Intraepithelial lymphocytes are indicators of better prognosis in surgically resected endometrioid-type endometrial carcinomas at early and advanced stages
Tumor-infiltrating lymphocytes (TILs) and tumor-associated macrophages (TAMs) may be useful prognostic indicators in endometrial cancer. However, standardized assessment methods and the prognostic roles of these cells in different stage groups are unclear. Formalin-fixed paraffin-embedded tissue sam...
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Veröffentlicht in: | BMC cancer 2022-04, Vol.22 (1), p.361-361, Article 361 |
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Zusammenfassung: | Tumor-infiltrating lymphocytes (TILs) and tumor-associated macrophages (TAMs) may be useful prognostic indicators in endometrial cancer. However, standardized assessment methods and the prognostic roles of these cells in different stage groups are unclear.
Formalin-fixed paraffin-embedded tissue samples of 107 endometrioid-type endometrial carcinomas (EECs) comprising 60 stage IB and 47 stage IIIC or IVB cases were evaluated. CD3
TILs, CD8
TILs, CD68
TAMs, and CD163
TAMs were detected by immunohistochemistry, and their densities were evaluated by semiquantitative and quantitative methods. TILs within tumor epithelial cell nests (E-TILs) and those within the stroma at the invasive front (S-TILs) were evaluated separately for CD3
and CD8
cells. The "TIL score" was defined as the sum of semiquantitative scores of CD3
E-TILs, CD3
S-TILs, CD8
E-TILs, and CD8
S-TILs. For TAMs, the area of CD68
and CD163
cells in the invasive margin were semiquantitatively and quantitatively evaluated. Clinicopathological and prognostic implications of TILs and TAMs in stage IB and IIIC/IVB EECs were examined by Cox univariate and multivariate analyses.
By Cox univariate analyses, semiquantitatively low CD3
E-TILs, low CD8
E-TILs, and low "TIL score" were significantly correlated with worse prognosis in stage IB patients (P = 0.011, 0.040, and 0.039, respectively). Likewise, low CD3
E-TILs and low CD8
E-TILs, by both semiquantitative (P = 0.011 and 0.0051) and quantitative evaluations (P |
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ISSN: | 1471-2407 1471-2407 |
DOI: | 10.1186/s12885-022-09363-0 |