AI Article Synopsis

  • * It was found that 39.4% of patients had PD-L1 positive expression, which was linked to lower T cell activation (SI levels) and associated with the presence of mutations in 72.7% of patients.
  • * The research suggests that high levels of PD-L1, along with CD8+ expression and mutation status, may serve as significant prognostic indicators for survival in thyroid cancer patients, especially in relation to progression-free survival.

Article Abstract

In thyroid cancer, it has been suggested that PD-L1 overexpression is associated with some clinicopathological factors and prognosis. The aim of this study is to characterize the expression of PD-L1, the presence of the mutation, as well as cellular and humoral immunity in thyroid cancer, and to investigate the factors that predict the effectiveness of anti-PD-L1 antibody therapy. Blood samples were collected from 33 patients who were newly diagnosed with thyroid cancer after surgery or biopsy. PD-L1 expression, mutation, and CD8+ expression were examined by immunohistological staining using clinical thyroid cancer specimens. With a PD-L1 staining cut-off value of 1%, 13 (39.4%) patients were classified as PD-L1 positive. Stimulation Index (SI) is an indicator of T cell activation. PD-L1 expression was significantly correlated with low SI level ( = 0.046). Moreover, mutation was detected in 24 of the 33 (72.7%) patients, and was significantly associated with PD-L1 expression ( = 0.047). In addition, enhanced CD8+ expression was significantly associated with PD-L1 expression ( = 0.003). Multivariate analyses confirmed that high CRP levels ( = 0.039) were independently and significantly associated with poor progression-free survival. These findings suggest that elevated PD-L1 status can be a prognostic indicator for survival in patients with thyroid cancer when comprehensively assessed using the expression of CD8+, the presence of mutation and the patient's immune status.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341229PMC
http://dx.doi.org/10.3390/cancers15133449DOI Listing

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