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Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer

PURPOSE: To evaluate whether Point A asymmetry in low dose-rate (LDR) brachytherapy is associated with local control (LC), disease-free survival (DFS) and/or overall survival (OS). MATERIAL AND METHODS: A retrospective analysis of disease control and survival outcomes was conducted for patients who...

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Autores principales: Opfermann, Krisha J, Wahlquist, Amy, Watkins, John, Kohler, Matthew, Jenrette, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551371/
https://www.ncbi.nlm.nih.gov/pubmed/23346133
http://dx.doi.org/10.5114/jcb.2012.27945
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author Opfermann, Krisha J
Wahlquist, Amy
Watkins, John
Kohler, Matthew
Jenrette, Joseph
author_facet Opfermann, Krisha J
Wahlquist, Amy
Watkins, John
Kohler, Matthew
Jenrette, Joseph
author_sort Opfermann, Krisha J
collection PubMed
description PURPOSE: To evaluate whether Point A asymmetry in low dose-rate (LDR) brachytherapy is associated with local control (LC), disease-free survival (DFS) and/or overall survival (OS). MATERIAL AND METHODS: A retrospective analysis of disease control and survival outcomes was conducted for patients who underwent LDR brachytherapy for advanced cervical cancer. Institutional protocol entailed concurrent chemotherapy and whole pelvis radiotherapy (WPRT) over 5 weeks, followed by placement of Fletcher-Suit tandem and colpostat applicators at weeks 6 and 8. Objective Point A doses, 80-85 Gy, were accomplished by placement of Cesium-137 (Cs-137) sources. Cox proportional hazards regression models were used to assess associations between disease control and survival endpoints with variables of interest. RESULTS: The records of 50 patients with FIGO stage IB1-IVA cervical cancer undergoing LDR brachytherapy at our institution were identified. Thirty of these patients had asymmetry > 2.5%, and 11 patients had asymmetry > 5%. At a median survivor follow-up of 20.25 months, 15 patients had experienced disease failure (including 5 cervical/vaginal apex only failures and 2 failures encompassing the local site). Right/left dose asymmetry at Point A was associated with statistically significantly inferior LC (p = 0.035) and inferior DFS (p = 0.011) for patients with mean Point A dose of > 80 Gy. Insufficient evidence existed to conclude an association with OS. CONCLUSIONS: LDR brachytherapy may be associated with clinically significant dose asymmetry. The present study demonstrates that patients with Point A asymmetry have a higher risk of failure for DFS and LC.
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spelling pubmed-35513712013-01-23 Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer Opfermann, Krisha J Wahlquist, Amy Watkins, John Kohler, Matthew Jenrette, Joseph J Contemp Brachytherapy Original Paper PURPOSE: To evaluate whether Point A asymmetry in low dose-rate (LDR) brachytherapy is associated with local control (LC), disease-free survival (DFS) and/or overall survival (OS). MATERIAL AND METHODS: A retrospective analysis of disease control and survival outcomes was conducted for patients who underwent LDR brachytherapy for advanced cervical cancer. Institutional protocol entailed concurrent chemotherapy and whole pelvis radiotherapy (WPRT) over 5 weeks, followed by placement of Fletcher-Suit tandem and colpostat applicators at weeks 6 and 8. Objective Point A doses, 80-85 Gy, were accomplished by placement of Cesium-137 (Cs-137) sources. Cox proportional hazards regression models were used to assess associations between disease control and survival endpoints with variables of interest. RESULTS: The records of 50 patients with FIGO stage IB1-IVA cervical cancer undergoing LDR brachytherapy at our institution were identified. Thirty of these patients had asymmetry > 2.5%, and 11 patients had asymmetry > 5%. At a median survivor follow-up of 20.25 months, 15 patients had experienced disease failure (including 5 cervical/vaginal apex only failures and 2 failures encompassing the local site). Right/left dose asymmetry at Point A was associated with statistically significantly inferior LC (p = 0.035) and inferior DFS (p = 0.011) for patients with mean Point A dose of > 80 Gy. Insufficient evidence existed to conclude an association with OS. CONCLUSIONS: LDR brachytherapy may be associated with clinically significant dose asymmetry. The present study demonstrates that patients with Point A asymmetry have a higher risk of failure for DFS and LC. Termedia Publishing House 2012-03-30 2012-03 /pmc/articles/PMC3551371/ /pubmed/23346133 http://dx.doi.org/10.5114/jcb.2012.27945 Text en Copyright © 2012 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Opfermann, Krisha J
Wahlquist, Amy
Watkins, John
Kohler, Matthew
Jenrette, Joseph
Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer
title Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer
title_full Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer
title_fullStr Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer
title_full_unstemmed Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer
title_short Impact of point A asymmetry on local control and survival for low dose-rate (LDR) brachytherapy in cervical cancer
title_sort impact of point a asymmetry on local control and survival for low dose-rate (ldr) brachytherapy in cervical cancer
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551371/
https://www.ncbi.nlm.nih.gov/pubmed/23346133
http://dx.doi.org/10.5114/jcb.2012.27945
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