# Rapid Automated Immunohistochemistry on Frozen Sections Enables Real‐Time Surgical Pathology Decisions

**Authors:** Camilla Christine Qvist, Mie Bruun Elmbak, Julie Smith, Josefine Staldgaard, Gry Lipczak, Majbritt Wagner‐Eckert, Tina Klitmøller Agander

PMC · DOI: 10.1111/apm.70145 · Apmis · 2026-02-03

## TL;DR

A new rapid immunohistochemistry method enables faster and more accurate intraoperative surgical decisions.

## Contribution

The study introduces and validates FFRA-IHC, a fast automated immunohistochemistry method for frozen sections.

## Key findings

- FFRA-IHC classified 25 out of 37 tumors not identifiable by H&E alone.
- All five ambiguous resection margins were resolved using FFRA-IHC.
- The method reduced hands-on time and showed efficiency gains over manual IHC.

## Abstract

Intraoperative frozen section (FS) analysis is critical in surgical pathology, but conventional hematoxylin and eosin (H&E) staining has limitations in poorly differentiated neoplasms and resection margins. Immunohistochemistry (IHC) provides higher diagnostic specificity, yet has traditionally been too time‐consuming for intraoperative urgency. This study aimed to optimize, validate, and evaluate Fast Frozen Rapid Automated Immunohistochemistry (FFRA‐IHC) using the Q‐Stain X Autostainer to improve surgical diagnostics. After optimization with antibodies CKAE, CK5, CK7, CD45, and Synaptophysin, 44 tissue samples from patients undergoing surgery at Rigshospitalet, Copenhagen, were analyzed by FS H&E, FFRA‐IHC, and standard formalin‐fixed paraffin‐embedded (FFPE) methods. Automated FFRA‐IHC showed high diagnostic accuracy and supported immediate clinical decision‐making: of 37 tumors not classifiable by FS H&E alone, 25 (68%) were classified into specific tumor types, and all five ambiguous resection margins were resolved. A cost–benefit analysis indicated efficiency gains with reduced hands‐on time compared to manual IHC. In conclusion, FFRA‐IHC demonstrated promising results for enhancing intraoperative diagnostics, leading to its implementation in the daily workflow at our department. Future studies should expand antibody panels and assess the broader clinical impact to further improve intra‐ and perioperative care.

## Full-text entities

- **Genes:** SYP (synaptophysin) [NCBI Gene 6855] {aka MRX96, MRXSYP, XLID96}, MLANA (melan-A) [NCBI Gene 2315] {aka MART-1, MART1}, KRT5 (keratin 5) [NCBI Gene 3852] {aka CK5, DDD, DDD1, EBS1, EBS2, EBS2A}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}
- **Diseases:** FS (MESH:D002062), metastasis (MESH:D009362), infiltrating ductal carcinoma (MESH:D044584), breast sclerosing adenosis (MESH:D005348), Ear-Nose-Throat (ENT) cancer (MESH:D004428), non-epithelial malignancies (MESH:D002277), SCC (MESH:D002294), benign lesions (MESH:D001932), DLBCL (MESH:D016403), glioblastoma (MESH:D005909), maxillary sinus lesion (MESH:D008444), meningioma (MESH:D008579), skin cancers (MESH:D012878), carcinogenic (MESH:D011230), head and neck tumor (MESH:D006258), lymphoma (MESH:D008223), neuroendocrine tumor (MESH:D018358), Carcinoma (MESH:D009369), melanoma (MESH:D008545)
- **Chemicals:** eosin (MESH:D004801), H&amp;E (MESH:D006371), ethanol (MESH:D000431), acetone (MESH:D000096), paraffin (MESH:D010232), Hematoxylin (MESH:D006416), formalin (MESH:D005557), 3,3'-diaminobenzidine (MESH:D015100), FFRA (-), sodium carbonate (MESH:C005686)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12865514/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12865514/full.md

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Source: https://tomesphere.com/paper/PMC12865514