HER2/HER3 pathway in biliary tract malignancies; systematic review and meta-analysis: a potential therapeutic target?
Human epidermal growth factor receptor 2 (HER2) overexpression and amplification have been reported as predictive markers for HER2-targeted therapy in breast and gastric cancer, whereas human epidermal growth factor receptor 3 (HER3) is emerging as a potential resistance factor. The aim of this stud...
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description | Human epidermal growth factor receptor 2 (HER2) overexpression and amplification have been reported as predictive markers for HER2-targeted therapy in breast and gastric cancer, whereas human epidermal growth factor receptor 3 (HER3) is emerging as a potential resistance factor. The aim of this study was to perform a systematic review and meta-analysis of the HER2 and HER3 overexpression and amplification in biliary tract cancers (BTCs). An electronic search of MEDLINE, American Society of Clinical Oncology (ASCO), European Society of Medical Oncology Congress (ESMO), and American Association for Cancer Research (AACR) was performed to identify studies reporting HER2 and/or HER3 membrane protein expression by immunohistochemistry (IHC) and/or gene amplification by
in situ
hybridization (ISH) in BTCs. Studies were classified as “high quality” (HQ) if IHC overexpression was defined as presence of moderate/strong staining or “low quality” (LQ) where “any” expression was considered positive. Of 440 studies screened, 40 met the inclusion criteria. Globally, HER2 expression rate was 26.5 % (95 % CI 18.9–34.1 %). When HQ studies were analyzed (
n
= 27 studies), extrahepatic BTCs showed a higher HER2 overexpression rate compared to intrahepatic cholangiocarcinoma: 19.9 % (95 % CI 12.8–27.1 %) vs. 4.8 % (95 % CI 0–14.5 %), respectively,
p
value 0.0049. HER2 amplification rate was higher in patients selected by HER2 overexpression compared to “unselected” patients: 57.6 % (95 % CI 16.2–99 %) vs. 17.9 % (95 % CI 0.1–35.4 %), respectively,
p
value 0.0072. HER3 overexpression (4/4 HQ studies) and amplification rates were 27.9 % (95 % CI 9.7–46.1 %) and 26.5 % (one study), respectively. Up to 20 % of extrahepatic BTCs appear to be HER2 overexpressed; of these, close to 60 % appear to be HER2 amplified, while HER3 is overexpressed or amplified in about 25 % of patients. Clinical relevance for targeted therapy should be tested in prospective clinical trials. |
doi_str_mv | 10.1007/s10555-016-9645-x |
format | Article |
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in situ
hybridization (ISH) in BTCs. Studies were classified as “high quality” (HQ) if IHC overexpression was defined as presence of moderate/strong staining or “low quality” (LQ) where “any” expression was considered positive. Of 440 studies screened, 40 met the inclusion criteria. Globally, HER2 expression rate was 26.5 % (95 % CI 18.9–34.1 %). When HQ studies were analyzed (
n
= 27 studies), extrahepatic BTCs showed a higher HER2 overexpression rate compared to intrahepatic cholangiocarcinoma: 19.9 % (95 % CI 12.8–27.1 %) vs. 4.8 % (95 % CI 0–14.5 %), respectively,
p
value 0.0049. HER2 amplification rate was higher in patients selected by HER2 overexpression compared to “unselected” patients: 57.6 % (95 % CI 16.2–99 %) vs. 17.9 % (95 % CI 0.1–35.4 %), respectively,
p
value 0.0072. HER3 overexpression (4/4 HQ studies) and amplification rates were 27.9 % (95 % CI 9.7–46.1 %) and 26.5 % (one study), respectively. Up to 20 % of extrahepatic BTCs appear to be HER2 overexpressed; of these, close to 60 % appear to be HER2 amplified, while HER3 is overexpressed or amplified in about 25 % of patients. Clinical relevance for targeted therapy should be tested in prospective clinical trials.</description><identifier>ISSN: 0167-7659</identifier><identifier>EISSN: 1573-7233</identifier><identifier>DOI: 10.1007/s10555-016-9645-x</identifier><identifier>PMID: 27981460</identifier><identifier>CODEN: CMRED4</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Analysis ; Biliary Tract Neoplasms - enzymology ; Biomedical and Life Sciences ; Biomedicine ; Cancer ; Cancer Research ; Database searching ; Epidermal growth factor ; Genetic research ; Health aspects ; Humans ; Immunohistochemistry ; Internet/Web search services ; Metabolic Networks and Pathways ; Non-Thematic Review ; Oncology ; Oncology, Experimental ; Online searching ; Receptor, ErbB-2 - biosynthesis ; Receptor, ErbB-2 - genetics ; Receptor, ErbB-2 - metabolism ; Receptor, ErbB-3 - biosynthesis ; Receptor, ErbB-3 - genetics ; Receptor, ErbB-3 - metabolism ; Stomach cancer</subject><ispartof>Cancer and metastasis reviews, 2017-03, Vol.36 (1), p.141-157</ispartof><rights>The Author(s) 2016</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Cancer and Metastasis Reviews is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c663t-de264dca7f65989ec7f7a0d4e97e84bd18b32e3170d046dec5bbb13ce6776ab3</citedby><cites>FETCH-LOGICAL-c663t-de264dca7f65989ec7f7a0d4e97e84bd18b32e3170d046dec5bbb13ce6776ab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10555-016-9645-x$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10555-016-9645-x$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27981460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Galdy, Salvatore</creatorcontrib><creatorcontrib>Lamarca, Angela</creatorcontrib><creatorcontrib>McNamara, Mairéad G.</creatorcontrib><creatorcontrib>Hubner, Richard A.</creatorcontrib><creatorcontrib>Cella, Chiara A.</creatorcontrib><creatorcontrib>Fazio, Nicola</creatorcontrib><creatorcontrib>Valle, Juan W.</creatorcontrib><title>HER2/HER3 pathway in biliary tract malignancies; systematic review and meta-analysis: a potential therapeutic target?</title><title>Cancer and metastasis reviews</title><addtitle>Cancer Metastasis Rev</addtitle><addtitle>Cancer Metastasis Rev</addtitle><description>Human epidermal growth factor receptor 2 (HER2) overexpression and amplification have been reported as predictive markers for HER2-targeted therapy in breast and gastric cancer, whereas human epidermal growth factor receptor 3 (HER3) is emerging as a potential resistance factor. The aim of this study was to perform a systematic review and meta-analysis of the HER2 and HER3 overexpression and amplification in biliary tract cancers (BTCs). An electronic search of MEDLINE, American Society of Clinical Oncology (ASCO), European Society of Medical Oncology Congress (ESMO), and American Association for Cancer Research (AACR) was performed to identify studies reporting HER2 and/or HER3 membrane protein expression by immunohistochemistry (IHC) and/or gene amplification by
in situ
hybridization (ISH) in BTCs. Studies were classified as “high quality” (HQ) if IHC overexpression was defined as presence of moderate/strong staining or “low quality” (LQ) where “any” expression was considered positive. Of 440 studies screened, 40 met the inclusion criteria. Globally, HER2 expression rate was 26.5 % (95 % CI 18.9–34.1 %). When HQ studies were analyzed (
n
= 27 studies), extrahepatic BTCs showed a higher HER2 overexpression rate compared to intrahepatic cholangiocarcinoma: 19.9 % (95 % CI 12.8–27.1 %) vs. 4.8 % (95 % CI 0–14.5 %), respectively,
p
value 0.0049. HER2 amplification rate was higher in patients selected by HER2 overexpression compared to “unselected” patients: 57.6 % (95 % CI 16.2–99 %) vs. 17.9 % (95 % CI 0.1–35.4 %), respectively,
p
value 0.0072. HER3 overexpression (4/4 HQ studies) and amplification rates were 27.9 % (95 % CI 9.7–46.1 %) and 26.5 % (one study), respectively. Up to 20 % of extrahepatic BTCs appear to be HER2 overexpressed; of these, close to 60 % appear to be HER2 amplified, while HER3 is overexpressed or amplified in about 25 % of patients. Clinical relevance for targeted therapy should be tested in prospective clinical trials.</description><subject>Analysis</subject><subject>Biliary Tract Neoplasms - enzymology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Database searching</subject><subject>Epidermal growth factor</subject><subject>Genetic research</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Internet/Web search services</subject><subject>Metabolic Networks and Pathways</subject><subject>Non-Thematic Review</subject><subject>Oncology</subject><subject>Oncology, Experimental</subject><subject>Online searching</subject><subject>Receptor, ErbB-2 - biosynthesis</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Receptor, ErbB-3 - biosynthesis</subject><subject>Receptor, ErbB-3 - genetics</subject><subject>Receptor, ErbB-3 - metabolism</subject><subject>Stomach cancer</subject><issn>0167-7659</issn><issn>1573-7233</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNktFr1TAUxosobk7_AF8k6Isv3ZKmSVoHyhjTCQNB9h5O09N7M9q0S9Jt97835c55JxMkkEDO7_vIOfmy7C2jh4xSdRQYFULklMm8lqXI755l-0wonquC8-fZfiqoXElR72WvQriiScNV_TLbK1RdsVLS_Ww-P_tZHKWNkwni-hY2xDrS2N6C35DowUQyQG9XDpyxGI5J2ISIA0RriMcbi7cEXEsGjJCDg34TbPhEgExjRBct9CSu0cOE86KI4FcYv7zOXnTQB3xzfx5kl1_PLk_P84sf376fnlzkRkoe8xYLWbYGVJd6qGo0qlNA2xJrhVXZtKxqeIGcKdrSUrZoRNM0jBuUSklo-EH2eWs7zc2ArUkP8tDrydshdadHsPpxxdm1Xo03WvBKsFolg4_3Bn68njFEPdhgsO_B4TgHzaqaVVXBy_o_UFHIKv3Sgn74C70aZ59mt1CVKFlRCvqHWkGP2rpuXH5jMdUnihW1FFJUiXr_BGUme613ocMnoLRaHKwZHXY23T9yZVuB8WMIHruHmTGql-jpbfR0Spheoqfvkubd7rAfFL-zloBiC4RUciv0O23_0_UXFiHj_w</recordid><startdate>20170301</startdate><enddate>20170301</enddate><creator>Galdy, Salvatore</creator><creator>Lamarca, Angela</creator><creator>McNamara, Mairéad G.</creator><creator>Hubner, Richard A.</creator><creator>Cella, Chiara A.</creator><creator>Fazio, Nicola</creator><creator>Valle, Juan W.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M3G</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170301</creationdate><title>HER2/HER3 pathway in biliary tract malignancies; systematic review and meta-analysis: a potential therapeutic target?</title><author>Galdy, Salvatore ; Lamarca, Angela ; McNamara, Mairéad G. ; Hubner, Richard A. ; Cella, Chiara A. ; Fazio, Nicola ; Valle, Juan W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c663t-de264dca7f65989ec7f7a0d4e97e84bd18b32e3170d046dec5bbb13ce6776ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Analysis</topic><topic>Biliary Tract Neoplasms - enzymology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Database searching</topic><topic>Epidermal growth factor</topic><topic>Genetic research</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Internet/Web search services</topic><topic>Metabolic Networks and Pathways</topic><topic>Non-Thematic Review</topic><topic>Oncology</topic><topic>Oncology, Experimental</topic><topic>Online searching</topic><topic>Receptor, ErbB-2 - biosynthesis</topic><topic>Receptor, ErbB-2 - genetics</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Receptor, ErbB-3 - biosynthesis</topic><topic>Receptor, ErbB-3 - genetics</topic><topic>Receptor, ErbB-3 - metabolism</topic><topic>Stomach cancer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Galdy, Salvatore</creatorcontrib><creatorcontrib>Lamarca, Angela</creatorcontrib><creatorcontrib>McNamara, Mairéad G.</creatorcontrib><creatorcontrib>Hubner, Richard A.</creatorcontrib><creatorcontrib>Cella, Chiara A.</creatorcontrib><creatorcontrib>Fazio, Nicola</creatorcontrib><creatorcontrib>Valle, Juan W.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>CBCA Reference & Current Events</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer and metastasis reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Galdy, Salvatore</au><au>Lamarca, Angela</au><au>McNamara, Mairéad G.</au><au>Hubner, Richard A.</au><au>Cella, Chiara A.</au><au>Fazio, Nicola</au><au>Valle, Juan W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HER2/HER3 pathway in biliary tract malignancies; systematic review and meta-analysis: a potential therapeutic target?</atitle><jtitle>Cancer and metastasis reviews</jtitle><stitle>Cancer Metastasis Rev</stitle><addtitle>Cancer Metastasis Rev</addtitle><date>2017-03-01</date><risdate>2017</risdate><volume>36</volume><issue>1</issue><spage>141</spage><epage>157</epage><pages>141-157</pages><issn>0167-7659</issn><eissn>1573-7233</eissn><coden>CMRED4</coden><abstract>Human epidermal growth factor receptor 2 (HER2) overexpression and amplification have been reported as predictive markers for HER2-targeted therapy in breast and gastric cancer, whereas human epidermal growth factor receptor 3 (HER3) is emerging as a potential resistance factor. The aim of this study was to perform a systematic review and meta-analysis of the HER2 and HER3 overexpression and amplification in biliary tract cancers (BTCs). An electronic search of MEDLINE, American Society of Clinical Oncology (ASCO), European Society of Medical Oncology Congress (ESMO), and American Association for Cancer Research (AACR) was performed to identify studies reporting HER2 and/or HER3 membrane protein expression by immunohistochemistry (IHC) and/or gene amplification by
in situ
hybridization (ISH) in BTCs. Studies were classified as “high quality” (HQ) if IHC overexpression was defined as presence of moderate/strong staining or “low quality” (LQ) where “any” expression was considered positive. Of 440 studies screened, 40 met the inclusion criteria. Globally, HER2 expression rate was 26.5 % (95 % CI 18.9–34.1 %). When HQ studies were analyzed (
n
= 27 studies), extrahepatic BTCs showed a higher HER2 overexpression rate compared to intrahepatic cholangiocarcinoma: 19.9 % (95 % CI 12.8–27.1 %) vs. 4.8 % (95 % CI 0–14.5 %), respectively,
p
value 0.0049. HER2 amplification rate was higher in patients selected by HER2 overexpression compared to “unselected” patients: 57.6 % (95 % CI 16.2–99 %) vs. 17.9 % (95 % CI 0.1–35.4 %), respectively,
p
value 0.0072. HER3 overexpression (4/4 HQ studies) and amplification rates were 27.9 % (95 % CI 9.7–46.1 %) and 26.5 % (one study), respectively. Up to 20 % of extrahepatic BTCs appear to be HER2 overexpressed; of these, close to 60 % appear to be HER2 amplified, while HER3 is overexpressed or amplified in about 25 % of patients. Clinical relevance for targeted therapy should be tested in prospective clinical trials.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>27981460</pmid><doi>10.1007/s10555-016-9645-x</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Biliary Tract Neoplasms - enzymology Biomedical and Life Sciences Biomedicine Cancer Cancer Research Database searching Epidermal growth factor Genetic research Health aspects Humans Immunohistochemistry Internet/Web search services Metabolic Networks and Pathways Non-Thematic Review Oncology Oncology, Experimental Online searching Receptor, ErbB-2 - biosynthesis Receptor, ErbB-2 - genetics Receptor, ErbB-2 - metabolism Receptor, ErbB-3 - biosynthesis Receptor, ErbB-3 - genetics Receptor, ErbB-3 - metabolism Stomach cancer |
title | HER2/HER3 pathway in biliary tract malignancies; systematic review and meta-analysis: a potential therapeutic target? |
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