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Evaluation Challenges in the Validation of B7-H3 as Oral Tongue Cancer Prognosticator

Authors :
Rabeia Almahmoudi
Priscila Campioni Rodrigues
Elin Synnøve Hadler-Olsen
Inger-Heidi Bjerkli
Pirjo Åström
Sanna Toppila-Salmi
Anna Maria Wirsing
Ricardo D. Coletta
Tuula Salo
Ahmed Al-Samadi
Timo Paavonen
Aini Hyytiäinen
Meri Sieviläinen
Department of Oral and Maxillofacial Diseases
Clinicum
University of Helsinki
TRIMM - Translational Immunology Research Program
Research Programs Unit
Faculty of Medicine
Medicum
HUSLAB
HUS Inflammation Center
Department of Dermatology, Allergology and Venereology
Helsinki University Hospital Area
HUS Head and Neck Center
Tampere University
Department of Pathology
Clinical Medicine
Source :
Head and Neck Pathology
Publication Year :
2020

Abstract

B7-H3 was the only molecule identified with prognostic potential from a recent systematic review of the prognostic value of immune checkpoints in oral cancer. We aimed to validate this finding in a multicenter international cohort. We retrospectively retrieved 323 oral tongue squamous cell carcinoma (OTSCC) samples from three different countries (Brazil, Finland, and Norway) for immunostaining and scoring for B7-H3. We evaluated tumor immunogenicity by analyzing the amount of tumor-infiltrating lymphocytes and divided the tumors into immune hot and cold. To increase the reliability of the results, both digital and manual visual scoring were used. Survival curves were constructed based on the Kaplan-Meier method, and the Cox proportional hazard model was utilized for univariate and multivariate survival analysis. B7-H3 expression was not significantly associated with overall or disease-specific survival in the whole OTSCC cohort. When divided into immune hot and cold tumors, high B7-H3 expression was significantly associated with poor disease-specific and overall survival in the immune hot group, depending on the scoring method and the country of the cohort. This was achieved only in the univariate analysis. In conclusion, B7-H3 was a negative prognosticator for OTSCC patient survival in the subgroup of immune hot tumors, and was not validated as a prognosticator in the full cohort. Our findings suggest that the immune activity of the tumor should be considered when testing immune checkpoints as biomarkers. Electronic supplementary material The online version of this article (doi:10.1007/s12105-020-01222-3) contains supplementary material, which is available to authorized users.

Details

ISSN :
19360568
Volume :
15
Issue :
2
Database :
OpenAIRE
Journal :
Head and neck pathology
Accession number :
edsair.doi.dedup.....d30291317029efe98560a057ac2ed12a