The Prognostic Significance of Programmed Death-Ligand 1 (PD-L1) in Skin Neoplasms: A Systematic Review and
Alireza Abdollahi1, Emad Mehrtash2, Bita Jafarzadeh1
1Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
International Journal of Surgical Pathology
|August 22, 2025
Summary
Programmed death-ligand 1 (PD-L1) expression has varied prognostic value in skin cancers. While not significantly impacting overall survival broadly, it predicts better outcomes in Merkel cell carcinoma but worse in others.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Programmed death-ligand 1 (PD-L1) is an immune checkpoint molecule with established therapeutic and prognostic roles.
- The prognostic significance of PD-L1 in various skin neoplasms is not fully understood and remains controversial.
Purpose of the Study:
- To systematically evaluate the prognostic value of PD-L1 expression in overall survival (OS) and disease-free survival (DFS) across different skin neoplasms.
Main Methods:
- A meta-analysis of 24 studies systematically searched from PubMed, Scopus, and Web of Science databases up to March 2025.
- Outcome measures included OS and DFS, with subgroup analyses conducted based on tumor type.
- Heterogeneity and publication bias were assessed using I² statistics and funnel plots.
Main Results:
- Overall, PD-L1 expression did not significantly correlate with OS (HR=0.89) or DFS (HR=0.86).
- Subgroup analysis revealed improved OS with PD-L1 expression in Merkel cell carcinoma (HR=0.39).
- PD-L1 predicted better DFS in melanoma and cutaneous squamous cell carcinoma, but worse DFS in cutaneous angiosarcoma and sebaceous gland carcinoma. PD-L1 also correlated with lymph node metastasis risk in squamous cell carcinoma (OR=5.33).
Conclusions:
- The prognostic impact of PD-L1 expression in skin neoplasms is highly subtype-specific.
- PD-L1 may indicate improved survival in certain skin cancers like Merkel cell carcinoma, while predicting poorer outcomes in others such as cutaneous angiosarcoma and sebaceous gland carcinoma.
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