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PD-1 and PD-L1 Expression in Endometrial Cancer: A Systematic Review of the Literature
Orazio De Tommasi1, Matteo Marchetti1, Marta Tripepi1
1Unit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35122 Padua, Italy.
Abstract:
Background/Objectives: Cancer immunotherapy through the use of PD-1/PD-L1 inhibitors have shown significant promise in endometrial carcinoma (EC), particularly in tumors with microsatellite instability (MSI) or mismatch repair deficiency (dMMR), present in approximately 30% of cases. This review evaluated PD-L1 and PD-1 expression as potential biomarkers for immunotherapy response in EC, focusing on their relationship with MSI status. Methods: A systematic review, adhering to PRISMA guidelines, analyzed studies from MEDLINE and Embase until February 2023 on PD-1/PD-L1 expression in EC stratified by MSI status, including diverse study designs but excluding conference abstracts, with independent screening, data extraction, and additional reference checks to ensure comprehensive coverage. Results: A systematic analysis of 10 studies found that PD-L1 expression was more frequently expressed in MSI tumors (49%) compared to microsatellite-stable tumors (MSS) (33.5%), while PD-1 was expressed in 58% of MSI cases and 48% of MSS cases. Despite these findings, the prognostic value of PD-L1/PD-1 remains uncertain, with conflicting results regarding their association with survival outcomes. PD-L1 expression varied across molecular subtypes, being highest in POLE-mutated tumors (76.56%) and serous carcinomas (73%). Differences in PD-L1 expression between primary and metastatic sites were also noted, complicating its use as a biomarker. Conclusions: The assessment of PD-L1 expression in EC could represent a valuable option for selecting patients who may benefit from immune checkpoint inhibitors (ICI), including those in the MSS cohort, thereby ensuring a more tailored and personalized treatment strategy.
Insights
PD-L1 expression is more common in microsatellite instability (MSI) endometrial tumors, suggesting it may help predict response to cancer immunotherapy, even in microsatellite-stable cases.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Cancer immunotherapy, specifically PD-1/PD-L1 inhibitors, shows promise for endometrial carcinoma (EC).
- This is particularly relevant for tumors with microsatellite instability (MSI) or mismatch repair deficiency (dMMR), found in about 30% of EC cases.
- PD-1 and PD-L1 expression are being investigated as biomarkers for predicting immunotherapy response in EC.
Purpose of the Study:
- To evaluate PD-L1 and PD-1 expression as potential biomarkers for immunotherapy response in endometrial carcinoma.
- To specifically analyze the relationship between PD-1/PD-L1 expression and microsatellite instability (MSI) status in EC.
Main Methods:
- A systematic review adhering to PRISMA guidelines was conducted.
- Studies were sourced from MEDLINE and Embase up to February 2023.
- Included studies analyzed PD-1/PD-L1 expression in EC, stratified by MSI status, with independent screening and data extraction.
Main Results:
- PD-L1 expression was higher in MSI tumors (49%) than microsatellite-stable (MSS) tumors (33.5%).
- PD-1 expression was observed in 58% of MSI cases and 48% of MSS cases.
- PD-L1 expression varied by molecular subtype (highest in POLE-mutated and serous carcinomas) and between primary and metastatic sites, complicating its biomarker utility.
Conclusions:
- Assessing PD-L1 expression in EC may help identify patients who can benefit from immune checkpoint inhibitors (ICI).
- This approach could extend to the microsatellite-stable (MSS) cohort, enabling personalized treatment strategies.
- Further research is needed to clarify the prognostic value of PD-L1/PD-1 expression for survival outcomes.
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