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Programmed cell death ligand-1 (PD-L1) expression in desmoid tumors: a retrospective study
A N Toksoz Yildirim1, M Akyurek, E Okay
1Department of Pathology, Istanbul Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Istanbul, Turkey. anuryldrm@gmail.com.
European Review for Medical and Pharmacological Sciences
|June 15, 2023
Summary
Desmoid tumors lack programmed death-ligand 1 (PD-L1) expression, suggesting anti-PD-1/PD-L1 therapy may not be effective. However, intratumoral lymphocytes showed PD-L1 positivity, warranting further investigation for desmoid tumor treatment.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Desmoid tumors are rare, locally aggressive fibroblastic proliferations lacking metastatic potential but with high recurrence rates.
- Genetic mutations in CTNNB1 or APC genes characterize desmoid tumors.
- While watchful waiting is suitable for asymptomatic cases, medical therapy is an option for symptomatic patients with high surgical morbidity risks.
Purpose of the Study:
- To assess the expression of programmed death-ligand 1 (PD-L1) in desmoid tumors.
- To evaluate the potential efficacy of anti-PD-1/PD-L1 therapy in desmoid tumor treatment.
Main Methods:
- Immunohistochemical staining for PD-L1 expression was performed on biopsy and resection samples from 18 desmoid tumor patients.
- Leica Bond® automated stainer was utilized for antibody staining.
Main Results:
- No desmoid tumor cells exhibited positive PD-L1 staining in any of the 18 specimens.
- All specimens contained intratumoral lymphocytes.
- Five of the specimens showed positive PD-L1 staining in intratumoral lymphocytes.
Conclusions:
- The absence of PD-L1 expression on desmoid tumor cells suggests that anti-PD-1/PD-L1 therapy is unlikely to be a beneficial treatment strategy.
- The presence of PD-L1 positive intratumoral lymphocytes indicates a potential area for future research in desmoid tumor immunotherapy.
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