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PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study

BACKGROUND: Endometrial carcinoma is the most common gynaecologic malignancy in industrialised countries and the incidence is still rising. Primary treatment is based on preoperative risk classification and consists in most cases of hysterectomy with bilateral salpingo-oophorectomy. In patients with...

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Autores principales: Visser, Nicole C. M., Bulten, Johan, van der Wurff, Anneke A. M., Boss, Erik A., Bronkhorst, Carolien M., Feijen, Harrie W. H., Haartsen, Joke E., van Herk, Hilde A. D. M., de Kievit, Ineke M., Klinkhamer, Paul J. J. M., Pijlman, Brenda M., Snijders, Marc P. M. L., Vandenput, Ingrid, Vos, M. Caroline, de Wit, Peter E. J., van de Poll-Franse, Lonneke V., Massuger, Leon F.A.G., Pijnenborg, Johanna M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485884/
https://www.ncbi.nlm.nih.gov/pubmed/26123742
http://dx.doi.org/10.1186/s12885-015-1487-3
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author Visser, Nicole C. M.
Bulten, Johan
van der Wurff, Anneke A. M.
Boss, Erik A.
Bronkhorst, Carolien M.
Feijen, Harrie W. H.
Haartsen, Joke E.
van Herk, Hilde A. D. M.
de Kievit, Ineke M.
Klinkhamer, Paul J. J. M.
Pijlman, Brenda M.
Snijders, Marc P. M. L.
Vandenput, Ingrid
Vos, M. Caroline
de Wit, Peter E. J.
van de Poll-Franse, Lonneke V.
Massuger, Leon F.A.G.
Pijnenborg, Johanna M. A.
author_facet Visser, Nicole C. M.
Bulten, Johan
van der Wurff, Anneke A. M.
Boss, Erik A.
Bronkhorst, Carolien M.
Feijen, Harrie W. H.
Haartsen, Joke E.
van Herk, Hilde A. D. M.
de Kievit, Ineke M.
Klinkhamer, Paul J. J. M.
Pijlman, Brenda M.
Snijders, Marc P. M. L.
Vandenput, Ingrid
Vos, M. Caroline
de Wit, Peter E. J.
van de Poll-Franse, Lonneke V.
Massuger, Leon F.A.G.
Pijnenborg, Johanna M. A.
author_sort Visser, Nicole C. M.
collection PubMed
description BACKGROUND: Endometrial carcinoma is the most common gynaecologic malignancy in industrialised countries and the incidence is still rising. Primary treatment is based on preoperative risk classification and consists in most cases of hysterectomy with bilateral salpingo-oophorectomy. In patients with serous and clear cell histology a complete surgical staging is mandatory. However, in routine clinical practice final histology regularly does not correspond with the preoperative histological diagnosis. This results in both over and under treatment. METHODS/DESIGN: The aim of this multicentre, prospective cohort study is to select a panel of prognostic biomarkers to improve preoperative diagnosis of endometrial carcinoma in order to identify those patients that need extended surgery and/or additional treatment. Additionally, we will determine whether incorporation of cervical cytology and comorbidity could improve this preoperative risk classification. All patients treated for endometrial carcinoma in the participating hospitals from September 2011 till December 2013 are included. Patient characteristics, as well as comorbidity are registered. Patients without preoperative histology, history of hysterectomy and/or endometrial carcinoma or no surgical treatment including hysterectomy are excluded. The preoperative histology and final pathology will be reviewed and compared by expert pathologists. Additional immunohistochemical analysis of IMP3, p53, ER, PR, MLH1, PTEN, beta-catenin, p16, Ki-67, stathmin, ARID1A and L1CAM will be performed. Preoperative histology will be compared with the final pathology results. Follow-up will be at least 24 months to determine risk factors for recurrence and outcome. DISCUSSION: This study is designed to improve surgical treatment of endometrial carcinoma patients. A total of 432 endometrial carcinoma patients were enrolled between 2011 and 2013. Follow-up will be completed in 2015. Preoperative histology will be evaluated systematically and background endometrium will be classified. This is the first study incorporating immunohistochemistry, cervical cytology and comorbidity to define the optimal panel of prognostic biomarkers that contribute in clinical decision making in the management of endometrial carcinoma. TRIAL REGISTRATION: Netherlands Trial Register number NTR3503
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spelling pubmed-44858842015-07-01 PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study Visser, Nicole C. M. Bulten, Johan van der Wurff, Anneke A. M. Boss, Erik A. Bronkhorst, Carolien M. Feijen, Harrie W. H. Haartsen, Joke E. van Herk, Hilde A. D. M. de Kievit, Ineke M. Klinkhamer, Paul J. J. M. Pijlman, Brenda M. Snijders, Marc P. M. L. Vandenput, Ingrid Vos, M. Caroline de Wit, Peter E. J. van de Poll-Franse, Lonneke V. Massuger, Leon F.A.G. Pijnenborg, Johanna M. A. BMC Cancer Study Protocol BACKGROUND: Endometrial carcinoma is the most common gynaecologic malignancy in industrialised countries and the incidence is still rising. Primary treatment is based on preoperative risk classification and consists in most cases of hysterectomy with bilateral salpingo-oophorectomy. In patients with serous and clear cell histology a complete surgical staging is mandatory. However, in routine clinical practice final histology regularly does not correspond with the preoperative histological diagnosis. This results in both over and under treatment. METHODS/DESIGN: The aim of this multicentre, prospective cohort study is to select a panel of prognostic biomarkers to improve preoperative diagnosis of endometrial carcinoma in order to identify those patients that need extended surgery and/or additional treatment. Additionally, we will determine whether incorporation of cervical cytology and comorbidity could improve this preoperative risk classification. All patients treated for endometrial carcinoma in the participating hospitals from September 2011 till December 2013 are included. Patient characteristics, as well as comorbidity are registered. Patients without preoperative histology, history of hysterectomy and/or endometrial carcinoma or no surgical treatment including hysterectomy are excluded. The preoperative histology and final pathology will be reviewed and compared by expert pathologists. Additional immunohistochemical analysis of IMP3, p53, ER, PR, MLH1, PTEN, beta-catenin, p16, Ki-67, stathmin, ARID1A and L1CAM will be performed. Preoperative histology will be compared with the final pathology results. Follow-up will be at least 24 months to determine risk factors for recurrence and outcome. DISCUSSION: This study is designed to improve surgical treatment of endometrial carcinoma patients. A total of 432 endometrial carcinoma patients were enrolled between 2011 and 2013. Follow-up will be completed in 2015. Preoperative histology will be evaluated systematically and background endometrium will be classified. This is the first study incorporating immunohistochemistry, cervical cytology and comorbidity to define the optimal panel of prognostic biomarkers that contribute in clinical decision making in the management of endometrial carcinoma. TRIAL REGISTRATION: Netherlands Trial Register number NTR3503 BioMed Central 2015-06-30 /pmc/articles/PMC4485884/ /pubmed/26123742 http://dx.doi.org/10.1186/s12885-015-1487-3 Text en © Visser et al. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Visser, Nicole C. M.
Bulten, Johan
van der Wurff, Anneke A. M.
Boss, Erik A.
Bronkhorst, Carolien M.
Feijen, Harrie W. H.
Haartsen, Joke E.
van Herk, Hilde A. D. M.
de Kievit, Ineke M.
Klinkhamer, Paul J. J. M.
Pijlman, Brenda M.
Snijders, Marc P. M. L.
Vandenput, Ingrid
Vos, M. Caroline
de Wit, Peter E. J.
van de Poll-Franse, Lonneke V.
Massuger, Leon F.A.G.
Pijnenborg, Johanna M. A.
PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
title PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
title_full PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
title_fullStr PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
title_full_unstemmed PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
title_short PIpelle Prospective ENDOmetrial carcinoma (PIPENDO) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
title_sort pipelle prospective endometrial carcinoma (pipendo) study, pre-operative recognition of high risk endometrial carcinoma: a multicentre prospective cohort study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485884/
https://www.ncbi.nlm.nih.gov/pubmed/26123742
http://dx.doi.org/10.1186/s12885-015-1487-3
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