Evidence map›Paper›PMID 41558098›Full record

ArticleOral oncology2026

Accuracy of frozen section for HPV-Associated squamous cell carcinoma of unknown primary.

Sindhura Sridhar, Annie Moroco, Shravan Gowrishankar, Mitra Mehrad, Kim Ely, James S Lewis, Madalina Tuluc, Stacey Gargano, Melanie Hicks, Kyle Mannion and 5 more

Abstract read
In one paragraph

Article in Oral oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Sindhura SridharVanderbilt University Medical Center, Department of Otolaryngology - Head and Neck Surgery, 1215 21(st) Ave. S., Nashville, TN 37232, United States.
Annie MorocoThomas Jefferson University, Department of Otolaryngology - Head and Neck Surgery, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
Shravan GowrishankarVanderbilt University Medical Center, Department of Otolaryngology - Head and Neck Surgery, 1215 21(st) Ave. S., Nashville, TN 37232, United States.
Mitra MehradVanderbilt University Medical Center, Department of Pathology, Microbiology, and Immunology, 1211 Medical Center Drive, Nashville, TN 37232, United States.
Kim ElyVanderbilt University Medical Center, Department of Pathology, Microbiology, and Immunology, 1211 Medical Center Drive, Nashville, TN 37232, United States.
James S LewisVanderbilt University Medical Center, Department of Pathology, Microbiology, and Immunology, 1211 Medical Center Drive, Nashville, TN 37232, United States; Mayo Clinic Arizona, Department of Laboratory Medicine and Pathology, 5777 E Mayo Blvd, Phoenix, AZ 85054, United States.
Madalina TulucThomas Jefferson University, Department of Pathology and Genomic Medicine, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
Stacey GarganoThomas Jefferson University, Department of Pathology and Genomic Medicine, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
Melanie HicksVanderbilt University Medical Center, Department of Otolaryngology - Head and Neck Surgery, 1215 21(st) Ave. S., Nashville, TN 37232, United States.
Kyle MannionVanderbilt University Medical Center, Department of Otolaryngology - Head and Neck Surgery, 1215 21(st) Ave. S., Nashville, TN 37232, United States.
Arielle G ThalThomas Jefferson University, Department of Otolaryngology - Head and Neck Surgery, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
Adam J LuginbuhlThomas Jefferson University, Department of Otolaryngology - Head and Neck Surgery, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
Joseph M CurryThomas Jefferson University, Department of Otolaryngology - Head and Neck Surgery, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
David M CognettiThomas Jefferson University, Department of Otolaryngology - Head and Neck Surgery, 111 S. 11(th) St., Philadelphia, PA 19107, United States.
Michael C TopfVanderbilt University Medical Center, Department of Otolaryngology - Head and Neck Surgery, 1215 21(st) Ave. S., Nashville, TN 37232, United States. Electronic address: Michael.topf@vumc.org.

Funding

Vanderbilt Clinical Oncology Research Career Development ProgramK12CA090625 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Debra L. Friedman, Paula Jill Hurley · 2001 to 2026
$16.9M
Augmented Reality to Guide Head and Neck Cancer SurgeryK08CA293255 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Michael Topf · 2024 to 2026
$645k
NCI NIH HHS K08 CA293255NCI NIH HHS K12 CA090625
6 · The paper itself

Abstract

introductionCurrent guidelines for the management of metastatic squamous cell carcinoma of unknown primary (SCCUP) recommend submission of suspicious primary sites for frozen section analysis (FSA). This study aims to investigate the diagnostic accuracy of FSA for identification of HPV-associated SCCUP.

methodsA retrospective cohort study of patients with biopsy-proven p16-positive SCCUP who underwent diagnostic operation at two tertiary care institutions was performed. Sensitivity, specificity, PPV, and NPV of diagnostic FSA were assessed.

results77 patients were included in analysis. 66 patients underwent definitive TORS (diagnostic TORS operation with subsequent neck dissection after identification of the occult primary tumor), 7 patients underwent diagnostic TORS (TORS to identify occult primary tumor, no neck dissection), and 4 patients underwent direct laryngoscopy and biopsy only. Primary tumors were identified in 63 patients (82%) with a mean tumor size of 1.1 cm. There was no significant difference in size between patients whose tumor was identified on FSA (mean 1.1 cm) and on permanent only (mean 0.9 cm) (p = 0.26). The sensitivity, specificity, PPV, and NPV of FSA for SCCUP was 86%, 100%, 100%, and 86%, respectively. Diagnostic frozen specimens included 52 direct laryngoscopy biopsies and 69 TORS excisions. In the biopsies, sensitivity was 100% and NPV was 100%, whereas in the TORS-excised specimens, sensitivity was 77% and NPV was 77%.

conclusionsIn this case series of 77 patients with SCCUP, the sensitivity and NPV of FSA for identification of the primary tumor was over 85%. FSA is valuable during diagnostic operation for SCCUP.

Indexed as

Carcinoma, Squamous CellFrozen SectionsHuman Papillomavirus VirusesNeoplasms, Unknown PrimaryPapillomavirus InfectionsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesSensitivity and Specificity

Identifiers

PMID41558098
PMCPMC13378440

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.