Clinical Significance of Programmed Death Ligand-1 Expression in Esophageal Squamous Cell Carcinoma.


Journal

The Journal of surgical research
ISSN: 1095-8673
Titre abrégé: J Surg Res
Pays: United States
ID NLM: 0376340

Informations de publication

Date de publication:
07 2020
Historique:
received: 31 07 2019
revised: 08 02 2020
accepted: 16 02 2020
pubmed: 23 3 2020
medline: 15 9 2020
entrez: 23 3 2020
Statut: ppublish

Résumé

The aim of this study was to evaluate the association between the expression of programmed death ligand-1 (PD-L1) and clinical outcomes in patients with surgically resected esophageal squamous cell carcinoma (ESCC). We included 76 patients with primary ESCC who underwent surgical resection between January 2009 and December 2014 at National Defense Medical College Hospital. Using the tumor tissues, we evaluated PD-L1 expression in tumor cells and stromal reactive lymphocytes via immunohistochemistry. Furthermore, the relationship between PD-L1 expression and the clinicopathological status of patients with ESCC was investigated. PD-L1 expression in tumor cells was detected in 39.5% of the patients. In addition, 51.3% of the patients had PD-L1-positive stromal reactive lymphocytes and exhibited significantly longer overall survival than those with lack of PD-L1 expression in stromal reactive lymphocytes (median survival time, 56.0 versus 27.3 mo; log-rank test, P = 0.04). Patients with lack of PD-L1 expression in both tumor cells and stromal reactive lymphocytes showed worse overall survival than those with the PD-L1-positive expression in tumor cells and/or stromal reactive lymphocytes (P = 0.02). PD-L1-positive expression in stromal reactive lymphocytes, rather than in tumor cells, is associated with a longer survival in patients with ESCC.

Sections du résumé

BACKGROUND
The aim of this study was to evaluate the association between the expression of programmed death ligand-1 (PD-L1) and clinical outcomes in patients with surgically resected esophageal squamous cell carcinoma (ESCC).
MATERIALS AND METHODS
We included 76 patients with primary ESCC who underwent surgical resection between January 2009 and December 2014 at National Defense Medical College Hospital. Using the tumor tissues, we evaluated PD-L1 expression in tumor cells and stromal reactive lymphocytes via immunohistochemistry. Furthermore, the relationship between PD-L1 expression and the clinicopathological status of patients with ESCC was investigated.
RESULTS
PD-L1 expression in tumor cells was detected in 39.5% of the patients. In addition, 51.3% of the patients had PD-L1-positive stromal reactive lymphocytes and exhibited significantly longer overall survival than those with lack of PD-L1 expression in stromal reactive lymphocytes (median survival time, 56.0 versus 27.3 mo; log-rank test, P = 0.04). Patients with lack of PD-L1 expression in both tumor cells and stromal reactive lymphocytes showed worse overall survival than those with the PD-L1-positive expression in tumor cells and/or stromal reactive lymphocytes (P = 0.02).
CONCLUSIONS
PD-L1-positive expression in stromal reactive lymphocytes, rather than in tumor cells, is associated with a longer survival in patients with ESCC.

Identifiants

pubmed: 32200323
pii: S0022-4804(20)30102-5
doi: 10.1016/j.jss.2020.02.013
pii:
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

321-328

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Nozomi Ito (N)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama, Japan.

Hironori Tsujimoto (H)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama, Japan. Electronic address: tsujihi@ndmc.ac.jp.

Hiroyuki Horiguchi (H)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama, Japan.

Hideyuki Shimazaki (H)

Department of Pathology, National Defense Medical College, Tokorozawa, Saitama, Japan.

Hiromi Miyazaki (H)

Division of Traumatology, National Defense Medical College Research Institute, Tokorozawa, Saitama, Japan.

Daizoh Saitoh (D)

Division of Traumatology, National Defense Medical College Research Institute, Tokorozawa, Saitama, Japan.

Yoji Kishi (Y)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama, Japan.

Hideki Ueno (H)

Department of Surgery, National Defense Medical College, Tokorozawa, Saitama, Japan.

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Classifications MeSH