Biologic and Clinical Characteristics of Breast Cancer With Single Hormone Receptor–Positive Phenotype
Response to endocrine therapy in breast cancer correlates with estrogen receptor (ER) and progesterone receptor (PgR) status. It is usually easier to decide treatment strategies in cases of double-positive/-negative phenotypes than in single-positive tumors. We have examined a large and well-charact...
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Veröffentlicht in: | Journal of clinical oncology 2007-10, Vol.25 (30), p.4772-4778 |
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creator | RAKHA, Emad A EL-SAYED, Maysa E GREEN, Andrew R PAISH, E. Claire POWE, Desmond G GEE, Julia NICHOLSON, Robert I LEE, Andrew H. S ROBERTSON, John F. R ELLIS, Ian O |
description | Response to endocrine therapy in breast cancer correlates with estrogen receptor (ER) and progesterone receptor (PgR) status. It is usually easier to decide treatment strategies in cases of double-positive/-negative phenotypes than in single-positive tumors.
We have examined a large and well-characterized series of primary invasive breast carcinoma (1,944 cases) with long-term clinical follow-up and hormone therapy data. Patients were stratified according to ER and PgR expression and the study was focused on the single-positive groups (ER-/PgR+ and ER+/PgR-), to assess their main features and evaluate any prognostic and predictive difference between them and compare them with the double-positive/-negative tumors.
ER+/PgR-tumors were found more frequently in elderly, postmenopausal women. The majority were grade 2 ductal/no specific type carcinomas. There was no difference between the two groups with regard to lymph node stage. Survival analyses showed no difference between the two groups in terms of disease-free interval and overall survival. However, when compared with the double-negative phenotype, ER+/PgR-showed an association with better outcome but no such survival advantage was detected in case of ER-/PgR+ tumors. In the group of patients with ER+ tumors who received adjuvant hormonal therapy, absence of PgR (ER+/PgR-) was an independent predictor of development of recurrence and shorter survival and, hence, poorer response to hormonal therapy.
ER+/PgR-and ER-/PgR+ tumors are biologically and clinically distinct groups of breast cancer that may require different treatment strategies with ER-/PgR+ exhibiting more aggressive behavioral characteristics. |
doi_str_mv | 10.1200/JCO.2007.12.2747 |
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We have examined a large and well-characterized series of primary invasive breast carcinoma (1,944 cases) with long-term clinical follow-up and hormone therapy data. Patients were stratified according to ER and PgR expression and the study was focused on the single-positive groups (ER-/PgR+ and ER+/PgR-), to assess their main features and evaluate any prognostic and predictive difference between them and compare them with the double-positive/-negative tumors.
ER+/PgR-tumors were found more frequently in elderly, postmenopausal women. The majority were grade 2 ductal/no specific type carcinomas. There was no difference between the two groups with regard to lymph node stage. Survival analyses showed no difference between the two groups in terms of disease-free interval and overall survival. However, when compared with the double-negative phenotype, ER+/PgR-showed an association with better outcome but no such survival advantage was detected in case of ER-/PgR+ tumors. In the group of patients with ER+ tumors who received adjuvant hormonal therapy, absence of PgR (ER+/PgR-) was an independent predictor of development of recurrence and shorter survival and, hence, poorer response to hormonal therapy.
ER+/PgR-and ER-/PgR+ tumors are biologically and clinically distinct groups of breast cancer that may require different treatment strategies with ER-/PgR+ exhibiting more aggressive behavioral characteristics.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2007.12.2747</identifier><identifier>PMID: 17876012</identifier><language>eng</language><publisher>Baltimore, MD: American Society of Clinical Oncology</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Female ; Gynecology. Andrology. Obstetrics ; Humans ; Immunoenzyme Techniques ; Lymphatic Metastasis ; Mammary gland diseases ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness - pathology ; Neoplasm Recurrence, Local - drug therapy ; Neoplasm Recurrence, Local - metabolism ; Neoplasm Recurrence, Local - pathology ; Neoplasm Staging ; Neoplasms, Hormone-Dependent - drug therapy ; Neoplasms, Hormone-Dependent - metabolism ; Neoplasms, Hormone-Dependent - pathology ; Prognosis ; Receptors, Estrogen - metabolism ; Receptors, Progesterone - metabolism ; Survival Rate ; Treatment Outcome ; Tumors</subject><ispartof>Journal of clinical oncology, 2007-10, Vol.25 (30), p.4772-4778</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-9fec445034a6aee6db7f7425eeea1edfc5734efac19a86ab05e24b1ac5f39bdf3</citedby><cites>FETCH-LOGICAL-c359t-9fec445034a6aee6db7f7425eeea1edfc5734efac19a86ab05e24b1ac5f39bdf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3716,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19195433$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17876012$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>RAKHA, Emad A</creatorcontrib><creatorcontrib>EL-SAYED, Maysa E</creatorcontrib><creatorcontrib>GREEN, Andrew R</creatorcontrib><creatorcontrib>PAISH, E. Claire</creatorcontrib><creatorcontrib>POWE, Desmond G</creatorcontrib><creatorcontrib>GEE, Julia</creatorcontrib><creatorcontrib>NICHOLSON, Robert I</creatorcontrib><creatorcontrib>LEE, Andrew H. S</creatorcontrib><creatorcontrib>ROBERTSON, John F. R</creatorcontrib><creatorcontrib>ELLIS, Ian O</creatorcontrib><title>Biologic and Clinical Characteristics of Breast Cancer With Single Hormone Receptor–Positive Phenotype</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Response to endocrine therapy in breast cancer correlates with estrogen receptor (ER) and progesterone receptor (PgR) status. It is usually easier to decide treatment strategies in cases of double-positive/-negative phenotypes than in single-positive tumors.
We have examined a large and well-characterized series of primary invasive breast carcinoma (1,944 cases) with long-term clinical follow-up and hormone therapy data. Patients were stratified according to ER and PgR expression and the study was focused on the single-positive groups (ER-/PgR+ and ER+/PgR-), to assess their main features and evaluate any prognostic and predictive difference between them and compare them with the double-positive/-negative tumors.
ER+/PgR-tumors were found more frequently in elderly, postmenopausal women. The majority were grade 2 ductal/no specific type carcinomas. There was no difference between the two groups with regard to lymph node stage. Survival analyses showed no difference between the two groups in terms of disease-free interval and overall survival. However, when compared with the double-negative phenotype, ER+/PgR-showed an association with better outcome but no such survival advantage was detected in case of ER-/PgR+ tumors. In the group of patients with ER+ tumors who received adjuvant hormonal therapy, absence of PgR (ER+/PgR-) was an independent predictor of development of recurrence and shorter survival and, hence, poorer response to hormonal therapy.
ER+/PgR-and ER-/PgR+ tumors are biologically and clinically distinct groups of breast cancer that may require different treatment strategies with ER-/PgR+ exhibiting more aggressive behavioral characteristics.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Lymphatic Metastasis</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Neoplasm Recurrence, Local - drug therapy</subject><subject>Neoplasm Recurrence, Local - metabolism</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Staging</subject><subject>Neoplasms, Hormone-Dependent - drug therapy</subject><subject>Neoplasms, Hormone-Dependent - metabolism</subject><subject>Neoplasms, Hormone-Dependent - pathology</subject><subject>Prognosis</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Survival Rate</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1u1DAYRS1ERYfCnhXyBlhl8G-cLGkEFFSpFT-CneU4nyeunHiwM1Td9R14Q56kHs1IXV1d6dy7OAi9omRNGSHvv3ZX65KqtDVTQj1BKyqZqpSS8ilaEcVZRRv--xQ9z_mGECoaLp-hU6oaVRPKVmg89zHEjbfYzAPugp-9NQF3o0nGLpB8XrzNODp8nsDkBXdmtpDwL7-M-LufNwHwRUxTnAF_AwvbJab_9_-uY_aL_wv4eoQ5LndbeIFOnAkZXh7zDP389PFHd1FdXn3-0n24rCyX7VK1DqwQknBhagNQD71ySjAJAIbC4KxUXIAzlramqU1PJDDRU2Ol420_OH6G3h5-tyn-2UFe9OSzhRDMDHGXdd0IohpZF5AcQJtizgmc3iY_mXSnKdF7u7rY1Xu7pem93TJ5ffze9RMMj4OjzgK8OQImF40uFVk-P3ItbaXgvHDvDtzoN-OtT6DzZEIot0zf2Mik5kQLpRh_AAE_kuQ</recordid><startdate>20071020</startdate><enddate>20071020</enddate><creator>RAKHA, Emad A</creator><creator>EL-SAYED, Maysa E</creator><creator>GREEN, Andrew R</creator><creator>PAISH, E. Claire</creator><creator>POWE, Desmond G</creator><creator>GEE, Julia</creator><creator>NICHOLSON, Robert I</creator><creator>LEE, Andrew H. S</creator><creator>ROBERTSON, John F. R</creator><creator>ELLIS, Ian O</creator><general>American Society of Clinical Oncology</general><general>Lippincott Williams & Wilkins</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20071020</creationdate><title>Biologic and Clinical Characteristics of Breast Cancer With Single Hormone Receptor–Positive Phenotype</title><author>RAKHA, Emad A ; EL-SAYED, Maysa E ; GREEN, Andrew R ; PAISH, E. Claire ; POWE, Desmond G ; GEE, Julia ; NICHOLSON, Robert I ; LEE, Andrew H. S ; ROBERTSON, John F. 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Obstetrics</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Lymphatic Metastasis</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>Neoplasm Recurrence, Local - drug therapy</topic><topic>Neoplasm Recurrence, Local - metabolism</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Staging</topic><topic>Neoplasms, Hormone-Dependent - drug therapy</topic><topic>Neoplasms, Hormone-Dependent - metabolism</topic><topic>Neoplasms, Hormone-Dependent - pathology</topic><topic>Prognosis</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Survival Rate</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>RAKHA, Emad A</creatorcontrib><creatorcontrib>EL-SAYED, Maysa E</creatorcontrib><creatorcontrib>GREEN, Andrew R</creatorcontrib><creatorcontrib>PAISH, E. Claire</creatorcontrib><creatorcontrib>POWE, Desmond G</creatorcontrib><creatorcontrib>GEE, Julia</creatorcontrib><creatorcontrib>NICHOLSON, Robert I</creatorcontrib><creatorcontrib>LEE, Andrew H. S</creatorcontrib><creatorcontrib>ROBERTSON, John F. R</creatorcontrib><creatorcontrib>ELLIS, Ian O</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>RAKHA, Emad A</au><au>EL-SAYED, Maysa E</au><au>GREEN, Andrew R</au><au>PAISH, E. Claire</au><au>POWE, Desmond G</au><au>GEE, Julia</au><au>NICHOLSON, Robert I</au><au>LEE, Andrew H. S</au><au>ROBERTSON, John F. R</au><au>ELLIS, Ian O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biologic and Clinical Characteristics of Breast Cancer With Single Hormone Receptor–Positive Phenotype</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2007-10-20</date><risdate>2007</risdate><volume>25</volume><issue>30</issue><spage>4772</spage><epage>4778</epage><pages>4772-4778</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Response to endocrine therapy in breast cancer correlates with estrogen receptor (ER) and progesterone receptor (PgR) status. It is usually easier to decide treatment strategies in cases of double-positive/-negative phenotypes than in single-positive tumors.
We have examined a large and well-characterized series of primary invasive breast carcinoma (1,944 cases) with long-term clinical follow-up and hormone therapy data. Patients were stratified according to ER and PgR expression and the study was focused on the single-positive groups (ER-/PgR+ and ER+/PgR-), to assess their main features and evaluate any prognostic and predictive difference between them and compare them with the double-positive/-negative tumors.
ER+/PgR-tumors were found more frequently in elderly, postmenopausal women. The majority were grade 2 ductal/no specific type carcinomas. There was no difference between the two groups with regard to lymph node stage. Survival analyses showed no difference between the two groups in terms of disease-free interval and overall survival. However, when compared with the double-negative phenotype, ER+/PgR-showed an association with better outcome but no such survival advantage was detected in case of ER-/PgR+ tumors. In the group of patients with ER+ tumors who received adjuvant hormonal therapy, absence of PgR (ER+/PgR-) was an independent predictor of development of recurrence and shorter survival and, hence, poorer response to hormonal therapy.
ER+/PgR-and ER-/PgR+ tumors are biologically and clinically distinct groups of breast cancer that may require different treatment strategies with ER-/PgR+ exhibiting more aggressive behavioral characteristics.</abstract><cop>Baltimore, MD</cop><pub>American Society of Clinical Oncology</pub><pmid>17876012</pmid><doi>10.1200/JCO.2007.12.2747</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Breast Neoplasms - pathology Female Gynecology. Andrology. Obstetrics Humans Immunoenzyme Techniques Lymphatic Metastasis Mammary gland diseases Medical sciences Middle Aged Neoplasm Invasiveness - pathology Neoplasm Recurrence, Local - drug therapy Neoplasm Recurrence, Local - metabolism Neoplasm Recurrence, Local - pathology Neoplasm Staging Neoplasms, Hormone-Dependent - drug therapy Neoplasms, Hormone-Dependent - metabolism Neoplasms, Hormone-Dependent - pathology Prognosis Receptors, Estrogen - metabolism Receptors, Progesterone - metabolism Survival Rate Treatment Outcome Tumors |
title | Biologic and Clinical Characteristics of Breast Cancer With Single Hormone Receptor–Positive Phenotype |
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