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BMC Cancer ; 24(1): 1219, 2024 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-39354397

RESUMO

BACKGROUND: The study evaluated the prognostic impact of the immune microenvironment in LSCC with markers of major immune cells to identify the key determinants of short-term disease-free survival (ST DFS) and reveal factors related to disease progression. METHODS: The study cohort included 61 patients who underwent total laryngectomy, 83.6% of whom were male with a mean age of 64.3 years at the time of surgery. Twenty-five patients had long term DFS (over 5 years), 8 - had moderate DFS (between 2 and 5 years), and 28 had short-term DFS (less than 2 years). Immunohistochemical staining and evaluation were performed on samples collected after the laryngectomy. RESULTS: The samples' assessment revealed that the mean expression of all analysed markers was the highest both in stroma and the tumor compartment for short term DFS (ST DFS) patients. Analysis confirmed that a high stromal density of CD8 cells (p = 0.038) significantly correlated with DFS, and that the increased presence of CD57 cells (p = 0.021) was significantly associated with ST DFS. Moreover, the high density of CD68 cells in the tumor epithelial compartment had a negative prognostic impact on DFS (p = 0.032). Analysis of overall survival in the studied cohort with Kaplan-Meyer curves revealed that a high stromal density of CD68 cells was a significant negative predictor of OS (p = 0.008). CONCLUSIONS: The observed associations of CD68 cells infiltration with progression and prognosis in patients with LSCC provide potential screening and therapeutic opportunities for patients with unfavourable outcomes.


Assuntos
Neoplasias Laríngeas , Microambiente Tumoral , Humanos , Microambiente Tumoral/imunologia , Masculino , Neoplasias Laríngeas/patologia , Neoplasias Laríngeas/imunologia , Neoplasias Laríngeas/mortalidade , Neoplasias Laríngeas/cirurgia , Pessoa de Meia-Idade , Feminino , Idoso , Prognóstico , Laringectomia , Intervalo Livre de Doença , Biomarcadores Tumorais/metabolismo , Progressão da Doença , Imunomodulação , Antígenos CD/metabolismo , Antígenos de Diferenciação Mielomonocítica/metabolismo , Estadiamento de Neoplasias
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