AI Article Synopsis

  • Uterine serous carcinomas (USC) make up 10% of uterine cancers but cause 40% of related deaths, highlighting the need for better molecular profiling for treatment.
  • A study of 53 USC patients analyzed genomic instability scores (GIS), tumor mutational burden (TMB), and tumor-infiltrating lymphocytes (TILs) to understand survival outcomes.
  • Results indicated that a higher TMB correlates with improved survival rates, while the GIS did not show a similar association; increased TILs were related to higher GIS scores.

Article Abstract

Background: Uterine serous carcinomas represent 10% of uterine carcinomas but account for nearly 40% of deaths from the disease. Improved molecular characterization of these tumors is instrumental in guiding targeted treatment and improving outcomes. This study assessed the genomic instability score (GIS), tumor mutational burden (TMB), and tumor-infiltrating lymphocytes (TILs) in patients with USC. Methods: A retrospective cohort study evaluated patients with USC following staging surgery. The GIS and TMB were determined from archived specimens. We evaluated the tumoral expression of CD3, CD4, CD8, FOXP3, and CD68 using immunohistochemistry. T-tests were used to assess associations of TILs with the GIS. Results: We evaluated 53 patients with USC. The median GIS was 31 (range: 0−52) and a higher GIS was not associated with progression-free (PFS) or overall survival (OS). The median TMB was 1.35 mt/Mb; patients with TMB > 1.35 mt/Mb had improved PFS and OS (p = 0.005; p = 0.002, respectively). Tumors with increased CD3+ and CD4+ immune cells had a higher mean GIS (p = 0.013, p = 0.002). Conclusions: TMB > 1.35 mt/Mb was associated with improved survival in USC patients, whereas the GIS was not. Lower TMB thresholds may provide prognostic value for less immunogenic tumors such as USC. In this limited cohort, we observed that increased TIL populations were correlated with a higher GIS.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856872PMC
http://dx.doi.org/10.3390/cancers15020528DOI Listing

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