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Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma

OBJECTIVE: : Oral squamous-cell carcinoma (OSCC) accounts for >90% of oral cancers affecting adults mostly between the fourth to seventh decades of life. The most common OSCC treatment is concomitant chemoradiotherapy (CCRT) having both loco-regional and distant control, but CCRT has acute and ch...

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Autores principales: Minhas, Sadia, Kashif, Muhammad, Altaf, Wasif, Afzal, Nadeem, Nagi, Abdul Hanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese Anti-Cancer Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444929/
https://www.ncbi.nlm.nih.gov/pubmed/28607808
http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0096
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author Minhas, Sadia
Kashif, Muhammad
Altaf, Wasif
Afzal, Nadeem
Nagi, Abdul Hanan
author_facet Minhas, Sadia
Kashif, Muhammad
Altaf, Wasif
Afzal, Nadeem
Nagi, Abdul Hanan
author_sort Minhas, Sadia
collection PubMed
description OBJECTIVE: : Oral squamous-cell carcinoma (OSCC) accounts for >90% of oral cancers affecting adults mostly between the fourth to seventh decades of life. The most common OSCC treatment is concomitant chemoradiotherapy (CCRT) having both loco-regional and distant control, but CCRT has acute and chronic toxic effects on adjacent normal tissue. This study aimed to determine the side effects of CCRT on the oral mucosa and to characterize the clinicopathology of oral lesions in patients with OSCC. METHODS: This descriptive, cross-sectional study was certified by the Ethical Review Committee (UHS/Education/126-12/2728) of the University of Health Sciences, Lahore, Pakistan. OSSC patients (n=81) with various histological subtypes, grades, and stages were recruited, and findings on their oral examination were recorded. These patients received 70, 90, and 119 Gy of radiotherapy dosages in combination with the chemotherapy drugs cisplatin and 5-fluorouracil. Data were analyzed using SPSS 20.0. RESULTS: : The most common presentation of OSCC was a nonhealing ulcer (63%) involving tongue (55.6%). Clinical findings included mucositis (92.6%) and xerostomia of mild, moderate, and severe degrees in 11.1%, 46.9%, and 35.8% cases, respectively. Ulcers (87.7%), palpable lymph nodes (64.2%), limited mouth opening (64.2%) and fistula (40.7%) were also observed. In females, the association of radiotherapy dosage with limited mouth opening, xerostomia, and histological grading was statistically significant (P<0.05). The association of chemotherapy drugs with xerostomia (P=0.003) was also statistically significant. CONCLUSIONS: : CCRT induced mucositis, xerostomia, and trismus in patients with OSCC.
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spelling pubmed-54449292017-06-12 Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma Minhas, Sadia Kashif, Muhammad Altaf, Wasif Afzal, Nadeem Nagi, Abdul Hanan Cancer Biol Med Original Article OBJECTIVE: : Oral squamous-cell carcinoma (OSCC) accounts for >90% of oral cancers affecting adults mostly between the fourth to seventh decades of life. The most common OSCC treatment is concomitant chemoradiotherapy (CCRT) having both loco-regional and distant control, but CCRT has acute and chronic toxic effects on adjacent normal tissue. This study aimed to determine the side effects of CCRT on the oral mucosa and to characterize the clinicopathology of oral lesions in patients with OSCC. METHODS: This descriptive, cross-sectional study was certified by the Ethical Review Committee (UHS/Education/126-12/2728) of the University of Health Sciences, Lahore, Pakistan. OSSC patients (n=81) with various histological subtypes, grades, and stages were recruited, and findings on their oral examination were recorded. These patients received 70, 90, and 119 Gy of radiotherapy dosages in combination with the chemotherapy drugs cisplatin and 5-fluorouracil. Data were analyzed using SPSS 20.0. RESULTS: : The most common presentation of OSCC was a nonhealing ulcer (63%) involving tongue (55.6%). Clinical findings included mucositis (92.6%) and xerostomia of mild, moderate, and severe degrees in 11.1%, 46.9%, and 35.8% cases, respectively. Ulcers (87.7%), palpable lymph nodes (64.2%), limited mouth opening (64.2%) and fistula (40.7%) were also observed. In females, the association of radiotherapy dosage with limited mouth opening, xerostomia, and histological grading was statistically significant (P<0.05). The association of chemotherapy drugs with xerostomia (P=0.003) was also statistically significant. CONCLUSIONS: : CCRT induced mucositis, xerostomia, and trismus in patients with OSCC. Chinese Anti-Cancer Association 2017-05 /pmc/articles/PMC5444929/ /pubmed/28607808 http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0096 Text en Copyright 2017 Cancer Biology & Medicine http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Minhas, Sadia
Kashif, Muhammad
Altaf, Wasif
Afzal, Nadeem
Nagi, Abdul Hanan
Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
title Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
title_full Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
title_fullStr Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
title_full_unstemmed Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
title_short Concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
title_sort concomitant-chemoradiotherapy-associated oral lesions in patients with oral squamous-cell carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444929/
https://www.ncbi.nlm.nih.gov/pubmed/28607808
http://dx.doi.org/10.20892/j.issn.2095-3941.2016.0096
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