Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.

<h4>Objective</h4>Assess interpretative variation in Nottingham grading using control charts (CCs) and in silico kappa (ISK).<h4>Methods</h4>In house invasive breast cancer cases (2011-2019) at two institutions with a synoptic report were extracted. Pathologist interpretative...

Full description

Bibliographic Details
Main Authors: Jinesa Moodley, Phillip Williams, Gabriela Gohla, Pierre Major, Michael Bonert
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0242656
id doaj-719366f8622e471390ec01d8198d5680
record_format Article
spelling doaj-719366f8622e471390ec01d8198d56802021-03-04T12:48:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-011512e024265610.1371/journal.pone.0242656Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.Jinesa MoodleyPhillip WilliamsGabriela GohlaPierre MajorMichael Bonert<h4>Objective</h4>Assess interpretative variation in Nottingham grading using control charts (CCs) and in silico kappa (ISK).<h4>Methods</h4>In house invasive breast cancer cases (2011-2019) at two institutions with a synoptic report were extracted. Pathologist interpretative rates (PIRs) were calculated and normed for Nottingham grade (G) and its components (tubular score (TS), nuclear score (NS), mitotic score (MS)) for pathologists interpreting >35 cases. ISKs were calculated using the ordered mutually exclusive category assumption (OMECA) and maximal categorical overlap assumption (MCOA).<h4>Results</h4>The study period included 1,994 resections. Ten pathologists each assessed 38-441 cases and together saw 1,636; these were further analyzed. The PIR medians (normed ranges) were: G1:24%(18-27%), G2:53%(43-56%) and G3:26%(19-33%). The MCOA ISK and the number of statistical outliers (p< 0.05/p< 0.001) to the group median interpretive rate (GMIR) for the ten pathologists was G1: 0.82(2/0 of 10), G2: 0.76(1/1), G3: 0.71(3/1), TS1: 0.79(1/0), TS2: 0.63(5/1), TS3: 0.66(5/1), NS1: 0.37(5/4), NS2: 0.60(4/3), NS3: 0.59(4/4), MS1: 0.78(3/1), MS2: 0.78(3/1), MS3: 0.77(2/0). The OMECA ISK was 0.62, 0.49, 0.69 and 0.71 for TS, NS, MS and G.<h4>Conclusions</h4>The nuclear score has the most outliers. NS1 appears to be inconsistently used. ISK mirrors trends in conventional kappa studies. CCs and ISK allow insight into interpretive variation and may be essential for the next generation in quality.https://doi.org/10.1371/journal.pone.0242656
collection DOAJ
language English
format Article
sources DOAJ
author Jinesa Moodley
Phillip Williams
Gabriela Gohla
Pierre Major
Michael Bonert
spellingShingle Jinesa Moodley
Phillip Williams
Gabriela Gohla
Pierre Major
Michael Bonert
Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
PLoS ONE
author_facet Jinesa Moodley
Phillip Williams
Gabriela Gohla
Pierre Major
Michael Bonert
author_sort Jinesa Moodley
title Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
title_short Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
title_full Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
title_fullStr Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
title_full_unstemmed Variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
title_sort variation in breast cancer grading in 1,636 resections assessed using control charts and in silico kappa.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description <h4>Objective</h4>Assess interpretative variation in Nottingham grading using control charts (CCs) and in silico kappa (ISK).<h4>Methods</h4>In house invasive breast cancer cases (2011-2019) at two institutions with a synoptic report were extracted. Pathologist interpretative rates (PIRs) were calculated and normed for Nottingham grade (G) and its components (tubular score (TS), nuclear score (NS), mitotic score (MS)) for pathologists interpreting >35 cases. ISKs were calculated using the ordered mutually exclusive category assumption (OMECA) and maximal categorical overlap assumption (MCOA).<h4>Results</h4>The study period included 1,994 resections. Ten pathologists each assessed 38-441 cases and together saw 1,636; these were further analyzed. The PIR medians (normed ranges) were: G1:24%(18-27%), G2:53%(43-56%) and G3:26%(19-33%). The MCOA ISK and the number of statistical outliers (p< 0.05/p< 0.001) to the group median interpretive rate (GMIR) for the ten pathologists was G1: 0.82(2/0 of 10), G2: 0.76(1/1), G3: 0.71(3/1), TS1: 0.79(1/0), TS2: 0.63(5/1), TS3: 0.66(5/1), NS1: 0.37(5/4), NS2: 0.60(4/3), NS3: 0.59(4/4), MS1: 0.78(3/1), MS2: 0.78(3/1), MS3: 0.77(2/0). The OMECA ISK was 0.62, 0.49, 0.69 and 0.71 for TS, NS, MS and G.<h4>Conclusions</h4>The nuclear score has the most outliers. NS1 appears to be inconsistently used. ISK mirrors trends in conventional kappa studies. CCs and ISK allow insight into interpretive variation and may be essential for the next generation in quality.
url https://doi.org/10.1371/journal.pone.0242656
work_keys_str_mv AT jinesamoodley variationinbreastcancergradingin1636resectionsassessedusingcontrolchartsandinsilicokappa
AT phillipwilliams variationinbreastcancergradingin1636resectionsassessedusingcontrolchartsandinsilicokappa
AT gabrielagohla variationinbreastcancergradingin1636resectionsassessedusingcontrolchartsandinsilicokappa
AT pierremajor variationinbreastcancergradingin1636resectionsassessedusingcontrolchartsandinsilicokappa
AT michaelbonert variationinbreastcancergradingin1636resectionsassessedusingcontrolchartsandinsilicokappa
_version_ 1714801434450460672