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Details of human epidermal growth factor receptor 2 status in 454 cases of biliary tract cancer
Human epidermal growth factor receptor 2 (HER2)-targeted therapy has improved clinical outcomes in patients with HER2-positive breast and gastric cancers, although ineffective or recurrent cases are present. One reason for this is the heterogeneity of HER2 expression in cancer cells. The aim of this...
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Published in: | Human pathology 2020-11, Vol.105, p.9-19 |
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description | Human epidermal growth factor receptor 2 (HER2)-targeted therapy has improved clinical outcomes in patients with HER2-positive breast and gastric cancers, although ineffective or recurrent cases are present. One reason for this is the heterogeneity of HER2 expression in cancer cells. The aim of this study was to investigate the clinicopathological characteristics and HER2 status of patients with biliary tract cancers (BTCs). We examined HER2 protein expression by immunohistochemistry, HER2 gene amplification by fluorescence in situ hybridization, and both HER2 protein and gene levels simultaneously by gene-protein assay. Samples were collected from 454 patients who underwent surgical resection for BTCs (110 intrahepatic cholangiocarcinomas [ICC], 67 perihilar extrahepatic cholangiocarcinomas [ECC-Bp], 119 distal extrahepatic cholangiocarcinomas [ECC-Bd], 80 gallbladder carcinomas [GBC], and 79 ampullary carcinomas [AVC]). HER2 status was assessed according to the guidelines for HER2 testing in gastroesophageal adenocarcinoma. HER2-positive status was detected in 14.5% of BTCs (3.7% of ICC, 3.0% of ECC-Bp, 18.5% of ECC-Bd, 31.3% of GBC, and 16.4% of AVC). Furthermore, HER2-positivity tended to correlate with low histological grade, tumor histology, and macroscopic features in certain tumors. HER2 heterogeneity was common and highly frequent (83%) in BTC cases. Reduced HER2 protein expression in the deeper invasive areas with simultaneous dedifferentiation was frequently observed in HER2-positive cancer cells. The findings of this study suggest that a large subgroup of HER2-positive BTC cases can be considered for HER2-targeted therapy. Moreover, the HER2 status in BTCs should be determined carefully using a sensitive approach toward larger cancer tissues.
•The frequency of human epidermal growth factor receptor 2 (HER2) positivity differed among various biliary tract cancers (BTCs).•HER2 heterogeneity was commonly and frequently (83%) observed among BTCs.•HER2 heterogeneity was not associated with patient outcome.•Even though nearly all patients with a homogenous HER2-positive status survived. |
doi_str_mv | 10.1016/j.humpath.2020.08.006 |
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•The frequency of human epidermal growth factor receptor 2 (HER2) positivity differed among various biliary tract cancers (BTCs).•HER2 heterogeneity was commonly and frequently (83%) observed among BTCs.•HER2 heterogeneity was not associated with patient outcome.•Even though nearly all patients with a homogenous HER2-positive status survived.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2020.08.006</identifier><identifier>PMID: 32891647</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Biliary tract cancer ; Biliary Tract Neoplasms - enzymology ; Biliary Tract Neoplasms - genetics ; Biliary Tract Neoplasms - pathology ; Biliary Tract Neoplasms - surgery ; Biomarkers, Tumor - analysis ; Biomarkers, Tumor - genetics ; Cancer therapies ; Cholangiocarcinoma ; Epidermal growth factor ; Female ; Gallbladder ; Gene Amplification ; Genetic Predisposition to Disease ; HER2 ; Heterogeneity ; Humans ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Kinases ; Male ; Medical prognosis ; Papillary adenocarcinoma ; Patients ; Phenotype ; Proteins ; Receptor, ErbB-2 - analysis ; Receptor, ErbB-2 - genetics ; Targeted therapy ; Tumors</subject><ispartof>Human pathology, 2020-11, Vol.105, p.9-19</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><rights>2020. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-463f04b04e95f899765c8e915905e98366ee8ee29e0a6021857e089e2107ad483</citedby><cites>FETCH-LOGICAL-c393t-463f04b04e95f899765c8e915905e98366ee8ee29e0a6021857e089e2107ad483</cites><orcidid>0000-0003-4215-4385 ; 0000-0002-7569-7813 ; 0000-0002-9153-3798 ; 0000-0002-3516-8765</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32891647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hiraoka, Nobuyoshi</creatorcontrib><creatorcontrib>Nitta, Hiroaki</creatorcontrib><creatorcontrib>Ohba, Akihiro</creatorcontrib><creatorcontrib>Yoshida, Hiroshi</creatorcontrib><creatorcontrib>Morizane, Chigusa</creatorcontrib><creatorcontrib>Okusaka, Takuji</creatorcontrib><creatorcontrib>Nara, Satoshi</creatorcontrib><creatorcontrib>Esaki, Minoru</creatorcontrib><creatorcontrib>Kishi, Yoji</creatorcontrib><creatorcontrib>Shimada, Kazuaki</creatorcontrib><title>Details of human epidermal growth factor receptor 2 status in 454 cases of biliary tract cancer</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Human epidermal growth factor receptor 2 (HER2)-targeted therapy has improved clinical outcomes in patients with HER2-positive breast and gastric cancers, although ineffective or recurrent cases are present. One reason for this is the heterogeneity of HER2 expression in cancer cells. The aim of this study was to investigate the clinicopathological characteristics and HER2 status of patients with biliary tract cancers (BTCs). We examined HER2 protein expression by immunohistochemistry, HER2 gene amplification by fluorescence in situ hybridization, and both HER2 protein and gene levels simultaneously by gene-protein assay. Samples were collected from 454 patients who underwent surgical resection for BTCs (110 intrahepatic cholangiocarcinomas [ICC], 67 perihilar extrahepatic cholangiocarcinomas [ECC-Bp], 119 distal extrahepatic cholangiocarcinomas [ECC-Bd], 80 gallbladder carcinomas [GBC], and 79 ampullary carcinomas [AVC]). HER2 status was assessed according to the guidelines for HER2 testing in gastroesophageal adenocarcinoma. HER2-positive status was detected in 14.5% of BTCs (3.7% of ICC, 3.0% of ECC-Bp, 18.5% of ECC-Bd, 31.3% of GBC, and 16.4% of AVC). Furthermore, HER2-positivity tended to correlate with low histological grade, tumor histology, and macroscopic features in certain tumors. HER2 heterogeneity was common and highly frequent (83%) in BTC cases. Reduced HER2 protein expression in the deeper invasive areas with simultaneous dedifferentiation was frequently observed in HER2-positive cancer cells. The findings of this study suggest that a large subgroup of HER2-positive BTC cases can be considered for HER2-targeted therapy. Moreover, the HER2 status in BTCs should be determined carefully using a sensitive approach toward larger cancer tissues.
•The frequency of human epidermal growth factor receptor 2 (HER2) positivity differed among various biliary tract cancers (BTCs).•HER2 heterogeneity was commonly and frequently (83%) observed among BTCs.•HER2 heterogeneity was not associated with patient outcome.•Even though nearly all patients with a homogenous HER2-positive status survived.</description><subject>Aged</subject><subject>Biliary tract cancer</subject><subject>Biliary Tract Neoplasms - enzymology</subject><subject>Biliary Tract Neoplasms - genetics</subject><subject>Biliary Tract Neoplasms - pathology</subject><subject>Biliary Tract Neoplasms - surgery</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Cancer therapies</subject><subject>Cholangiocarcinoma</subject><subject>Epidermal growth factor</subject><subject>Female</subject><subject>Gallbladder</subject><subject>Gene Amplification</subject><subject>Genetic Predisposition to Disease</subject><subject>HER2</subject><subject>Heterogeneity</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Kinases</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Papillary adenocarcinoma</subject><subject>Patients</subject><subject>Phenotype</subject><subject>Proteins</subject><subject>Receptor, ErbB-2 - analysis</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>Targeted therapy</subject><subject>Tumors</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EgvL4BJAl1gljx3bsFUK8JSQ2sLbcZEJdtU2wHRB_j0sLW1YzGt17Z-YQcsqgZMDUxbycjcvBpVnJgUMJugRQO2TCZMULXRm-SyYAQhWa1fUBOYxxDsCYFHKfHFRcG6ZEPSH2BpPzi0j7juZAt6I4-BbD0i3oW-g_04x2rkl9oAEbHNYNpzG5NEbqV1RIQRsX8cc_9QvvwhdNITvyeNVgOCZ7nVtEPNnWI_J6d_ty_VA8Pd8_Xl89FU1lqlQIVXUgpiDQyE4bUyvZaDRMGpBodKUUokbkBsEp4EzLGkEb5Axq1wpdHZHzTe4Q-vcRY7LzfgyrvNJyoTgAl8pkldyomtDHGLCzQ_DLfLNlYNdY7dxusdo1VgvaZqzZd7ZNH6dLbP9cvxyz4HIjwPzjh8dgY-MxA2h95pZs2_t_VnwDNIKJ9A</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Hiraoka, Nobuyoshi</creator><creator>Nitta, Hiroaki</creator><creator>Ohba, Akihiro</creator><creator>Yoshida, Hiroshi</creator><creator>Morizane, Chigusa</creator><creator>Okusaka, Takuji</creator><creator>Nara, Satoshi</creator><creator>Esaki, Minoru</creator><creator>Kishi, Yoji</creator><creator>Shimada, Kazuaki</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0003-4215-4385</orcidid><orcidid>https://orcid.org/0000-0002-7569-7813</orcidid><orcidid>https://orcid.org/0000-0002-9153-3798</orcidid><orcidid>https://orcid.org/0000-0002-3516-8765</orcidid></search><sort><creationdate>202011</creationdate><title>Details of human epidermal growth factor receptor 2 status in 454 cases of biliary tract cancer</title><author>Hiraoka, Nobuyoshi ; Nitta, Hiroaki ; Ohba, Akihiro ; Yoshida, Hiroshi ; Morizane, Chigusa ; Okusaka, Takuji ; Nara, Satoshi ; Esaki, Minoru ; Kishi, Yoji ; Shimada, Kazuaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-463f04b04e95f899765c8e915905e98366ee8ee29e0a6021857e089e2107ad483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Biliary tract cancer</topic><topic>Biliary Tract Neoplasms - enzymology</topic><topic>Biliary Tract Neoplasms - genetics</topic><topic>Biliary Tract Neoplasms - pathology</topic><topic>Biliary Tract Neoplasms - surgery</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Cancer therapies</topic><topic>Cholangiocarcinoma</topic><topic>Epidermal growth factor</topic><topic>Female</topic><topic>Gallbladder</topic><topic>Gene Amplification</topic><topic>Genetic Predisposition to Disease</topic><topic>HER2</topic><topic>Heterogeneity</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Kinases</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Papillary adenocarcinoma</topic><topic>Patients</topic><topic>Phenotype</topic><topic>Proteins</topic><topic>Receptor, ErbB-2 - analysis</topic><topic>Receptor, ErbB-2 - genetics</topic><topic>Targeted therapy</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hiraoka, Nobuyoshi</creatorcontrib><creatorcontrib>Nitta, Hiroaki</creatorcontrib><creatorcontrib>Ohba, Akihiro</creatorcontrib><creatorcontrib>Yoshida, Hiroshi</creatorcontrib><creatorcontrib>Morizane, Chigusa</creatorcontrib><creatorcontrib>Okusaka, Takuji</creatorcontrib><creatorcontrib>Nara, Satoshi</creatorcontrib><creatorcontrib>Esaki, Minoru</creatorcontrib><creatorcontrib>Kishi, Yoji</creatorcontrib><creatorcontrib>Shimada, Kazuaki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hiraoka, Nobuyoshi</au><au>Nitta, Hiroaki</au><au>Ohba, Akihiro</au><au>Yoshida, Hiroshi</au><au>Morizane, Chigusa</au><au>Okusaka, Takuji</au><au>Nara, Satoshi</au><au>Esaki, Minoru</au><au>Kishi, Yoji</au><au>Shimada, Kazuaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Details of human epidermal growth factor receptor 2 status in 454 cases of biliary tract cancer</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2020-11</date><risdate>2020</risdate><volume>105</volume><spage>9</spage><epage>19</epage><pages>9-19</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Human epidermal growth factor receptor 2 (HER2)-targeted therapy has improved clinical outcomes in patients with HER2-positive breast and gastric cancers, although ineffective or recurrent cases are present. One reason for this is the heterogeneity of HER2 expression in cancer cells. The aim of this study was to investigate the clinicopathological characteristics and HER2 status of patients with biliary tract cancers (BTCs). We examined HER2 protein expression by immunohistochemistry, HER2 gene amplification by fluorescence in situ hybridization, and both HER2 protein and gene levels simultaneously by gene-protein assay. Samples were collected from 454 patients who underwent surgical resection for BTCs (110 intrahepatic cholangiocarcinomas [ICC], 67 perihilar extrahepatic cholangiocarcinomas [ECC-Bp], 119 distal extrahepatic cholangiocarcinomas [ECC-Bd], 80 gallbladder carcinomas [GBC], and 79 ampullary carcinomas [AVC]). HER2 status was assessed according to the guidelines for HER2 testing in gastroesophageal adenocarcinoma. HER2-positive status was detected in 14.5% of BTCs (3.7% of ICC, 3.0% of ECC-Bp, 18.5% of ECC-Bd, 31.3% of GBC, and 16.4% of AVC). Furthermore, HER2-positivity tended to correlate with low histological grade, tumor histology, and macroscopic features in certain tumors. HER2 heterogeneity was common and highly frequent (83%) in BTC cases. Reduced HER2 protein expression in the deeper invasive areas with simultaneous dedifferentiation was frequently observed in HER2-positive cancer cells. The findings of this study suggest that a large subgroup of HER2-positive BTC cases can be considered for HER2-targeted therapy. Moreover, the HER2 status in BTCs should be determined carefully using a sensitive approach toward larger cancer tissues.
•The frequency of human epidermal growth factor receptor 2 (HER2) positivity differed among various biliary tract cancers (BTCs).•HER2 heterogeneity was commonly and frequently (83%) observed among BTCs.•HER2 heterogeneity was not associated with patient outcome.•Even though nearly all patients with a homogenous HER2-positive status survived.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32891647</pmid><doi>10.1016/j.humpath.2020.08.006</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4215-4385</orcidid><orcidid>https://orcid.org/0000-0002-7569-7813</orcidid><orcidid>https://orcid.org/0000-0002-9153-3798</orcidid><orcidid>https://orcid.org/0000-0002-3516-8765</orcidid></addata></record> |
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subjects | Aged Biliary tract cancer Biliary Tract Neoplasms - enzymology Biliary Tract Neoplasms - genetics Biliary Tract Neoplasms - pathology Biliary Tract Neoplasms - surgery Biomarkers, Tumor - analysis Biomarkers, Tumor - genetics Cancer therapies Cholangiocarcinoma Epidermal growth factor Female Gallbladder Gene Amplification Genetic Predisposition to Disease HER2 Heterogeneity Humans Immunohistochemistry In Situ Hybridization, Fluorescence Kinases Male Medical prognosis Papillary adenocarcinoma Patients Phenotype Proteins Receptor, ErbB-2 - analysis Receptor, ErbB-2 - genetics Targeted therapy Tumors |
title | Details of human epidermal growth factor receptor 2 status in 454 cases of biliary tract cancer |
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