Programmed Death-Ligand 1 Expression in Muscle-Invasive Bladder Cancer Cystectomy Specimens and Lymph Node
Deborah Mukherji1, Mark N Jabbour2, Maya Saroufim2
1Department of Internal Medicine, Division of Hematology-Oncology, American University of Beirut Medical Center, Beirut, Lebanon.
Programmed death-1 (PD-1) ligand (PD-L1) expression was assessed in muscle-invasive bladder cancer. PD-L1 was found in tumor cells and immune cells, but expression differed between primary tumors and lymph node metastases.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- The programmed death-1 (PD-1) pathway is crucial for T-cell regulation and antitumor immunity.
- Monoclonal antibodies targeting PD-1/PD-L1 show promise in various cancers, with PD-L1 expression potentially predicting response.
- Understanding PD-L1 expression in muscle-invasive bladder cancer (MIBC) is key for selecting patients for PD-1 therapy.
Purpose of the Study:
- To determine the frequency of PD-L1 expression in MIBC and associated lymph node metastases.
- To evaluate PD-L1 as a biomarker for patient selection in PD-1-directed therapy.
Main Methods:
- Retrospective analysis of 52 radical cystectomy specimens from patients without prior chemotherapy.
- Immunohistochemistry using an anti-PD-L1 antibody (5H1 clone).
- PD-L1 positivity defined as ≥5% expression in tumor cells or immune cells.
Main Results:
- PD-L1 overexpression was observed in tumor cells of 9.6% (5/52) and immune cells of 32.7% (17/52) of MIBC specimens.
- Significant discordance in PD-L1 expression was noted between primary tumors and lymph node metastases.
- This highlights potential challenges in using archived tissue for biomarker assessment.
Conclusions:
- Standardized assays for PD-L1 expression are still needed.
- Discordance between primary and metastatic sites suggests that pre-treatment biopsies are essential for accurate biomarker assessment.
- Future studies should prioritize fresh tissue acquisition immediately before therapy initiation.
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