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The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer

We investigated the correlation between Cyclooxygenase-2 (COX-2) expression and the tumor response in patients with cervical cancer that were treated with curative radiotherapy (RT). Fifty-seven patients with squamous cell carcinoma were treated with concurrent radiochemotherapy (CRCT, n=29) or RT a...

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Autores principales: Kang, Min Kyu, Park, Won, Choi, Yoon-La, Cho, Eun Yoon, Ahn, Geunghwan, Nam, HeeRim, Huh, Seung Jae, Ahn, Yong Chan, Lim, Do Hoon, Oh, Dong Ryul, Bae, Duk Soo, Kim, Byoung Gie
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775869/
https://www.ncbi.nlm.nih.gov/pubmed/19949677
http://dx.doi.org/10.3346/jkms.2009.24.6.1170
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author Kang, Min Kyu
Park, Won
Choi, Yoon-La
Cho, Eun Yoon
Ahn, Geunghwan
Nam, HeeRim
Huh, Seung Jae
Ahn, Yong Chan
Lim, Do Hoon
Oh, Dong Ryul
Bae, Duk Soo
Kim, Byoung Gie
author_facet Kang, Min Kyu
Park, Won
Choi, Yoon-La
Cho, Eun Yoon
Ahn, Geunghwan
Nam, HeeRim
Huh, Seung Jae
Ahn, Yong Chan
Lim, Do Hoon
Oh, Dong Ryul
Bae, Duk Soo
Kim, Byoung Gie
author_sort Kang, Min Kyu
collection PubMed
description We investigated the correlation between Cyclooxygenase-2 (COX-2) expression and the tumor response in patients with cervical cancer that were treated with curative radiotherapy (RT). Fifty-seven patients with squamous cell carcinoma were treated with concurrent radiochemotherapy (CRCT, n=29) or RT alone (n=28). The response of each patient was evaluated by three serial Magnetic Resonance Imaging examinations: before the start of RT, at four weeks after the start of RT (mid-RT) and at four weeks after the completion of RT (post-RT). Forty-three patients had positive COX-2 expression. The COX-2 negative patients achieved a higher rate of complete response (CR) at mid-RT than did the COX-2 positive patients (28.6% vs. 7.0%, P=0.054), but not at post-RT (64.3% vs. 69.8%). The initial tumor volume was a significant predictor of CR at mid-RT (P=0.003) and post-RT (P=0.004). The multivariate analysis showed that the initial tumor volume (at mid-RT and post-RT) and CRCT (at post-RT) were significant predictors of CR; however, the COX-2 expression was not. In conclusion, the COX-2 expression status has no significant correlation with the tumor response. Further studies on the changes in COX-2 expression levels during RT may be helpful for determination of its role in the tumor response to treatment and patient prognosis.
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spelling pubmed-27758692009-12-01 The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer Kang, Min Kyu Park, Won Choi, Yoon-La Cho, Eun Yoon Ahn, Geunghwan Nam, HeeRim Huh, Seung Jae Ahn, Yong Chan Lim, Do Hoon Oh, Dong Ryul Bae, Duk Soo Kim, Byoung Gie J Korean Med Sci Original Article We investigated the correlation between Cyclooxygenase-2 (COX-2) expression and the tumor response in patients with cervical cancer that were treated with curative radiotherapy (RT). Fifty-seven patients with squamous cell carcinoma were treated with concurrent radiochemotherapy (CRCT, n=29) or RT alone (n=28). The response of each patient was evaluated by three serial Magnetic Resonance Imaging examinations: before the start of RT, at four weeks after the start of RT (mid-RT) and at four weeks after the completion of RT (post-RT). Forty-three patients had positive COX-2 expression. The COX-2 negative patients achieved a higher rate of complete response (CR) at mid-RT than did the COX-2 positive patients (28.6% vs. 7.0%, P=0.054), but not at post-RT (64.3% vs. 69.8%). The initial tumor volume was a significant predictor of CR at mid-RT (P=0.003) and post-RT (P=0.004). The multivariate analysis showed that the initial tumor volume (at mid-RT and post-RT) and CRCT (at post-RT) were significant predictors of CR; however, the COX-2 expression was not. In conclusion, the COX-2 expression status has no significant correlation with the tumor response. Further studies on the changes in COX-2 expression levels during RT may be helpful for determination of its role in the tumor response to treatment and patient prognosis. The Korean Academy of Medical Sciences 2009-12 2009-11-09 /pmc/articles/PMC2775869/ /pubmed/19949677 http://dx.doi.org/10.3346/jkms.2009.24.6.1170 Text en Copyright © 2009 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kang, Min Kyu
Park, Won
Choi, Yoon-La
Cho, Eun Yoon
Ahn, Geunghwan
Nam, HeeRim
Huh, Seung Jae
Ahn, Yong Chan
Lim, Do Hoon
Oh, Dong Ryul
Bae, Duk Soo
Kim, Byoung Gie
The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer
title The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer
title_full The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer
title_fullStr The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer
title_full_unstemmed The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer
title_short The Effect of Cyclooxygenase-2 Expression on Tumor Volume Response in Patients Treated with Radiotherapy for Uterine Cervical Cancer
title_sort effect of cyclooxygenase-2 expression on tumor volume response in patients treated with radiotherapy for uterine cervical cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775869/
https://www.ncbi.nlm.nih.gov/pubmed/19949677
http://dx.doi.org/10.3346/jkms.2009.24.6.1170
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