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Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma

OBJECTIVES: The current study aims to quantify the growth rate of p16‐negative oral cavity squamous cell carcinoma, characterize causative relationships between demographic risk factors and tumor growth, and examine pathologic findings associated with the tumor growth rate at a tertiary care institu...

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Autores principales: Wihlidal, Jacob G. J., Tay, Keng Yeow, MacNeil, S. Danielle, Nichols, Anthony C., Fung, Kevin, Yoo, John H. J., Mendez, Adrian I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575115/
https://www.ncbi.nlm.nih.gov/pubmed/36258883
http://dx.doi.org/10.1002/lio2.831
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author Wihlidal, Jacob G. J.
Tay, Keng Yeow
MacNeil, S. Danielle
Nichols, Anthony C.
Fung, Kevin
Yoo, John H. J.
Mendez, Adrian I.
author_facet Wihlidal, Jacob G. J.
Tay, Keng Yeow
MacNeil, S. Danielle
Nichols, Anthony C.
Fung, Kevin
Yoo, John H. J.
Mendez, Adrian I.
author_sort Wihlidal, Jacob G. J.
collection PubMed
description OBJECTIVES: The current study aims to quantify the growth rate of p16‐negative oral cavity squamous cell carcinoma, characterize causative relationships between demographic risk factors and tumor growth, and examine pathologic findings associated with the tumor growth rate at a tertiary care institution. It is hypothesized that causative relationships will be drawn between the individual sociodemographic and pathologic factors and oral cavity p16‐negative squamous cell carcinoma growth rate. METHODS: Prospectively recruited participants, receiving surgical intervention only, were followed from initial staging CT scan to surgical resection. Interval growth was calculated in cm(3)/week. Demographic information including age, sex, smoking history, alcohol consumption history, previous all‐type malignancy, previous chemotherapy treatment, previous head or neck radiation exposure, and time interval elapsed between diagnosis and surgery was collected from each participant, and regression analysis was applied to determine causality. RESULTS: Summary statistics revealed a mean growth rate for the study sample of 1.385cm(3)/week. Statistically significant regression correlations were detected between tumor growth and alcohol consumption, origination at the retromolar trigone, and clinical nodal stage. CONCLUSIONS: Through a small prospective cohort sample, the current study suggests clinical associations between alcohol consumption, origination at the retromolar trigone, and clinical nodal stage with rate of tumor growth. Future work will validate these relationships in a larger patient cohort, and against stronger modeling techniques. LEVEL OF EVIDENCE: Prospective non‐random cohort design.
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spelling pubmed-95751152022-10-17 Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma Wihlidal, Jacob G. J. Tay, Keng Yeow MacNeil, S. Danielle Nichols, Anthony C. Fung, Kevin Yoo, John H. J. Mendez, Adrian I. Laryngoscope Investig Otolaryngol Head and Neck, and Tumor Biology OBJECTIVES: The current study aims to quantify the growth rate of p16‐negative oral cavity squamous cell carcinoma, characterize causative relationships between demographic risk factors and tumor growth, and examine pathologic findings associated with the tumor growth rate at a tertiary care institution. It is hypothesized that causative relationships will be drawn between the individual sociodemographic and pathologic factors and oral cavity p16‐negative squamous cell carcinoma growth rate. METHODS: Prospectively recruited participants, receiving surgical intervention only, were followed from initial staging CT scan to surgical resection. Interval growth was calculated in cm(3)/week. Demographic information including age, sex, smoking history, alcohol consumption history, previous all‐type malignancy, previous chemotherapy treatment, previous head or neck radiation exposure, and time interval elapsed between diagnosis and surgery was collected from each participant, and regression analysis was applied to determine causality. RESULTS: Summary statistics revealed a mean growth rate for the study sample of 1.385cm(3)/week. Statistically significant regression correlations were detected between tumor growth and alcohol consumption, origination at the retromolar trigone, and clinical nodal stage. CONCLUSIONS: Through a small prospective cohort sample, the current study suggests clinical associations between alcohol consumption, origination at the retromolar trigone, and clinical nodal stage with rate of tumor growth. Future work will validate these relationships in a larger patient cohort, and against stronger modeling techniques. LEVEL OF EVIDENCE: Prospective non‐random cohort design. John Wiley & Sons, Inc. 2022-08-16 /pmc/articles/PMC9575115/ /pubmed/36258883 http://dx.doi.org/10.1002/lio2.831 Text en © 2022 The Authors. Laryngoscope Investigative Otolaryngology published by Wiley Periodicals LLC on behalf of The Triological Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Head and Neck, and Tumor Biology
Wihlidal, Jacob G. J.
Tay, Keng Yeow
MacNeil, S. Danielle
Nichols, Anthony C.
Fung, Kevin
Yoo, John H. J.
Mendez, Adrian I.
Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
title Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
title_full Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
title_fullStr Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
title_full_unstemmed Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
title_short Demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
title_sort demographic and pathologic factor regression to a growth rate model of p16‐negative oral cavity squamous cell carcinoma
topic Head and Neck, and Tumor Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575115/
https://www.ncbi.nlm.nih.gov/pubmed/36258883
http://dx.doi.org/10.1002/lio2.831
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