Context.-Precise subtype diagnosis of non-small cell lung carcinoma is increasingly relevant, based on the availability of subtype-specific therapies, such as bevacizumab and pemetrexed, and based on the subtype-specific prevalence of activating epidermal growth factor receptor mutations. Objectives.-To establish a baseline measure of interobserver reproducibility for non-small cell lung carcinoma diagnoses with hematoxylin-eosin for the current 2004 World Health Organization classification, to estimate interobserver reproducibility for the therapeutically relevant squamous/nonsquamous subsets, and to examine characteristics that improve interobserver reproducibility. Design.-Primary, resected lung cancer specimens were converted to digital (virtual) slides. Based on a single hematoxylin-eosin virtual slide, pathologists were asked to assign a diagnosis using the 2004 World Health Organization classification. Kappa statistics were calculated for each pathologist-pair for each slide and were summarized by classification scheme, pulmonary pathology expertise, diagnostic confidence, and neoplastic grade. Results.-The 12 pulmonary pathology experts and the 12 community pathologists each independently diagnosed 48 to 96 single hematoxylin-eosin digital slides derived from 96 cases of non-small cell lung carcinoma resection. Overall agreement improved with simplification from the comprehensive 44 World Health Organization diagnoses (kappa = 0.25) to their 10 major header subtypes (kappa = 0.48) and improved again with simplification into the therapeutically relevant squamous/nonsquamous dichotomy (kappa = 0.55). Multivariate analysis showed that higher diagnostic agreement was associated with better differentiation, better slide quality, higher diagnostic confidence, similar years of pathology experience, and pulmonary pathology expertise. Conclusions.-These data define the baseline diagnostic agreement for hematoxylin-eosin diagnosis of non-small cell lung carcinoma, allowing future studies to test for improved diagnostic agreement with reflex ancillary tests. (Arch Pathol Lab Med. 2013;137:32-40; doi: 10.5858/arpa.2012-0033-OA)

Validation of Interobserver Agreement in Lung Cancer Assessment: Hematoxylin-Eosin Diagnostic Reproducibility for Non-Small Cell Lung Cancer The 2004 World Health Organization Classification and Therapeutically Relevant Subsets / Grilley-Olson, Je; Hayes, Dn; Moore, Dt; Leslie, Ko; Wilkerson, Md; Qaqish, Bf; Hayward, Mc; Cabanski, Cr; Yin, Xy; Socinski, Ma; Stinchcombe, Te; Thorne, Lb; Allen, Tc; Banks, Pm; Beasley, Mb; Borczuk, Ac; Cagle, Pt; Christensen, R; Colby, Tv; Deblois, Gg; Elmberger, G; Graziano, P; Hart, Cf; Jones, Kd; Maia, Dm; Miller, Cr; Nance, Kv; Travis, Wd; Funkhouser, Wk. - In: ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE. - ISSN 0003-9985. - 137:1(2013), pp. 32-40. [10.5858/arpa.2012-0033-OA]

Validation of Interobserver Agreement in Lung Cancer Assessment: Hematoxylin-Eosin Diagnostic Reproducibility for Non-Small Cell Lung Cancer The 2004 World Health Organization Classification and Therapeutically Relevant Subsets

Graziano P;
2013

Abstract

Context.-Precise subtype diagnosis of non-small cell lung carcinoma is increasingly relevant, based on the availability of subtype-specific therapies, such as bevacizumab and pemetrexed, and based on the subtype-specific prevalence of activating epidermal growth factor receptor mutations. Objectives.-To establish a baseline measure of interobserver reproducibility for non-small cell lung carcinoma diagnoses with hematoxylin-eosin for the current 2004 World Health Organization classification, to estimate interobserver reproducibility for the therapeutically relevant squamous/nonsquamous subsets, and to examine characteristics that improve interobserver reproducibility. Design.-Primary, resected lung cancer specimens were converted to digital (virtual) slides. Based on a single hematoxylin-eosin virtual slide, pathologists were asked to assign a diagnosis using the 2004 World Health Organization classification. Kappa statistics were calculated for each pathologist-pair for each slide and were summarized by classification scheme, pulmonary pathology expertise, diagnostic confidence, and neoplastic grade. Results.-The 12 pulmonary pathology experts and the 12 community pathologists each independently diagnosed 48 to 96 single hematoxylin-eosin digital slides derived from 96 cases of non-small cell lung carcinoma resection. Overall agreement improved with simplification from the comprehensive 44 World Health Organization diagnoses (kappa = 0.25) to their 10 major header subtypes (kappa = 0.48) and improved again with simplification into the therapeutically relevant squamous/nonsquamous dichotomy (kappa = 0.55). Multivariate analysis showed that higher diagnostic agreement was associated with better differentiation, better slide quality, higher diagnostic confidence, similar years of pathology experience, and pulmonary pathology expertise. Conclusions.-These data define the baseline diagnostic agreement for hematoxylin-eosin diagnosis of non-small cell lung carcinoma, allowing future studies to test for improved diagnostic agreement with reflex ancillary tests. (Arch Pathol Lab Med. 2013;137:32-40; doi: 10.5858/arpa.2012-0033-OA)
2013
Interobserver Agreement; lung cancer; classification
01 Pubblicazione su rivista::01a Articolo in rivista
Validation of Interobserver Agreement in Lung Cancer Assessment: Hematoxylin-Eosin Diagnostic Reproducibility for Non-Small Cell Lung Cancer The 2004 World Health Organization Classification and Therapeutically Relevant Subsets / Grilley-Olson, Je; Hayes, Dn; Moore, Dt; Leslie, Ko; Wilkerson, Md; Qaqish, Bf; Hayward, Mc; Cabanski, Cr; Yin, Xy; Socinski, Ma; Stinchcombe, Te; Thorne, Lb; Allen, Tc; Banks, Pm; Beasley, Mb; Borczuk, Ac; Cagle, Pt; Christensen, R; Colby, Tv; Deblois, Gg; Elmberger, G; Graziano, P; Hart, Cf; Jones, Kd; Maia, Dm; Miller, Cr; Nance, Kv; Travis, Wd; Funkhouser, Wk. - In: ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE. - ISSN 0003-9985. - 137:1(2013), pp. 32-40. [10.5858/arpa.2012-0033-OA]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1704591
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