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Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material

A shift toward a disease-based therapy designed according to patterns of failure and likelihood of nodal involvement predicted by pathologic determinants has recently led to considering a selective approach to lymphadenectomy for endometrial cancer. Therefore, it became critical to examine reproduci...

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Autores principales: Nofech-Mozes, S., Ismiil, N., Dubé, V., Saad, R. S., Ghorab, Z., Grin, A., Ackerman, I., Khalifa, M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306930/
https://www.ncbi.nlm.nih.gov/pubmed/22496699
http://dx.doi.org/10.1155/2012/414086
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author Nofech-Mozes, S.
Ismiil, N.
Dubé, V.
Saad, R. S.
Ghorab, Z.
Grin, A.
Ackerman, I.
Khalifa, M. A.
author_facet Nofech-Mozes, S.
Ismiil, N.
Dubé, V.
Saad, R. S.
Ghorab, Z.
Grin, A.
Ackerman, I.
Khalifa, M. A.
author_sort Nofech-Mozes, S.
collection PubMed
description A shift toward a disease-based therapy designed according to patterns of failure and likelihood of nodal involvement predicted by pathologic determinants has recently led to considering a selective approach to lymphadenectomy for endometrial cancer. Therefore, it became critical to examine reproducibility of diagnosing the key determinants of risk, on preoperative endometrial tissue samples as well as the concordance between preoperative and postresection specimens. Six gynaecologic pathologists assessed 105 consecutive endometrial biopsies originally reported as positive for endometrial cancer for cell type (endometrioid versus nonendometrioid), tumor grade (FIGO 3-tiered and 2-tiered), nuclear grade, and risk category (low risk defined as endometrioid histology, grade 1 + 2 and nuclear grade <3). Interrater agreement levels were substantial for identification of nonendometrioid histology (κ = 0.63; SE = 0.025), high tumor grade (κ = 0.64; SE = 0.025), and risk category (κ = 0.66; SE = 0.025). The overall agreement was fair for nuclear grade (κ = 0.21; SE = 0.025). There is agreement amongst pathologists in identifying high-risk pathologic determinants on endometrial cancer biopsies, and these highly correlate with postresection specimens. This is ascertainment prerequisite adaptation of the paradigm shift in surgical staging of patients with endometrial cancer.
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spelling pubmed-33069302012-04-11 Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material Nofech-Mozes, S. Ismiil, N. Dubé, V. Saad, R. S. Ghorab, Z. Grin, A. Ackerman, I. Khalifa, M. A. Obstet Gynecol Int Research Article A shift toward a disease-based therapy designed according to patterns of failure and likelihood of nodal involvement predicted by pathologic determinants has recently led to considering a selective approach to lymphadenectomy for endometrial cancer. Therefore, it became critical to examine reproducibility of diagnosing the key determinants of risk, on preoperative endometrial tissue samples as well as the concordance between preoperative and postresection specimens. Six gynaecologic pathologists assessed 105 consecutive endometrial biopsies originally reported as positive for endometrial cancer for cell type (endometrioid versus nonendometrioid), tumor grade (FIGO 3-tiered and 2-tiered), nuclear grade, and risk category (low risk defined as endometrioid histology, grade 1 + 2 and nuclear grade <3). Interrater agreement levels were substantial for identification of nonendometrioid histology (κ = 0.63; SE = 0.025), high tumor grade (κ = 0.64; SE = 0.025), and risk category (κ = 0.66; SE = 0.025). The overall agreement was fair for nuclear grade (κ = 0.21; SE = 0.025). There is agreement amongst pathologists in identifying high-risk pathologic determinants on endometrial cancer biopsies, and these highly correlate with postresection specimens. This is ascertainment prerequisite adaptation of the paradigm shift in surgical staging of patients with endometrial cancer. Hindawi Publishing Corporation 2012 2012-02-02 /pmc/articles/PMC3306930/ /pubmed/22496699 http://dx.doi.org/10.1155/2012/414086 Text en Copyright © 2012 S. Nofech-Mozes et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nofech-Mozes, S.
Ismiil, N.
Dubé, V.
Saad, R. S.
Ghorab, Z.
Grin, A.
Ackerman, I.
Khalifa, M. A.
Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material
title Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material
title_full Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material
title_fullStr Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material
title_full_unstemmed Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material
title_short Interobserver Agreement for Endometrial Cancer Characteristics Evaluated on Biopsy Material
title_sort interobserver agreement for endometrial cancer characteristics evaluated on biopsy material
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306930/
https://www.ncbi.nlm.nih.gov/pubmed/22496699
http://dx.doi.org/10.1155/2012/414086
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