HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Prognostic Impact of Programmed Death-ligand 1 and Surrounding Immune Status on Stage I Lung Cancer.

AbstractBACKGROUND:
The programmed death 1/programmed death-ligand 1 (PD-L1) pathway reportedly is as an important factor determining effects of immunotherapy; however, its prognostic impact is controversial, and its association with the surrounding immune microenvironment has not yet been elucidated.
PATIENTS AND METHODS:
We retrospectively analyzed 126 patients with pathologic stage I non-small-cell lung cancer. Patients with lepidic-dominant adenocarcinoma were excluded. PD-L1 expression was evaluated with immunohistochemistry correlated with clinicopathologic features and surrounding immune microenvironment status, including CD4, CD8, regulatory T cells, and human leukocyte antigen class I. Factors affecting prognosis were assessed by Kaplan-Meier and Cox regression analyses.
RESULTS:
Twenty-three (18.3%) patients were positive for PD-L1 expression. No significant correlation was observed between PD-L1 expression and the surrounding immune microenvironment status. The PD-L1-positive group had a worse prognosis than the PD-L1-negative group (5-year recurrence-free survival rates, 63.4% vs. 81.0%; P = .061). Among surrounding immune cells, intratumoral CD8 status had the strongest impact on prognosis (P = .12). In the intratumoral CD8-high group, PD-L1 expression demonstrated no significant prognostic impact, whereas in the intratumoral CD8-low group, patients positive for PD-L1 demonstrated a significantly worse prognosis than those negative for PD-L1 (5-year recurrence-free survival rates, 41.7% vs. 78.6%; P = .034). Multivariable Cox regression analysis revealed that 'PD-L1-positive and intratumoral CD8-low' status was an independent prognostic factor (hazard ratio, 3.80; 95% confidence interval, 1.22-10.5; P = .023).
CONCLUSIONS:
The prognostic impact of the PD-1/PD-L1 pathway may be distinct according to concurrent intratumoral CD8 status.
AuthorsYoshinori Handa, Yasuhiro Tsutani, Noriyuki Shiroma, Yuichiro Kai, Takahiro Mimae, Yoshihiro Miyata, Yukio Takeshima, Koji Arihiro, Morihito Okada
JournalClinical lung cancer (Clin Lung Cancer) Vol. 21 Issue 4 Pg. e302-e314 (07 2020) ISSN: 1938-0690 [Electronic] United States
PMID32102750 (Publication Type: Journal Article)
CopyrightCopyright © 2020 Elsevier Inc. All rights reserved.
Chemical References
  • B7-H1 Antigen
  • CD274 protein, human
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
Topics
  • Adenocarcinoma of Lung (immunology, metabolism, pathology, surgery)
  • Aged
  • B7-H1 Antigen (immunology, metabolism)
  • CD8-Positive T-Lymphocytes (immunology)
  • Carcinoma, Non-Small-Cell Lung (immunology, metabolism, pathology, surgery)
  • Female
  • Follow-Up Studies
  • Humans
  • Lung Neoplasms (immunology, metabolism, pathology, surgery)
  • Lymphocytes, Tumor-Infiltrating (immunology)
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local (immunology, metabolism, pathology, surgery)
  • Neoplasm Staging
  • Programmed Cell Death 1 Receptor (immunology, metabolism)
  • Retrospective Studies
  • Survival Rate
  • Tumor Microenvironment (immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: