AI Article Synopsis

  • Axillary lymph node status and sentinel lymph node (SLN) diagnosis are crucial for determining post-surgery treatment in breast cancer patients.
  • Recent advancements, including a rapid-immunohistochemical staining (R-IHC) method, allow for quick detection of SLN metastases in just 16 minutes during surgery.
  • In a study involving 160 SLNs from 108 patients, R-IHC demonstrated high sensitivity (95.2%) and specificity (100%), successfully identifying additional metastatic SLNs that standard methods missed.

Article Abstract

Axillary lymph node status and pathological diagnosis of sentinel lymph nodes (SLNs) is a prognostic factor that influences management of postoperative therapy. Recent reports indicate that one-step nucleic acid amplification and hematoxylin and eosin (HE)-stained frozen sections are effective for intraoperative diagnosis of SLNs. In the present study, we report a rapid-immunohistochemical staining (R-IHC) method that enables intraoperative detection of SLN metastases within 16 min using an anti-cytokeratin antibody. This is the first report on SLN diagnosis using R-IHC in patients with breast cancer. We prospectively examined 160 dissected SLNs from 108 breast cancer patients who underwent surgery at our institute. The dissected SLNs were sectioned and conventionally stained with HE or immunohistochemically labeled with anti-cytokeratin antibody using R-IHC procedures. Intraoperative R-IHC analyses were completed within 16 min, after which diagnoses were made by two pathologists. The total time required for intraoperative diagnosis was about 20 min. In this study series, R-IHC detected four metastatic SLNs that were undetected using conventional HE staining (4/20, 20.0%). Compared with subsequent permanent diagnosis, R-IHC offered 95.2% sensitivity and 100% specificity. These findings indicate R-IHC is a clinically applicable technique that enables precise and quick intraoperative detection of micro- and macrometastasis in breast cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459795PMC
http://dx.doi.org/10.1038/s41598-017-02883-xDOI Listing

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