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Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer
Clinical significance of the pT4 category in colon cancer is increasing with several therapeutic implications. The aim of this study was to evaluate variability in diagnosing pT4a colon cancer. Twelve pathologists classified 66 preselected scanned Hematoxylin/Eosin-stained slides with tumor cells at...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028812/ https://www.ncbi.nlm.nih.gov/pubmed/31616981 http://dx.doi.org/10.1007/s00428-019-02663-0 |
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author | Klaver, Charlotte E. L. Bulkmans, Nicole Drillenburg, Paul Grabsch, Heike I. van Grieken, Nicole C. T. Karrenbeld, Arend Koens, Lianne van Lijnschoten, Ineke Meijer, Jos Nagtegaal, Iris D. Sagaert, Xavier Seldenrijk, Kees van Velthuysen, M. F. Bruggink, Annette H. Tanis, Pieter J. Snaebjornsson, Petur |
author_facet | Klaver, Charlotte E. L. Bulkmans, Nicole Drillenburg, Paul Grabsch, Heike I. van Grieken, Nicole C. T. Karrenbeld, Arend Koens, Lianne van Lijnschoten, Ineke Meijer, Jos Nagtegaal, Iris D. Sagaert, Xavier Seldenrijk, Kees van Velthuysen, M. F. Bruggink, Annette H. Tanis, Pieter J. Snaebjornsson, Petur |
author_sort | Klaver, Charlotte E. L. |
collection | PubMed |
description | Clinical significance of the pT4 category in colon cancer is increasing with several therapeutic implications. The aim of this study was to evaluate variability in diagnosing pT4a colon cancer. Twelve pathologists classified 66 preselected scanned Hematoxylin/Eosin-stained slides with tumor cells at a distance of 25–1500 μm (n = 22), 0–25 μm (n = 22), or on (n = 22) the peritoneal surface. Inter- and intraobserver variability were calculated using Kappa statistics. For interlaboratory variability, pathology reports of pT3 and pT4a colon cancer were extracted from the Dutch Pathology Registry between 2012 and 2015. The proportion of pT4a (pT4a/(pT3+pT4a)) was compared between 33 laboratories. Potential risk of understaging was assessed by determining the average number of blocks taken from pT3 and pT4a N0-2M0 tumors with metachronous peritoneal metastasis. Interobserver variability among 12 pathologists was 0.50 (95%CI 0.41–0.60; moderate agreement). Intraobserver variability (8 pathologists) was 0.71 (substantial agreement). A total of 7745 reports with pT3 or pT4aN0-2M0 colon cancer from 33 laboratories were included for interlaboratory analysis. Median percentage of pT4a was 15.5% (range 3.2–24.6%). After adjustment for case mix, 8 labs diagnosed pT4a significantly less or more frequently than the median lab. Metachronous peritoneal metastases were histologically verified in 170 of 6629 pT3 and in 129 of 1116 pT4a tumors, with a mean number of blocks of 4.03(SD 1.51) and 4.78 (SD 1.76) taken from the primary tumors, respectively (p < 0.001). A substantial variability in diagnosing pT4a colon cancer exists, both at pathologist and laboratory level. Diagnosis of pT4a stage appears to be challenging and there is a need for standardizing assessment of this pathological entity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00428-019-02663-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7028812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70288122020-03-02 Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer Klaver, Charlotte E. L. Bulkmans, Nicole Drillenburg, Paul Grabsch, Heike I. van Grieken, Nicole C. T. Karrenbeld, Arend Koens, Lianne van Lijnschoten, Ineke Meijer, Jos Nagtegaal, Iris D. Sagaert, Xavier Seldenrijk, Kees van Velthuysen, M. F. Bruggink, Annette H. Tanis, Pieter J. Snaebjornsson, Petur Virchows Arch Original Article Clinical significance of the pT4 category in colon cancer is increasing with several therapeutic implications. The aim of this study was to evaluate variability in diagnosing pT4a colon cancer. Twelve pathologists classified 66 preselected scanned Hematoxylin/Eosin-stained slides with tumor cells at a distance of 25–1500 μm (n = 22), 0–25 μm (n = 22), or on (n = 22) the peritoneal surface. Inter- and intraobserver variability were calculated using Kappa statistics. For interlaboratory variability, pathology reports of pT3 and pT4a colon cancer were extracted from the Dutch Pathology Registry between 2012 and 2015. The proportion of pT4a (pT4a/(pT3+pT4a)) was compared between 33 laboratories. Potential risk of understaging was assessed by determining the average number of blocks taken from pT3 and pT4a N0-2M0 tumors with metachronous peritoneal metastasis. Interobserver variability among 12 pathologists was 0.50 (95%CI 0.41–0.60; moderate agreement). Intraobserver variability (8 pathologists) was 0.71 (substantial agreement). A total of 7745 reports with pT3 or pT4aN0-2M0 colon cancer from 33 laboratories were included for interlaboratory analysis. Median percentage of pT4a was 15.5% (range 3.2–24.6%). After adjustment for case mix, 8 labs diagnosed pT4a significantly less or more frequently than the median lab. Metachronous peritoneal metastases were histologically verified in 170 of 6629 pT3 and in 129 of 1116 pT4a tumors, with a mean number of blocks of 4.03(SD 1.51) and 4.78 (SD 1.76) taken from the primary tumors, respectively (p < 0.001). A substantial variability in diagnosing pT4a colon cancer exists, both at pathologist and laboratory level. Diagnosis of pT4a stage appears to be challenging and there is a need for standardizing assessment of this pathological entity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00428-019-02663-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-10-16 2020 /pmc/articles/PMC7028812/ /pubmed/31616981 http://dx.doi.org/10.1007/s00428-019-02663-0 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Klaver, Charlotte E. L. Bulkmans, Nicole Drillenburg, Paul Grabsch, Heike I. van Grieken, Nicole C. T. Karrenbeld, Arend Koens, Lianne van Lijnschoten, Ineke Meijer, Jos Nagtegaal, Iris D. Sagaert, Xavier Seldenrijk, Kees van Velthuysen, M. F. Bruggink, Annette H. Tanis, Pieter J. Snaebjornsson, Petur Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer |
title | Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer |
title_full | Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer |
title_fullStr | Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer |
title_full_unstemmed | Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer |
title_short | Interobserver, intraobserver, and interlaboratory variability in reporting pT4a colon cancer |
title_sort | interobserver, intraobserver, and interlaboratory variability in reporting pt4a colon cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028812/ https://www.ncbi.nlm.nih.gov/pubmed/31616981 http://dx.doi.org/10.1007/s00428-019-02663-0 |
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