TY - JOUR
T1 - Interobserver Variation among Pathologists and Refinement of Criteria in Distinguishing Separate Primary Tumors from Intrapulmonary Metastases in Lung
AU - Nicholson, Andrew G.
AU - Torkko, Kathleen
AU - Viola, Patrizia
AU - Duhig, Edwina
AU - Geisinger, Kim
AU - Borczuk, Alain C.
AU - Hiroshima, Kenzo
AU - Tsao, Ming S.
AU - Warth, Arne
AU - Lantuejoul, Sylvie
AU - Russell, Prudence A.
AU - Thunnissen, Erik
AU - Marchevsky, Alberto
AU - Mino-Kenudson, Mari
AU - Beasley, Mary Beth
AU - Botling, Johan
AU - Dacic, Sanja
AU - Yatabe, Yasushi
AU - Noguchi, Masayuki
AU - Travis, William D.
AU - Kerr, Keith
AU - Hirsch, Fred R.
AU - Chirieac, Lucian R.
AU - Wistuba, Ignacio I.
AU - Moreira, Andre
AU - Chung, Jin Haeng
AU - Chou, Teh Ying
AU - Bubendorf, Lukas
AU - Chen, Gang
AU - Pelosi, Giuseppe
AU - Poleri, Claudia
AU - Detterbeck, Frank C.
AU - Franklin, Wilbur A.
N1 - Publisher Copyright:
© 2017 International Association for the Study of Lung Cancer
PY - 2018/2
Y1 - 2018/2
N2 - Multiple tumor nodules are seen with increasing frequency in clinical practice. On the basis of the 2015 WHO classification of lung tumors, we assessed the reproducibility of the comprehensive histologic assessment to distinguish second primary lung cancers (SPLCs) from intrapulmonary metastases (IPMs), looking for the most distinctive histologic features. An international panel of lung pathologists reviewed a scanned sequential cohort of 126 tumors from 48 patients and recorded an agreed set of histologic features, including tumor typing and predominant pattern of adenocarcinoma, thereby opining whether the case was SPLC, IPM, or a combination thereof. Cohen κ statistics of 0.60 on overall assessment of SPLC or IPM indicated a good agreement. Likewise, there was good agreement (κ score 0.64, p < 0.0001) between WHO histologic pattern in individual cases and SPLC or IPM status, but the proportions diversified for histologic pattern and SPLC or IPM status (McNemar test, p < 0.0001). The strongest associations for distinguishing between SPLC and IPM were observed for nuclear pleomorphism, cell size, acinus formation, nucleolar size, mitotic rate, nuclear inclusions, intraalveolar clusters, and necrosis. Conversely, the associations for lymphocytosis, mucin content, lepidic growth, vascular invasion, macrophage response, clear cell change, acute inflammation keratinization, and emperipolesis did not reach significance with tumor extent. Comprehensive histologic assessment is recommended for distinguishing SPLC from IPM with good reproducibility among lung pathologists. In addition to main histologic type and predominant patterns of histologic subtypes, nuclear pleomorphism, cell size, acinus formation, nucleolar size, and mitotic rate strongly correlate with pathologic staging status.
AB - Multiple tumor nodules are seen with increasing frequency in clinical practice. On the basis of the 2015 WHO classification of lung tumors, we assessed the reproducibility of the comprehensive histologic assessment to distinguish second primary lung cancers (SPLCs) from intrapulmonary metastases (IPMs), looking for the most distinctive histologic features. An international panel of lung pathologists reviewed a scanned sequential cohort of 126 tumors from 48 patients and recorded an agreed set of histologic features, including tumor typing and predominant pattern of adenocarcinoma, thereby opining whether the case was SPLC, IPM, or a combination thereof. Cohen κ statistics of 0.60 on overall assessment of SPLC or IPM indicated a good agreement. Likewise, there was good agreement (κ score 0.64, p < 0.0001) between WHO histologic pattern in individual cases and SPLC or IPM status, but the proportions diversified for histologic pattern and SPLC or IPM status (McNemar test, p < 0.0001). The strongest associations for distinguishing between SPLC and IPM were observed for nuclear pleomorphism, cell size, acinus formation, nucleolar size, mitotic rate, nuclear inclusions, intraalveolar clusters, and necrosis. Conversely, the associations for lymphocytosis, mucin content, lepidic growth, vascular invasion, macrophage response, clear cell change, acute inflammation keratinization, and emperipolesis did not reach significance with tumor extent. Comprehensive histologic assessment is recommended for distinguishing SPLC from IPM with good reproducibility among lung pathologists. In addition to main histologic type and predominant patterns of histologic subtypes, nuclear pleomorphism, cell size, acinus formation, nucleolar size, and mitotic rate strongly correlate with pathologic staging status.
KW - Interobserver variation
KW - Lung cancer
KW - Multiple tumors
KW - Pathology
UR - http://www.scopus.com/inward/record.url?scp=85042443076&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85042443076&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2017.10.019
DO - 10.1016/j.jtho.2017.10.019
M3 - Article
C2 - 29127023
AN - SCOPUS:85042443076
SN - 1556-0864
VL - 13
SP - 205
EP - 217
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 2
ER -