PTEN Loss Is Associated with Worse Outcome in HER2-Amplified Breast Cancer Patients but Is Not Associated with Trastuzumab Resistance
To investigate the clinical relevance of PTEN in HER2-amplified and HER2-nonamplified disease. We assessed PTEN status in two large adjuvant breast cancer trials (BCIRG-006 and BCIRG-005) using a PTEN immunohistochemical (IHC) assay that was previously validated in a panel of 33 breast cancer cell l...
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Veröffentlicht in: | Clinical cancer research 2015-05, Vol.21 (9), p.2065-2074 |
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creator | Stern, Howard M Gardner, Humphrey Burzykowski, Tomasz Elatre, Wafaa O'Brien, Carol Lackner, Mark R Pestano, Gary A Santiago, Angela Villalobos, Ivonne Eiermann, Wolfgang Pienkowski, Tadeusz Martin, Miguel Robert, Nicholas Crown, John Nuciforo, Paolo Bee, Valerie Mackey, John Slamon, Dennis J Press, Michael F |
description | To investigate the clinical relevance of PTEN in HER2-amplified and HER2-nonamplified disease.
We assessed PTEN status in two large adjuvant breast cancer trials (BCIRG-006 and BCIRG-005) using a PTEN immunohistochemical (IHC) assay that was previously validated in a panel of 33 breast cancer cell lines and prostate cancer tissues with known PTEN gene deletion.
In the HER2-positive patient population, absence of tumor cell PTEN staining occurred at a rate of 5.4% and was independent of ER/PR status. In contrast, 15.9% of HER2-negative patients exhibited absence of PTEN staining with the highest frequency seen in triple-negative breast cancer (TNBC) subgroup versus ER/PR-positive patients (35.1% vs. 10.9%). Complete absence of PTEN staining in tumor cells was associated with poor clinical outcome in HER2-positive disease. Those patients whose cancers demonstrated absent PTEN staining had a significant decrease in disease-free survival (DFS) and overall survival (OS) compared with patients with tumors exhibiting any PTEN staining patterns (low, moderate, or high). Trastuzumab appeared to provide clinical benefit even for patients lacking PTEN staining. In the HER2-negative population, there were no statistically significant differences in clinical outcome based on PTEN status.
This study is the largest to date examining PTEN status in breast cancer and the data suggest that the rate and significance of PTEN status differ between HER2-positive and HER2-negative disease. Furthermore, the data clearly suggest that HER2-positive patients with PTEN loss still benefit from trastuzumab. |
doi_str_mv | 10.1158/1078-0432.CCR-14-2993 |
format | Article |
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We assessed PTEN status in two large adjuvant breast cancer trials (BCIRG-006 and BCIRG-005) using a PTEN immunohistochemical (IHC) assay that was previously validated in a panel of 33 breast cancer cell lines and prostate cancer tissues with known PTEN gene deletion.
In the HER2-positive patient population, absence of tumor cell PTEN staining occurred at a rate of 5.4% and was independent of ER/PR status. In contrast, 15.9% of HER2-negative patients exhibited absence of PTEN staining with the highest frequency seen in triple-negative breast cancer (TNBC) subgroup versus ER/PR-positive patients (35.1% vs. 10.9%). Complete absence of PTEN staining in tumor cells was associated with poor clinical outcome in HER2-positive disease. Those patients whose cancers demonstrated absent PTEN staining had a significant decrease in disease-free survival (DFS) and overall survival (OS) compared with patients with tumors exhibiting any PTEN staining patterns (low, moderate, or high). Trastuzumab appeared to provide clinical benefit even for patients lacking PTEN staining. In the HER2-negative population, there were no statistically significant differences in clinical outcome based on PTEN status.
This study is the largest to date examining PTEN status in breast cancer and the data suggest that the rate and significance of PTEN status differ between HER2-positive and HER2-negative disease. Furthermore, the data clearly suggest that HER2-positive patients with PTEN loss still benefit from trastuzumab.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-14-2993</identifier><identifier>PMID: 25649019</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Aged ; Antineoplastic Agents - therapeutic use ; Breast Neoplasms - drug therapy ; Breast Neoplasms - genetics ; Breast Neoplasms - mortality ; Drug Resistance, Neoplasm - genetics ; Female ; Humans ; Immunohistochemistry ; Kaplan-Meier Estimate ; Middle Aged ; Proportional Hazards Models ; PTEN Phosphohydrolase - genetics ; Receptor, ErbB-2 - genetics ; Tissue Array Analysis ; Trastuzumab - therapeutic use</subject><ispartof>Clinical cancer research, 2015-05, Vol.21 (9), p.2065-2074</ispartof><rights>2015 American Association for Cancer Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-9515ad947b4c0d952aeacab041e74a2ef6e4c32c0bc26f414d6e2248b8775a5e3</citedby><cites>FETCH-LOGICAL-c463t-9515ad947b4c0d952aeacab041e74a2ef6e4c32c0bc26f414d6e2248b8775a5e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3342,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25649019$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stern, Howard M</creatorcontrib><creatorcontrib>Gardner, Humphrey</creatorcontrib><creatorcontrib>Burzykowski, Tomasz</creatorcontrib><creatorcontrib>Elatre, Wafaa</creatorcontrib><creatorcontrib>O'Brien, Carol</creatorcontrib><creatorcontrib>Lackner, Mark R</creatorcontrib><creatorcontrib>Pestano, Gary A</creatorcontrib><creatorcontrib>Santiago, Angela</creatorcontrib><creatorcontrib>Villalobos, Ivonne</creatorcontrib><creatorcontrib>Eiermann, Wolfgang</creatorcontrib><creatorcontrib>Pienkowski, Tadeusz</creatorcontrib><creatorcontrib>Martin, Miguel</creatorcontrib><creatorcontrib>Robert, Nicholas</creatorcontrib><creatorcontrib>Crown, John</creatorcontrib><creatorcontrib>Nuciforo, Paolo</creatorcontrib><creatorcontrib>Bee, Valerie</creatorcontrib><creatorcontrib>Mackey, John</creatorcontrib><creatorcontrib>Slamon, Dennis J</creatorcontrib><creatorcontrib>Press, Michael F</creatorcontrib><title>PTEN Loss Is Associated with Worse Outcome in HER2-Amplified Breast Cancer Patients but Is Not Associated with Trastuzumab Resistance</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>To investigate the clinical relevance of PTEN in HER2-amplified and HER2-nonamplified disease.
We assessed PTEN status in two large adjuvant breast cancer trials (BCIRG-006 and BCIRG-005) using a PTEN immunohistochemical (IHC) assay that was previously validated in a panel of 33 breast cancer cell lines and prostate cancer tissues with known PTEN gene deletion.
In the HER2-positive patient population, absence of tumor cell PTEN staining occurred at a rate of 5.4% and was independent of ER/PR status. In contrast, 15.9% of HER2-negative patients exhibited absence of PTEN staining with the highest frequency seen in triple-negative breast cancer (TNBC) subgroup versus ER/PR-positive patients (35.1% vs. 10.9%). Complete absence of PTEN staining in tumor cells was associated with poor clinical outcome in HER2-positive disease. Those patients whose cancers demonstrated absent PTEN staining had a significant decrease in disease-free survival (DFS) and overall survival (OS) compared with patients with tumors exhibiting any PTEN staining patterns (low, moderate, or high). Trastuzumab appeared to provide clinical benefit even for patients lacking PTEN staining. In the HER2-negative population, there were no statistically significant differences in clinical outcome based on PTEN status.
This study is the largest to date examining PTEN status in breast cancer and the data suggest that the rate and significance of PTEN status differ between HER2-positive and HER2-negative disease. Furthermore, the data clearly suggest that HER2-positive patients with PTEN loss still benefit from trastuzumab.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - mortality</subject><subject>Drug Resistance, Neoplasm - genetics</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kaplan-Meier Estimate</subject><subject>Middle Aged</subject><subject>Proportional Hazards Models</subject><subject>PTEN Phosphohydrolase - genetics</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>Tissue Array Analysis</subject><subject>Trastuzumab - therapeutic use</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkc1u1DAUhS0Eoj_wCCAv2aS1HTuON0hDNKWVRm01GsTScpwbapTEg-0U0T3vXUf9URErW_I5n6_uh9AHSk4oFfUpJbIuCC_ZSdNsC8oLplT5Ch1SIWRRskq8zvenzAE6ivEnIZRTwt-iAyYqrghVh-jv9W59iTc-RnwR8SpGb51J0OHfLt3g7z5EwFdzsn4E7CZ8vt6yYjXuB9e7HPoSwMSEGzNZCPjaJAdTirid00K79Ok_4i7kwnw3j6bFW4gupqX7Dr3pzRDh_eN5jL6drXfNebG5-nrRrDaF5VWZCiWoMJ3isuWWdEowA8aalnAKkhsGfQXclsyS1rKq55R3FTDG67aWUhgB5TH6_MDdz-0Inc3TBjPofXCjCX-0N07_-zK5G_3D32rOqeRUZcCnR0Dwv2aISY8uWhgGM4Gfo6aVlHWtREVyVDxEbcjbDdA_f0OJXhTqRY9e9OisUFOuF4W59_HljM-tJ2flPXWqmaw</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Stern, Howard M</creator><creator>Gardner, Humphrey</creator><creator>Burzykowski, Tomasz</creator><creator>Elatre, Wafaa</creator><creator>O'Brien, Carol</creator><creator>Lackner, Mark R</creator><creator>Pestano, Gary A</creator><creator>Santiago, Angela</creator><creator>Villalobos, Ivonne</creator><creator>Eiermann, Wolfgang</creator><creator>Pienkowski, Tadeusz</creator><creator>Martin, Miguel</creator><creator>Robert, Nicholas</creator><creator>Crown, John</creator><creator>Nuciforo, Paolo</creator><creator>Bee, Valerie</creator><creator>Mackey, John</creator><creator>Slamon, Dennis J</creator><creator>Press, Michael F</creator><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150501</creationdate><title>PTEN Loss Is Associated with Worse Outcome in HER2-Amplified Breast Cancer Patients but Is Not Associated with Trastuzumab Resistance</title><author>Stern, Howard M ; Gardner, Humphrey ; Burzykowski, Tomasz ; Elatre, Wafaa ; O'Brien, Carol ; Lackner, Mark R ; Pestano, Gary A ; Santiago, Angela ; Villalobos, Ivonne ; Eiermann, Wolfgang ; Pienkowski, Tadeusz ; Martin, Miguel ; Robert, Nicholas ; Crown, John ; Nuciforo, Paolo ; Bee, Valerie ; Mackey, John ; Slamon, Dennis J ; Press, Michael F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-9515ad947b4c0d952aeacab041e74a2ef6e4c32c0bc26f414d6e2248b8775a5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - mortality</topic><topic>Drug Resistance, Neoplasm - genetics</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kaplan-Meier Estimate</topic><topic>Middle Aged</topic><topic>Proportional Hazards Models</topic><topic>PTEN Phosphohydrolase - genetics</topic><topic>Receptor, ErbB-2 - genetics</topic><topic>Tissue Array Analysis</topic><topic>Trastuzumab - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stern, Howard M</creatorcontrib><creatorcontrib>Gardner, Humphrey</creatorcontrib><creatorcontrib>Burzykowski, Tomasz</creatorcontrib><creatorcontrib>Elatre, Wafaa</creatorcontrib><creatorcontrib>O'Brien, Carol</creatorcontrib><creatorcontrib>Lackner, Mark R</creatorcontrib><creatorcontrib>Pestano, Gary A</creatorcontrib><creatorcontrib>Santiago, Angela</creatorcontrib><creatorcontrib>Villalobos, Ivonne</creatorcontrib><creatorcontrib>Eiermann, Wolfgang</creatorcontrib><creatorcontrib>Pienkowski, Tadeusz</creatorcontrib><creatorcontrib>Martin, Miguel</creatorcontrib><creatorcontrib>Robert, Nicholas</creatorcontrib><creatorcontrib>Crown, John</creatorcontrib><creatorcontrib>Nuciforo, Paolo</creatorcontrib><creatorcontrib>Bee, Valerie</creatorcontrib><creatorcontrib>Mackey, John</creatorcontrib><creatorcontrib>Slamon, Dennis J</creatorcontrib><creatorcontrib>Press, Michael F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stern, Howard M</au><au>Gardner, Humphrey</au><au>Burzykowski, Tomasz</au><au>Elatre, Wafaa</au><au>O'Brien, Carol</au><au>Lackner, Mark R</au><au>Pestano, Gary A</au><au>Santiago, Angela</au><au>Villalobos, Ivonne</au><au>Eiermann, Wolfgang</au><au>Pienkowski, Tadeusz</au><au>Martin, Miguel</au><au>Robert, Nicholas</au><au>Crown, John</au><au>Nuciforo, Paolo</au><au>Bee, Valerie</au><au>Mackey, John</au><au>Slamon, Dennis J</au><au>Press, Michael F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PTEN Loss Is Associated with Worse Outcome in HER2-Amplified Breast Cancer Patients but Is Not Associated with Trastuzumab Resistance</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>21</volume><issue>9</issue><spage>2065</spage><epage>2074</epage><pages>2065-2074</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>To investigate the clinical relevance of PTEN in HER2-amplified and HER2-nonamplified disease.
We assessed PTEN status in two large adjuvant breast cancer trials (BCIRG-006 and BCIRG-005) using a PTEN immunohistochemical (IHC) assay that was previously validated in a panel of 33 breast cancer cell lines and prostate cancer tissues with known PTEN gene deletion.
In the HER2-positive patient population, absence of tumor cell PTEN staining occurred at a rate of 5.4% and was independent of ER/PR status. In contrast, 15.9% of HER2-negative patients exhibited absence of PTEN staining with the highest frequency seen in triple-negative breast cancer (TNBC) subgroup versus ER/PR-positive patients (35.1% vs. 10.9%). Complete absence of PTEN staining in tumor cells was associated with poor clinical outcome in HER2-positive disease. Those patients whose cancers demonstrated absent PTEN staining had a significant decrease in disease-free survival (DFS) and overall survival (OS) compared with patients with tumors exhibiting any PTEN staining patterns (low, moderate, or high). Trastuzumab appeared to provide clinical benefit even for patients lacking PTEN staining. In the HER2-negative population, there were no statistically significant differences in clinical outcome based on PTEN status.
This study is the largest to date examining PTEN status in breast cancer and the data suggest that the rate and significance of PTEN status differ between HER2-positive and HER2-negative disease. Furthermore, the data clearly suggest that HER2-positive patients with PTEN loss still benefit from trastuzumab.</abstract><cop>United States</cop><pmid>25649019</pmid><doi>10.1158/1078-0432.CCR-14-2993</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Adult Aged Antineoplastic Agents - therapeutic use Breast Neoplasms - drug therapy Breast Neoplasms - genetics Breast Neoplasms - mortality Drug Resistance, Neoplasm - genetics Female Humans Immunohistochemistry Kaplan-Meier Estimate Middle Aged Proportional Hazards Models PTEN Phosphohydrolase - genetics Receptor, ErbB-2 - genetics Tissue Array Analysis Trastuzumab - therapeutic use |
title | PTEN Loss Is Associated with Worse Outcome in HER2-Amplified Breast Cancer Patients but Is Not Associated with Trastuzumab Resistance |
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