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Updated: Aug 26, 2026

Immunohistochemical Staining of B7-H1 (PD-L1) on Paraffin-embedded Slides of Pancreatic Adenocarcinoma Tissue
Published on: January 3, 2013
Association between PD-1/PD-L1 Expression and Clinicopathological Parameters as well as Prognosis in Neuroendocrine
Qiming Zheng1,2,3,4, Xinyue Xie1, Qingjun Guo2
1Department of Liver Transplantation, First Central Hospital of Tianjin Medical University , Tianjin, China.
Abstract:
Neuroendocrine neoplasms (NENs) are a highly heterogeneous group of tumors originating from the neuroendocrine system, predominantly occurring in the gastrointestinal tract and lungs. This meta-analysis aimed to clarify the association of programmed death 1 (PD-1)/programmed death-ligand 1 (PD-L1) expression with clinicopathological parameters and prognosis in patients with digestive system NENs. A systematic literature search was performed in PubMed, Web of Science, Embase, the Cochrane Library, China National Knowledge Infrastructure (CNKI), Wanfang Database, and China BioMedical Literature Database (CBM) from each database's inception to February 2026. Eligible studies were analyzed using Stata 17.0 software, with 29 studies involving 2,633 patients included.Results showed no significant association between PD-1 expression and clinicopathological parameters or prognosis. In contrast, PD-L1 expression was closely correlated with high tumor grade (OR=2.73, 95%CI: 1.33-5.60; p=0.006) and pancreatic primary tumor site (OR=2.58, 95%CI: 1.21-5.52; p=0.014). Regarding prognosis, positive PD-L1 expression was associated with inferior overall survival (OS) in gastroenteropancreatic NENs (GEP-NENs) (HR=1.77, 95%CI: 1.25-2.51; p=0.001) but favorable OS in esophageal NENs (HR=0.60, 95%CI: 0.37-0.99; p=0.047). In conclusion, PD-L1 expression correlates with high tumor grade and pancreatic origin. It serves as a predictive biomarker for poor OS in GEP-NENs but favorable prognosis in esophageal NENs, highlighting the divergent prognostic value of the PD-1/PD-L1 axis across digestive system NEN subtypes. These findings provide hypothesis-generating evidence for the potential rationale of immune checkpoint inhibitors in high-grade or poorly differentiated GEP-NENs, although their clinical application requires further prospective validation.
