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Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma

Low-grade and early Federation for Gynecology and Obstetrics (FIGO) stage endometrioid endometrial carcinomas (EEC) have an excellent prognosis. However, approximately 10% of patients develop recurrence, which cannot be correctly predicted at diagnosis. We evaluated myoinvasive patterns as a prognos...

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Autores principales: Ruz-Caracuel, Ignacio, Ramón-Patino, Jorge L, López-Janeiro, Álvaro, Yébenes, Laura, Berjón, Alberto, Hernández, Alicia, Gallego, Alejandro, Heredia-Soto, Victoria, Mendiola, Marta, Redondo, Andrés, Peláez-García, Alberto, Hardisson, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966575/
https://www.ncbi.nlm.nih.gov/pubmed/31766622
http://dx.doi.org/10.3390/cancers11121845
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author Ruz-Caracuel, Ignacio
Ramón-Patino, Jorge L
López-Janeiro, Álvaro
Yébenes, Laura
Berjón, Alberto
Hernández, Alicia
Gallego, Alejandro
Heredia-Soto, Victoria
Mendiola, Marta
Redondo, Andrés
Peláez-García, Alberto
Hardisson, David
author_facet Ruz-Caracuel, Ignacio
Ramón-Patino, Jorge L
López-Janeiro, Álvaro
Yébenes, Laura
Berjón, Alberto
Hernández, Alicia
Gallego, Alejandro
Heredia-Soto, Victoria
Mendiola, Marta
Redondo, Andrés
Peláez-García, Alberto
Hardisson, David
author_sort Ruz-Caracuel, Ignacio
collection PubMed
description Low-grade and early Federation for Gynecology and Obstetrics (FIGO) stage endometrioid endometrial carcinomas (EEC) have an excellent prognosis. However, approximately 10% of patients develop recurrence, which cannot be correctly predicted at diagnosis. We evaluated myoinvasive patterns as a prognostic factor of relapse in low-grade, early-stage EEC. Two-hundred and fifty-eight cases were selected according to the following inclusion criteria: (i) endometrioid endometrial carcinomas, (ii) grade 1 or 2 with (iii) FIGO stage I or II, and (iv) clinical follow-up. Slides were reviewed to annotate the myoinvasive pattern present in each case (infiltrative glands, microcystic, elongated and fragmented –MELF-, broad front, adenomyosis-like and adenoma malignum). Microsatellite instability was studied by immunoexpression of mismatch repair proteins (MLH1, PMS2, MSH2, and MSH6). There were 29 recurrences (11.2%) among the 258 cases analysed. A predominant broad front myoinvasive pattern was significantly associated with tumour relapse (p = 0.003). The presence of a pattern of infiltrative glands (p = 0.001) and microsatellite instability (p = 0.004) were associated with lower disease-free survival, without having an impact on overall survival. Our observations suggest the potential value of the pattern of myoinvasion as a prognostic factor in low-grade, early-stage endometrioid endometrial carcinoma.
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spelling pubmed-69665752020-01-27 Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma Ruz-Caracuel, Ignacio Ramón-Patino, Jorge L López-Janeiro, Álvaro Yébenes, Laura Berjón, Alberto Hernández, Alicia Gallego, Alejandro Heredia-Soto, Victoria Mendiola, Marta Redondo, Andrés Peláez-García, Alberto Hardisson, David Cancers (Basel) Article Low-grade and early Federation for Gynecology and Obstetrics (FIGO) stage endometrioid endometrial carcinomas (EEC) have an excellent prognosis. However, approximately 10% of patients develop recurrence, which cannot be correctly predicted at diagnosis. We evaluated myoinvasive patterns as a prognostic factor of relapse in low-grade, early-stage EEC. Two-hundred and fifty-eight cases were selected according to the following inclusion criteria: (i) endometrioid endometrial carcinomas, (ii) grade 1 or 2 with (iii) FIGO stage I or II, and (iv) clinical follow-up. Slides were reviewed to annotate the myoinvasive pattern present in each case (infiltrative glands, microcystic, elongated and fragmented –MELF-, broad front, adenomyosis-like and adenoma malignum). Microsatellite instability was studied by immunoexpression of mismatch repair proteins (MLH1, PMS2, MSH2, and MSH6). There were 29 recurrences (11.2%) among the 258 cases analysed. A predominant broad front myoinvasive pattern was significantly associated with tumour relapse (p = 0.003). The presence of a pattern of infiltrative glands (p = 0.001) and microsatellite instability (p = 0.004) were associated with lower disease-free survival, without having an impact on overall survival. Our observations suggest the potential value of the pattern of myoinvasion as a prognostic factor in low-grade, early-stage endometrioid endometrial carcinoma. MDPI 2019-11-22 /pmc/articles/PMC6966575/ /pubmed/31766622 http://dx.doi.org/10.3390/cancers11121845 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ruz-Caracuel, Ignacio
Ramón-Patino, Jorge L
López-Janeiro, Álvaro
Yébenes, Laura
Berjón, Alberto
Hernández, Alicia
Gallego, Alejandro
Heredia-Soto, Victoria
Mendiola, Marta
Redondo, Andrés
Peláez-García, Alberto
Hardisson, David
Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma
title Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma
title_full Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma
title_fullStr Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma
title_full_unstemmed Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma
title_short Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma
title_sort myoinvasive pattern as a prognostic marker in low-grade, early-stage endometrioid endometrial carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966575/
https://www.ncbi.nlm.nih.gov/pubmed/31766622
http://dx.doi.org/10.3390/cancers11121845
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