Determination of PD-L1 expression in effusions from mesothelioma by immuno-cytochemical staining
(2017) In Cancer Cytopathology 125(12). p.908-917- Abstract
BACKGROUND: Malignant mesothelioma (MM) is an aggressive, fatal tumor. Current therapeutic options only marginally improve survival. Programmed cell death ligand 1 (PD-L1) is a dominant mediator of immunosuppression, binding to programmed cell death 1 (PD-1). PD-L1 is up-regulated in cancer cells, and the PD-1/PD-L1 pathway plays a critical role in tumor immune evasion, thus providing a target for antitumor therapy. Further, a correlation between PD-L1 expression and prognosis has been reported. Studies performed on histological material have revealed expression of PD-L1 in MM, but no study has been performed on MM effusions thus far. METHODS: PD-L1 expression was determined by a commercially available antibody (clone 28-8) in 74... (More)
BACKGROUND: Malignant mesothelioma (MM) is an aggressive, fatal tumor. Current therapeutic options only marginally improve survival. Programmed cell death ligand 1 (PD-L1) is a dominant mediator of immunosuppression, binding to programmed cell death 1 (PD-1). PD-L1 is up-regulated in cancer cells, and the PD-1/PD-L1 pathway plays a critical role in tumor immune evasion, thus providing a target for antitumor therapy. Further, a correlation between PD-L1 expression and prognosis has been reported. Studies performed on histological material have revealed expression of PD-L1 in MM, but no study has been performed on MM effusions thus far. METHODS: PD-L1 expression was determined by a commercially available antibody (clone 28-8) in 74 formalin-fixed, paraffin-embedded cell blocks from body effusions obtained at diagnosis from patients with MM. The presence of MM cells was confirmed with CK5/6, calretinin, and EMA and the admixture of macrophages was assessed with CD68. Only cases containing more than 100 tumor cells were assessed. Membranous staining in tumor cells was considered positive. Survival time was calculated from the appearance of the first malignant effusion until death. RESULTS: Reactivity was observed in 23 of 61 (38%) of cases and was classified as ≥1%-5% (n = 9 cases), >5%-10% (n = 4 cases), >10%-50% (n = 4 cases), and >50% (n = 6 cases) positive cells. Survival times did not differ significantly between patients with PD-L1–positive and PD-L1–negative tumors. CONCLUSION: MM effusions are suitable for immune-cytochemical assessment of PD-L1 expression in malignant cells and the results are similar to those reported for histological specimens. Cancer Cytopathol 2017;125:908-17.
(Less)
- author
- Mansour, Mohammed S.I. LU ; Seidal, Tomas ; Mager, Ulrich ; Baigi, Amir LU ; Dobra, Katalin and Dejmek, Annika LU
- organization
- publishing date
- 2017-12
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- cytology, effusion, immunocytochemistry (ICC), malignant mesothelioma (MM), programmed cell death ligand 1 (PD-L1)
- in
- Cancer Cytopathology
- volume
- 125
- issue
- 12
- pages
- 10 pages
- publisher
- Wiley-Blackwell
- external identifiers
-
- scopus:85038083776
- pmid:28922567
- wos:000418130100005
- ISSN
- 1934-662X
- DOI
- 10.1002/cncy.21917
- project
- Improvement of diagnostic and prognostic cytopathology of lung cancer and malignant mesothelioma.
- language
- English
- LU publication?
- yes
- id
- 35dda173-e740-4423-8a70-252ca88f5341
- date added to LUP
- 2018-01-12 08:27:58
- date last changed
- 2025-01-08 03:02:06
@article{35dda173-e740-4423-8a70-252ca88f5341, abstract = {{<p>BACKGROUND: Malignant mesothelioma (MM) is an aggressive, fatal tumor. Current therapeutic options only marginally improve survival. Programmed cell death ligand 1 (PD-L1) is a dominant mediator of immunosuppression, binding to programmed cell death 1 (PD-1). PD-L1 is up-regulated in cancer cells, and the PD-1/PD-L1 pathway plays a critical role in tumor immune evasion, thus providing a target for antitumor therapy. Further, a correlation between PD-L1 expression and prognosis has been reported. Studies performed on histological material have revealed expression of PD-L1 in MM, but no study has been performed on MM effusions thus far. METHODS: PD-L1 expression was determined by a commercially available antibody (clone 28-8) in 74 formalin-fixed, paraffin-embedded cell blocks from body effusions obtained at diagnosis from patients with MM. The presence of MM cells was confirmed with CK5/6, calretinin, and EMA and the admixture of macrophages was assessed with CD68. Only cases containing more than 100 tumor cells were assessed. Membranous staining in tumor cells was considered positive. Survival time was calculated from the appearance of the first malignant effusion until death. RESULTS: Reactivity was observed in 23 of 61 (38%) of cases and was classified as ≥1%-5% (n = 9 cases), >5%-10% (n = 4 cases), >10%-50% (n = 4 cases), and >50% (n = 6 cases) positive cells. Survival times did not differ significantly between patients with PD-L1–positive and PD-L1–negative tumors. CONCLUSION: MM effusions are suitable for immune-cytochemical assessment of PD-L1 expression in malignant cells and the results are similar to those reported for histological specimens. Cancer Cytopathol 2017;125:908-17.</p>}}, author = {{Mansour, Mohammed S.I. and Seidal, Tomas and Mager, Ulrich and Baigi, Amir and Dobra, Katalin and Dejmek, Annika}}, issn = {{1934-662X}}, keywords = {{cytology; effusion; immunocytochemistry (ICC); malignant mesothelioma (MM); programmed cell death ligand 1 (PD-L1)}}, language = {{eng}}, number = {{12}}, pages = {{908--917}}, publisher = {{Wiley-Blackwell}}, series = {{Cancer Cytopathology}}, title = {{Determination of PD-L1 expression in effusions from mesothelioma by immuno-cytochemical staining}}, url = {{http://dx.doi.org/10.1002/cncy.21917}}, doi = {{10.1002/cncy.21917}}, volume = {{125}}, year = {{2017}}, }