PD-L1 Status in Tenosynovial Giant Cell Tumors

dc.authorid0000-0003-1708-0003
dc.authorid0000-0002-5910-0829
dc.authorid0000-0002-4907-8840
dc.authorid0000-0003-2443-2505
dc.contributor.authorZenginkinet, Tulay
dc.contributor.authorFaruq, Abdullahi Umar
dc.contributor.authorYildirim, Ayse Nur Toksoz
dc.contributor.authorIyetin, Yusuf
dc.contributor.authorOzturan, Burak
dc.contributor.authorOkay, Erhan
dc.contributor.authorCelik, Aykut
dc.date.accessioned2025-05-10T19:36:54Z
dc.date.issued2022
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground and Objectives: Tenosynovial giant cell tumors (TSGCTs) are benign soft tissue tumors that are divided into localized- and diffuse-type tumors, according to the World Health Organization classification of soft tissue tumours. The diffuse-type TSGCT sometimes behave aggressively and poses treatment challenges especially in patients with neurovascular involvement. Symptomatic patients who are not good candidates for surgery due to high morbidity risk may benefit from medical therapy. Objectives: Drugs that target programmed death ligand 1 (PD-L1) are among a new generation of medical therapy options, which, recently, have been explored and have displayed promising results in various cancer types; therefore, we aimed to investigate the PD-L1 status of TSGCTs as a possible therapeutic target. Materials and Methods: We assessed the PD-L1 status of 20 patients (15 men and 5 women, median age = 39 years) that had been diagnosed with TSGCTs in a single institution, between 2018 and 2020. The patients had localized- (n = 7) and diffuse-type (n = 13) TSGCTs. Formalin-fixed paraffin-embedded (FFPE) blocks were retrospectively retrieved from the pathology department. An immunohistochemical analysis was performed in sections of 3 micron thickness from these blocks. Results: Seventy-five percent of our patients with TSGCTs were immunopositive to PD-L1 staining. Conclusions: Taking into consideration the high positivity rate of PD-L1 staining in TSGCTs, PD-L1 blockage may be used as a valuable medical treatment for TSGCTs; however, further studies are needed.
dc.identifier.doi10.3390/medicina58091270
dc.identifier.issn1010-660X
dc.identifier.issn1648-9144
dc.identifier.issue9
dc.identifier.pmid36143947
dc.identifier.scopus2-s2.0-85138402107
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/medicina58091270
dc.identifier.urihttps://hdl.handle.net/20.500.14730/9339
dc.identifier.volume58
dc.identifier.wosWOS:000856778200001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofMedicina-Lithuania
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjecttenosynovial giant cell tumor
dc.subjectPD-1
dc.subjectPD-L1
dc.subjectimmunohistochemistry
dc.titlePD-L1 Status in Tenosynovial Giant Cell Tumors
dc.typeArticle

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