AI Article Synopsis

  • The study assessed the effectiveness of one-step nucleic acid amplification (OSNA) compared to traditional pathological ultrastaging for detecting sentinel lymph node metastasis in early-stage endometrial cancer patients.
  • A total of 526 sentinel lymph nodes from 191 patients were analyzed, revealing that OSNA identified metastasis in 19.7% of cases, while ultrastaging detected it in only 8.8%.
  • OSNA demonstrated high sensitivity (92%) and resulted in a reclassification of disease stage for some patients, highlighting its potential to better determine the need for additional treatment upon diagnosis.

Article Abstract

The objective of this study was to evaluate the efficacy of one-step nucleic acid amplification (OSNA) for the detection of sentinel lymph node (SLN) metastasis compared to standard pathological ultrastaging in patients with early-stage endometrial cancer (EC). A total of 526 SLNs from 191 patients with EC were included in the study, and 379 SLNs (147 patients) were evaluated by both methods, OSNA and standard pathological ultrastaging. The central 1 mm portion of each lymph node was subjected to semi-serial sectioning at 200 μm intervals and examined by hematoxylin-eosin and immunohistochemistry with CK19; the remaining tissue was analyzed by OSNA for CK19 mRNA. The OSNA assay detected metastases in 19.7% of patients (14.9% micrometastasis and 4.8% macrometastasis), whereas pathological ultrastaging detected metastasis in 8.8% of patients (3.4% micrometastasis and 5.4% macrometastasis). Using the established cut-off value for detecting SLN metastasis by OSNA in EC (250 copies/μL), the sensitivity of the OSNA assay was 92%, specificity was 82%, diagnostic accuracy was 83%, and the negative predictive value was 99%. Discordant results between both methods were recorded in 20 patients (13.6%). OSNA resulted in an upstaging in 12 patients (8.2%). OSNA could aid in the identification of patients requiring adjuvant treatment at the time of diagnosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431061PMC
http://dx.doi.org/10.3390/cancers13174465DOI Listing

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