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Long-term survival of endometrioid endometrial cancer patients

INTRODUCTION: To establish risk factors for onset and progression of endometrioid endometrial cancer still remains the aim of scientists. The aim of the study was to determine disease-free survival (DFS) and overall survival (OS) in women with endometrioid endometrial cancer. MATERIAL AND METHODS: A...

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Autores principales: Gottwald, Leszek, Pluta, Piotr, Piekarski, Janusz, Spych, Michał, Hendzel, Katarzyna, Topczewska-Tylinska, Katarzyna, Nejc, Dariusz, Bibik, Robert, Korczyński, Jerzy, Ciałkowska-Rysz, Aleksandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302708/
https://www.ncbi.nlm.nih.gov/pubmed/22427770
http://dx.doi.org/10.5114/aoms.2010.19305
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author Gottwald, Leszek
Pluta, Piotr
Piekarski, Janusz
Spych, Michał
Hendzel, Katarzyna
Topczewska-Tylinska, Katarzyna
Nejc, Dariusz
Bibik, Robert
Korczyński, Jerzy
Ciałkowska-Rysz, Aleksandra
author_facet Gottwald, Leszek
Pluta, Piotr
Piekarski, Janusz
Spych, Michał
Hendzel, Katarzyna
Topczewska-Tylinska, Katarzyna
Nejc, Dariusz
Bibik, Robert
Korczyński, Jerzy
Ciałkowska-Rysz, Aleksandra
author_sort Gottwald, Leszek
collection PubMed
description INTRODUCTION: To establish risk factors for onset and progression of endometrioid endometrial cancer still remains the aim of scientists. The aim of the study was to determine disease-free survival (DFS) and overall survival (OS) in women with endometrioid endometrial cancer. MATERIAL AND METHODS: A retrospective review of 142 patients with endometrioid endometrial cancer after surgery treated with adjuvant radiotherapy and/or chemotherapy in the Regional Cancer Centre in Lodz between 2002 and 2004 was performed. Clinical and pathological data were correlated with clinical outcome and survival. RESULTS: In 3 patients (2.1%) clinical progression was diagnosed during the treatment. In 23 patients (16.7%) after primary remission, relapse was diagnosed 2-56 months after treatment. DFS and OS were 81.7% and 83.1% respectively. Better DFS significantly correlated with larger number of pregnancies (> 1), stage I of the disease and optimal surgery. Lower stage of disease, pelvic lymph node dissection, optimal surgery and depth of myometrial infiltration ≤ 50% were independent prognostic factors for better OS. CONCLUSIONS: The results of our study provided significant evidence that early detection of endometrioid endometrial cancer enables optimal surgery. It reduces the indications for adjuvant therapy in stage I of the disease, and makes the prognosis significantly better. Other clinical and pathological factors such as numerous pregnancies, pelvic lymphadenectomy, and depth of myometrial infiltration, although important, are of less significance. Further prospective, randomized studies are necessary to prove the role of these factors.
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spelling pubmed-33027082012-03-16 Long-term survival of endometrioid endometrial cancer patients Gottwald, Leszek Pluta, Piotr Piekarski, Janusz Spych, Michał Hendzel, Katarzyna Topczewska-Tylinska, Katarzyna Nejc, Dariusz Bibik, Robert Korczyński, Jerzy Ciałkowska-Rysz, Aleksandra Arch Med Sci Clinical Research INTRODUCTION: To establish risk factors for onset and progression of endometrioid endometrial cancer still remains the aim of scientists. The aim of the study was to determine disease-free survival (DFS) and overall survival (OS) in women with endometrioid endometrial cancer. MATERIAL AND METHODS: A retrospective review of 142 patients with endometrioid endometrial cancer after surgery treated with adjuvant radiotherapy and/or chemotherapy in the Regional Cancer Centre in Lodz between 2002 and 2004 was performed. Clinical and pathological data were correlated with clinical outcome and survival. RESULTS: In 3 patients (2.1%) clinical progression was diagnosed during the treatment. In 23 patients (16.7%) after primary remission, relapse was diagnosed 2-56 months after treatment. DFS and OS were 81.7% and 83.1% respectively. Better DFS significantly correlated with larger number of pregnancies (> 1), stage I of the disease and optimal surgery. Lower stage of disease, pelvic lymph node dissection, optimal surgery and depth of myometrial infiltration ≤ 50% were independent prognostic factors for better OS. CONCLUSIONS: The results of our study provided significant evidence that early detection of endometrioid endometrial cancer enables optimal surgery. It reduces the indications for adjuvant therapy in stage I of the disease, and makes the prognosis significantly better. Other clinical and pathological factors such as numerous pregnancies, pelvic lymphadenectomy, and depth of myometrial infiltration, although important, are of less significance. Further prospective, randomized studies are necessary to prove the role of these factors. Termedia Publishing House 2010-12 2010-12-29 /pmc/articles/PMC3302708/ /pubmed/22427770 http://dx.doi.org/10.5114/aoms.2010.19305 Text en Copyright © 2010 Termedia & Banach 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 Clinical Research
Gottwald, Leszek
Pluta, Piotr
Piekarski, Janusz
Spych, Michał
Hendzel, Katarzyna
Topczewska-Tylinska, Katarzyna
Nejc, Dariusz
Bibik, Robert
Korczyński, Jerzy
Ciałkowska-Rysz, Aleksandra
Long-term survival of endometrioid endometrial cancer patients
title Long-term survival of endometrioid endometrial cancer patients
title_full Long-term survival of endometrioid endometrial cancer patients
title_fullStr Long-term survival of endometrioid endometrial cancer patients
title_full_unstemmed Long-term survival of endometrioid endometrial cancer patients
title_short Long-term survival of endometrioid endometrial cancer patients
title_sort long-term survival of endometrioid endometrial cancer patients
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302708/
https://www.ncbi.nlm.nih.gov/pubmed/22427770
http://dx.doi.org/10.5114/aoms.2010.19305
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