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Early Prediction of Oral Cancer by S100A7 Immunohistochemistry Signature-based Assessment

A Multi-Centre Prospective Community-Based Observational Study on Prediction of Malignant Progression of Clinically Suspicious Oral Lesions with STRATICYTE

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04622462
Enrollment
500
Registered
2020-11-10
Start date
2015-03-12
Completion date
2026-12-31
Last updated
2024-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral Neoplasm

Keywords

Leukoplakia, Erythroplakia, Erythroleukoplakia, Lesion, Oral Epithelial Dysplasia, S100A7 Biomarker, S100A7 Immunohistochemistry Signature-based, Early Diagnosis, STRATICYTE, Oral Neoplasia, Oral Epithelial Atypia, Hyperplasia, Hyperkeratosis, Oral Squamous Cell Carcinoma, Oral Cancer, Potentially Premalignant Oral Epithelial Lesion, OPMD, Mild Dysplasia, Moderate Dysplasia, Severe Dysplasia, Low-grade Dysplasia, High-grade Dysplasia, Personalized Medicine, Predictive Assay, Whole Slide Imaging, Computational Pathology, Digital Pathology, Artificial Intelligence, Machine Learning, OPML, Oral Potentially Malignant Disorder, Oral Potentially Malignant Lesion

Brief summary

The purpose of this observational study is to evaluate the utility of the S100A7 immunohistochemistry signature-based assessment - STRATICYTE - in determining the risk of progression to cancer of clinically suspicious oral lesions.

Detailed description

Background: The standard of care for potentially premalignant oral epithelial lesion (PPOEL) risk assessment for progression to cancer is dysplasia grading by histopathology. With significant overlap between dysplasia grades and high inter- and intra-observer variations, dysplasia grading alone has been shown to be inadequate as a prognostic tool. To investigate the utility of the S100A7 immunohistochemistry signature-based assessment - STRATICYTE - in the early diagnosis of invasive oral cancer, a prospective multi-center observational study was designed with specimens obtained from community-based practices. Methods: Patients that qualify to enroll in the study will be assessed for both standard of care histopathological assessment for dysplasia grade and STRATICYTE risk assessment, and followed for up to 60 months (from initial biopsy) to determine the outcome of their oral lesion(s).

Interventions

PROCEDUREStandard of Care Histopathology

Assessment for mild, moderate, or severe dysplasia, and risk of progression to oral cancer

PROCEDURESTRATICYTE Assessment

Assessment for risk of progression to oral cancer

Sponsors

Proteocyte Diagnostics Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Any clinically suspicious lesion biopsied to rule-out oral epithelial dysplasia/oral squamous cell carcinoma

Exclusion criteria

* Biopsied lesion with or without dysplasia concomitant with oral squamous cell carcinoma at initial biopsy

Design outcomes

Primary

MeasureTime frameDescription
Malignant Transformation Rate: Dysplasia60 monthsCancer progression rate in patients with oral neoplasia with dysplasia and STRATICYTE Low-Risk or Elevated Risk

Secondary

MeasureTime frameDescription
Malignant Transformation Rate: No Dysplasia60 monthsCancer progression rate in patients with oral neoplasia without dysplasia and STRATICYTE Low-Risk or Elevated-Risk
Recurrence Rate60 monthsRecurrence rate in patients with oral neoplasia with or without dysplasia and STRATICYTE Low-Risk or Elevated-Risk

Countries

Canada

Contacts

Primary ContactJason Hwang, PhD
jhwang@proteocyte.com(647) 255-1370
Backup ContactMark Darling, MSc, MChD
mark.darling@schulich.uwo.ca(519) 661-2111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026