levels of programmed cell death-ligand 1 (PD-L1) and increased numbers of tumor-infiltrating lymphocytes (TILs). We investigated the prognostic significance of PD-L1 expression and CD8+ TIL density in patients with locally advanced non-small cell lung cancer (NSCLC) receiving concurrent chemoradiotherapy (CCRT).

Methods

We retrospectively reviewed 74 consecutive patients with stage III NSCLC who had received CCRT. PD-L1 expression and CD8+ TIL density were evaluated by immunohistochemical analysis.

Results

PD-L1+ patients showed shorter progression-free survival (PFS) and overall survival (OS) than PD-L1- patients (10.8 versus 17.3 months; p = 0.73, 24.9 vs 36.9 months; p = 0.85; respectively). Univariate and multivariate analyses demonstrated that CD8+ TIL density was an independent and significant predictive factor for PFS and OS. Sub-analysis revealed that the PD-L1 + /CD8 low group had the shortest PFS (8.6 months, p = 0.024) and OS (13.9 months, p = 0.105), and that the PD-L1-/CD8 high group had the longest prognosis (median PFS and OS were not reached) among the four sub-groups.

Conclusions

Among stage III NSCLC patients who received CCRT, there was a trend for poor survival in those who expressed PD-L1. Our analysis indicated that a combination of PD-L1 expression and CD8+ TIL density was significantly associated with favorable survival in these patients. It is proposed that PD-L1 expression in combination with CD8+ TIL density could be a useful predictive biomarker in patients with stage III NSCLC.

Clinical trial identification

Disclosure

All authors have declared no conflicts of interest.