Clinicopathological significance of androgen receptor, HER2, Ki-67 and EGFR expressions in salivary duct carcinoma
Background Salivary duct carcinoma (SDC) is a highly aggressive disease which often metastasizes to distant sites, and there is no established standard therapy for this systemic disease. Given that SDC is biologically similar to breast and prostate cancer, anti-androgenic receptor (AR) and anti-huma...
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creator | Masubuchi, Tatsuo Tada, Yuichiro Maruya, Shin-ichiro Osamura, Yoshiyuki Kamata, Shin-etsu Miura, Kouki Fushimi, Chihiro Takahashi, Hideaki Kawakita, Daisuke Kishimoto, Seiji Nagao, Toshitaka |
description | Background
Salivary duct carcinoma (SDC) is a highly aggressive disease which often metastasizes to distant sites, and there is no established standard therapy for this systemic disease. Given that SDC is biologically similar to breast and prostate cancer, anti-androgenic receptor (AR) and anti-human epidermal growth factor receptor 2 (HER2) therapies have the potential to exert effects, not only on patients with breast and prostate cancer but also on those with SDC.
Methods
The expression levels of HER2, epidermal growth factor receptor (EGFR), Ki-67, and AR were assessed in 32 patients with SDC, and their correlations with overall survival (OS) and disease-free survival (DFS) were analyzed retrospectively. SDC was classified into five subtypes using a method similar to that used for breast cancer.
Results
Anti-AR, HER2, and EGFR were positive in 23 (71.9 %), 14 (43.8 %), and 26 (81.3 %) cases, respectively. One or more of these 3 factors were positive in 30 (93.8 %) cases. The Ki-67 labeling index was greater than 15 % in all cases. While molecular status did not correlate with OS, EGFR and AR positivity were significantly associated with DFS in univariate analysis. Multivariate analysis revealed that EGFR was the only independent predictor of DFS.
Conclusions
The statuses of some molecules are useful to predict DFS in patients with SDC. Ki-67 overexpression suggests that cytotoxic agents are effective for SDC. Since the majority of SDCs express AR, HER2, and/or EGFR, assessing and targeting these molecules are promising strategies to improve the prognosis of unresectable, metastatic or recurrent SDC, and a classification system according to the molecular expression status may be useful to select appropriate therapy. |
doi_str_mv | 10.1007/s10147-014-0674-6 |
format | Article |
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Salivary duct carcinoma (SDC) is a highly aggressive disease which often metastasizes to distant sites, and there is no established standard therapy for this systemic disease. Given that SDC is biologically similar to breast and prostate cancer, anti-androgenic receptor (AR) and anti-human epidermal growth factor receptor 2 (HER2) therapies have the potential to exert effects, not only on patients with breast and prostate cancer but also on those with SDC.
Methods
The expression levels of HER2, epidermal growth factor receptor (EGFR), Ki-67, and AR were assessed in 32 patients with SDC, and their correlations with overall survival (OS) and disease-free survival (DFS) were analyzed retrospectively. SDC was classified into five subtypes using a method similar to that used for breast cancer.
Results
Anti-AR, HER2, and EGFR were positive in 23 (71.9 %), 14 (43.8 %), and 26 (81.3 %) cases, respectively. One or more of these 3 factors were positive in 30 (93.8 %) cases. The Ki-67 labeling index was greater than 15 % in all cases. While molecular status did not correlate with OS, EGFR and AR positivity were significantly associated with DFS in univariate analysis. Multivariate analysis revealed that EGFR was the only independent predictor of DFS.
Conclusions
The statuses of some molecules are useful to predict DFS in patients with SDC. Ki-67 overexpression suggests that cytotoxic agents are effective for SDC. Since the majority of SDCs express AR, HER2, and/or EGFR, assessing and targeting these molecules are promising strategies to improve the prognosis of unresectable, metastatic or recurrent SDC, and a classification system according to the molecular expression status may be useful to select appropriate therapy.</description><identifier>ISSN: 1341-9625</identifier><identifier>EISSN: 1437-7772</identifier><identifier>DOI: 10.1007/s10147-014-0674-6</identifier><identifier>PMID: 24553861</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Cancer Research ; Disease-Free Survival ; Epidermal growth factor ; Exocrine glands ; Female ; Head & neck cancer ; Humans ; Ki-67 Antigen - metabolism ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Oncology ; Original Article ; Prognosis ; Protein expression ; Receptor, Epidermal Growth Factor - metabolism ; Receptor, ErbB-2 - metabolism ; Receptors, Androgen - metabolism ; Retrospective Studies ; Salivary Ducts - metabolism ; Salivary Ducts - pathology ; Salivary Gland Neoplasms - metabolism ; Salivary Gland Neoplasms - pathology ; Surgical Oncology</subject><ispartof>International journal of clinical oncology, 2015-02, Vol.20 (1), p.35-44</ispartof><rights>Japan Society of Clinical Oncology 2014</rights><rights>Japan Society of Clinical Oncology 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-9ec5865638d9de92efd4c725e88b18a93d161a18ac089bab19075cac5fb64c903</citedby><cites>FETCH-LOGICAL-c532t-9ec5865638d9de92efd4c725e88b18a93d161a18ac089bab19075cac5fb64c903</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/s10147-014-0674-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10147-014-0674-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24553861$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masubuchi, Tatsuo</creatorcontrib><creatorcontrib>Tada, Yuichiro</creatorcontrib><creatorcontrib>Maruya, Shin-ichiro</creatorcontrib><creatorcontrib>Osamura, Yoshiyuki</creatorcontrib><creatorcontrib>Kamata, Shin-etsu</creatorcontrib><creatorcontrib>Miura, Kouki</creatorcontrib><creatorcontrib>Fushimi, Chihiro</creatorcontrib><creatorcontrib>Takahashi, Hideaki</creatorcontrib><creatorcontrib>Kawakita, Daisuke</creatorcontrib><creatorcontrib>Kishimoto, Seiji</creatorcontrib><creatorcontrib>Nagao, Toshitaka</creatorcontrib><title>Clinicopathological significance of androgen receptor, HER2, Ki-67 and EGFR expressions in salivary duct carcinoma</title><title>International journal of clinical oncology</title><addtitle>Int J Clin Oncol</addtitle><addtitle>Int J Clin Oncol</addtitle><description>Background
Salivary duct carcinoma (SDC) is a highly aggressive disease which often metastasizes to distant sites, and there is no established standard therapy for this systemic disease. Given that SDC is biologically similar to breast and prostate cancer, anti-androgenic receptor (AR) and anti-human epidermal growth factor receptor 2 (HER2) therapies have the potential to exert effects, not only on patients with breast and prostate cancer but also on those with SDC.
Methods
The expression levels of HER2, epidermal growth factor receptor (EGFR), Ki-67, and AR were assessed in 32 patients with SDC, and their correlations with overall survival (OS) and disease-free survival (DFS) were analyzed retrospectively. SDC was classified into five subtypes using a method similar to that used for breast cancer.
Results
Anti-AR, HER2, and EGFR were positive in 23 (71.9 %), 14 (43.8 %), and 26 (81.3 %) cases, respectively. One or more of these 3 factors were positive in 30 (93.8 %) cases. The Ki-67 labeling index was greater than 15 % in all cases. While molecular status did not correlate with OS, EGFR and AR positivity were significantly associated with DFS in univariate analysis. Multivariate analysis revealed that EGFR was the only independent predictor of DFS.
Conclusions
The statuses of some molecules are useful to predict DFS in patients with SDC. Ki-67 overexpression suggests that cytotoxic agents are effective for SDC. Since the majority of SDCs express AR, HER2, and/or EGFR, assessing and targeting these molecules are promising strategies to improve the prognosis of unresectable, metastatic or recurrent SDC, and a classification system according to the molecular expression status may be useful to select appropriate therapy.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cancer Research</subject><subject>Disease-Free Survival</subject><subject>Epidermal growth factor</subject><subject>Exocrine glands</subject><subject>Female</subject><subject>Head & neck cancer</subject><subject>Humans</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Prognosis</subject><subject>Protein expression</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Receptors, Androgen - metabolism</subject><subject>Retrospective Studies</subject><subject>Salivary Ducts - metabolism</subject><subject>Salivary Ducts - pathology</subject><subject>Salivary Gland Neoplasms - metabolism</subject><subject>Salivary Gland Neoplasms - pathology</subject><subject>Surgical Oncology</subject><issn>1341-9625</issn><issn>1437-7772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kU1rFTEUhoMoba39AW4k4MZF0yaZfM1SLrcftCCUug6ZzJlrytxkTGZE_70ZbhURujl54Tx5T3JehN4zesEo1ZeFUSY0qYVQpQVRr9AJE40mWmv-uupGMNIqLo_R21KeKGVaSX6EjrmQsjGKnaC8GUMMPk1u_pbGtAvejbiEXQxDldEDTgN2sc9pBxFn8DDNKZ_jm-0DP8d3gSi9tvH2-uoBw88pQykhxYJDxMWN4YfLv3C_-Bl7l32Iae_eoTeDGwucPZ-n6OvV9nFzQ-6_XN9uPt8TLxs-kxa8NEqqxvRtDy2HoRdecwnGdMy4tumZYq4qT03buY61VEvvvBw6JXxLm1P06eA75fR9gTLbfSgextFFSEuxrO5CCCobVdGP_6FPacmxvm6lqKnrEqZS7ED5nErJMNgph339oGXUroHYQyC2FrsGYlfnD8_OS7eH_u-NPwlUgB-AUltxB_mf0S-6_gauhJUv</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Masubuchi, Tatsuo</creator><creator>Tada, Yuichiro</creator><creator>Maruya, Shin-ichiro</creator><creator>Osamura, Yoshiyuki</creator><creator>Kamata, Shin-etsu</creator><creator>Miura, Kouki</creator><creator>Fushimi, Chihiro</creator><creator>Takahashi, Hideaki</creator><creator>Kawakita, Daisuke</creator><creator>Kishimoto, Seiji</creator><creator>Nagao, Toshitaka</creator><general>Springer Japan</general><general>Springer Nature B.V</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>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>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150201</creationdate><title>Clinicopathological significance of androgen receptor, HER2, Ki-67 and EGFR expressions in salivary duct carcinoma</title><author>Masubuchi, Tatsuo ; Tada, Yuichiro ; Maruya, Shin-ichiro ; Osamura, Yoshiyuki ; Kamata, Shin-etsu ; Miura, Kouki ; Fushimi, Chihiro ; Takahashi, Hideaki ; Kawakita, Daisuke ; Kishimoto, Seiji ; Nagao, Toshitaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c532t-9ec5865638d9de92efd4c725e88b18a93d161a18ac089bab19075cac5fb64c903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cancer Research</topic><topic>Disease-Free Survival</topic><topic>Epidermal growth factor</topic><topic>Exocrine glands</topic><topic>Female</topic><topic>Head & neck cancer</topic><topic>Humans</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Prognosis</topic><topic>Protein expression</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Receptors, Androgen - metabolism</topic><topic>Retrospective Studies</topic><topic>Salivary Ducts - metabolism</topic><topic>Salivary Ducts - pathology</topic><topic>Salivary Gland Neoplasms - metabolism</topic><topic>Salivary Gland Neoplasms - pathology</topic><topic>Surgical Oncology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masubuchi, Tatsuo</creatorcontrib><creatorcontrib>Tada, Yuichiro</creatorcontrib><creatorcontrib>Maruya, Shin-ichiro</creatorcontrib><creatorcontrib>Osamura, Yoshiyuki</creatorcontrib><creatorcontrib>Kamata, Shin-etsu</creatorcontrib><creatorcontrib>Miura, Kouki</creatorcontrib><creatorcontrib>Fushimi, Chihiro</creatorcontrib><creatorcontrib>Takahashi, Hideaki</creatorcontrib><creatorcontrib>Kawakita, Daisuke</creatorcontrib><creatorcontrib>Kishimoto, Seiji</creatorcontrib><creatorcontrib>Nagao, Toshitaka</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 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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</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>ProQuest Central Student</collection><collection>Research Library Prep</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>Research Library</collection><collection>Research Library (Corporate)</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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masubuchi, Tatsuo</au><au>Tada, Yuichiro</au><au>Maruya, Shin-ichiro</au><au>Osamura, Yoshiyuki</au><au>Kamata, Shin-etsu</au><au>Miura, Kouki</au><au>Fushimi, Chihiro</au><au>Takahashi, Hideaki</au><au>Kawakita, Daisuke</au><au>Kishimoto, Seiji</au><au>Nagao, Toshitaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinicopathological significance of androgen receptor, HER2, Ki-67 and EGFR expressions in salivary duct carcinoma</atitle><jtitle>International journal of clinical oncology</jtitle><stitle>Int J Clin Oncol</stitle><addtitle>Int J Clin Oncol</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>20</volume><issue>1</issue><spage>35</spage><epage>44</epage><pages>35-44</pages><issn>1341-9625</issn><eissn>1437-7772</eissn><abstract>Background
Salivary duct carcinoma (SDC) is a highly aggressive disease which often metastasizes to distant sites, and there is no established standard therapy for this systemic disease. Given that SDC is biologically similar to breast and prostate cancer, anti-androgenic receptor (AR) and anti-human epidermal growth factor receptor 2 (HER2) therapies have the potential to exert effects, not only on patients with breast and prostate cancer but also on those with SDC.
Methods
The expression levels of HER2, epidermal growth factor receptor (EGFR), Ki-67, and AR were assessed in 32 patients with SDC, and their correlations with overall survival (OS) and disease-free survival (DFS) were analyzed retrospectively. SDC was classified into five subtypes using a method similar to that used for breast cancer.
Results
Anti-AR, HER2, and EGFR were positive in 23 (71.9 %), 14 (43.8 %), and 26 (81.3 %) cases, respectively. One or more of these 3 factors were positive in 30 (93.8 %) cases. The Ki-67 labeling index was greater than 15 % in all cases. While molecular status did not correlate with OS, EGFR and AR positivity were significantly associated with DFS in univariate analysis. Multivariate analysis revealed that EGFR was the only independent predictor of DFS.
Conclusions
The statuses of some molecules are useful to predict DFS in patients with SDC. Ki-67 overexpression suggests that cytotoxic agents are effective for SDC. Since the majority of SDCs express AR, HER2, and/or EGFR, assessing and targeting these molecules are promising strategies to improve the prognosis of unresectable, metastatic or recurrent SDC, and a classification system according to the molecular expression status may be useful to select appropriate therapy.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>24553861</pmid><doi>10.1007/s10147-014-0674-6</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Cancer Research Disease-Free Survival Epidermal growth factor Exocrine glands Female Head & neck cancer Humans Ki-67 Antigen - metabolism Male Medicine Medicine & Public Health Middle Aged Oncology Original Article Prognosis Protein expression Receptor, Epidermal Growth Factor - metabolism Receptor, ErbB-2 - metabolism Receptors, Androgen - metabolism Retrospective Studies Salivary Ducts - metabolism Salivary Ducts - pathology Salivary Gland Neoplasms - metabolism Salivary Gland Neoplasms - pathology Surgical Oncology |
title | Clinicopathological significance of androgen receptor, HER2, Ki-67 and EGFR expressions in salivary duct carcinoma |
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