Lack of prognostic value of epidermal growth factor receptor in a series of 229 T1/T2, N0/N1 breast cancers, with well defined prognostic parameters
The prognostic value of epidermal growth factor receptor (EGF-R) was prospectively assessed in a series of 229 clinical T1-T2, N0-N1 breast carcinomas diagnosed between May 1987 and October 1989. EGF-R expression was determined by measuring the specific Bmax of 125I EGF to tumor plasma membrane prep...
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Veröffentlicht in: | Breast cancer research and treatment 1994, Vol.29 (3), p.265-270 |
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creator | BOLLA, M CHEDIN, M COLONNA, M MARRON-CHARRIERE, J ROSTAING-PUISSANT, B PASQUIER, D PANH, M. H WINCKEL, P CHAMBAZ, E. M |
description | The prognostic value of epidermal growth factor receptor (EGF-R) was prospectively assessed in a series of 229 clinical T1-T2, N0-N1 breast carcinomas diagnosed between May 1987 and October 1989. EGF-R expression was determined by measuring the specific Bmax of 125I EGF to tumor plasma membrane preparations. Tumor with a Bmax > or = 3 fmol/mg of protein were considered positive with regard to EGF-R expression. With a median follow-up of 34 months, the 3-year overall and disease-free survivals are respectively 92% and 88% for EGF-R < or = 3, and 91% and 86% EGF-R > 3 fmol, showing no significant difference, even when comparing axillary lymph node status. We did not succeed in finding an EGF-R cut-off value which might be significant in univariate analysis. Multivariate analysis of our data indicates that pT (p = 0.001), pN (p = 0.04), and Scarff-Bloom grade (p = 0.04) are the only significant predictors of disease-free survival among the parameters investigated in this study. |
doi_str_mv | 10.1007/BF00666480 |
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Multivariate analysis of our data indicates that pT (p = 0.001), pN (p = 0.04), and Scarff-Bloom grade (p = 0.04) are the only significant predictors of disease-free survival among the parameters investigated in this study.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/BF00666480</identifier><identifier>PMID: 8049460</identifier><identifier>CODEN: BCTRD6</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Analysis of Variance ; Biological and medical sciences ; Breast Neoplasms - metabolism ; Breast Neoplasms - therapy ; Carcinoma - metabolism ; Carcinoma - therapy ; Combined Modality Therapy ; Epidermal Growth Factor - metabolism ; ErbB Receptors - metabolism ; Female ; Follow-Up Studies ; Gynecology. Andrology. 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H</creatorcontrib><creatorcontrib>WINCKEL, P</creatorcontrib><creatorcontrib>CHAMBAZ, E. M</creatorcontrib><title>Lack of prognostic value of epidermal growth factor receptor in a series of 229 T1/T2, N0/N1 breast cancers, with well defined prognostic parameters</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><description>The prognostic value of epidermal growth factor receptor (EGF-R) was prospectively assessed in a series of 229 clinical T1-T2, N0-N1 breast carcinomas diagnosed between May 1987 and October 1989. EGF-R expression was determined by measuring the specific Bmax of 125I EGF to tumor plasma membrane preparations. Tumor with a Bmax > or = 3 fmol/mg of protein were considered positive with regard to EGF-R expression. With a median follow-up of 34 months, the 3-year overall and disease-free survivals are respectively 92% and 88% for EGF-R < or = 3, and 91% and 86% EGF-R > 3 fmol, showing no significant difference, even when comparing axillary lymph node status. We did not succeed in finding an EGF-R cut-off value which might be significant in univariate analysis. Multivariate analysis of our data indicates that pT (p = 0.001), pN (p = 0.04), and Scarff-Bloom grade (p = 0.04) are the only significant predictors of disease-free survival among the parameters investigated in this study.</description><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - therapy</subject><subject>Carcinoma - metabolism</subject><subject>Carcinoma - therapy</subject><subject>Combined Modality Therapy</subject><subject>Epidermal Growth Factor - metabolism</subject><subject>ErbB Receptors - metabolism</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Survival Rate</subject><subject>Tumors</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkctOHDEQRa0oCAaSTfZIXkRZIJqp6ofdXhIUHtKIbCbrlu0uE0O_Yvcwyn_wwfGIEWFVpaqjW1e3GPuCcIEAcvn9GkAIUdbwgS2wkkUmc5Qf2QJQyEzUII7YcYyPAKAkqEN2WEOpSgEL9rLS9omPjk9hfBjGOHvLn3W3od2MJt9S6HXHH8K4nX9zp-08Bh7I0rRr_MA1jxQ8xR2f54qvcbnOz_k9LO-Rm0A6ztzqwVKI53zrk8iWuo635PxA7fuzkw66pzmBn9iB012kz_t6wn5d_1hf3Warnzd3V5erzBaIc6Yqg5VVtcWyLWsqnaGcpLKmFWQKY42tBJKqXS5dZRSiqKjVVWILB6IsihP27VU3ufizoTg3vY822dMDjZvYSCGwzguVwLNX0IYxxkCumYLvdfjbIDS7FzT_X5Dg073qxvTUvqH7zNP-636vo9WdCykdH9-wEiqJeV38A1vLjeA</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>BOLLA, M</creator><creator>CHEDIN, M</creator><creator>COLONNA, M</creator><creator>MARRON-CHARRIERE, J</creator><creator>ROSTAING-PUISSANT, B</creator><creator>PASQUIER, D</creator><creator>PANH, M. 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Obstetrics</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Survival Rate</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BOLLA, M</creatorcontrib><creatorcontrib>CHEDIN, M</creatorcontrib><creatorcontrib>COLONNA, M</creatorcontrib><creatorcontrib>MARRON-CHARRIERE, J</creatorcontrib><creatorcontrib>ROSTAING-PUISSANT, B</creatorcontrib><creatorcontrib>PASQUIER, D</creatorcontrib><creatorcontrib>PANH, M. H</creatorcontrib><creatorcontrib>WINCKEL, P</creatorcontrib><creatorcontrib>CHAMBAZ, E. 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M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lack of prognostic value of epidermal growth factor receptor in a series of 229 T1/T2, N0/N1 breast cancers, with well defined prognostic parameters</atitle><jtitle>Breast cancer research and treatment</jtitle><addtitle>Breast Cancer Res Treat</addtitle><date>1994</date><risdate>1994</risdate><volume>29</volume><issue>3</issue><spage>265</spage><epage>270</epage><pages>265-270</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><coden>BCTRD6</coden><abstract>The prognostic value of epidermal growth factor receptor (EGF-R) was prospectively assessed in a series of 229 clinical T1-T2, N0-N1 breast carcinomas diagnosed between May 1987 and October 1989. EGF-R expression was determined by measuring the specific Bmax of 125I EGF to tumor plasma membrane preparations. Tumor with a Bmax > or = 3 fmol/mg of protein were considered positive with regard to EGF-R expression. With a median follow-up of 34 months, the 3-year overall and disease-free survivals are respectively 92% and 88% for EGF-R < or = 3, and 91% and 86% EGF-R > 3 fmol, showing no significant difference, even when comparing axillary lymph node status. We did not succeed in finding an EGF-R cut-off value which might be significant in univariate analysis. Multivariate analysis of our data indicates that pT (p = 0.001), pN (p = 0.04), and Scarff-Bloom grade (p = 0.04) are the only significant predictors of disease-free survival among the parameters investigated in this study.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>8049460</pmid><doi>10.1007/BF00666480</doi><tpages>6</tpages></addata></record> |
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subjects | Analysis of Variance Biological and medical sciences Breast Neoplasms - metabolism Breast Neoplasms - therapy Carcinoma - metabolism Carcinoma - therapy Combined Modality Therapy Epidermal Growth Factor - metabolism ErbB Receptors - metabolism Female Follow-Up Studies Gynecology. Andrology. Obstetrics Humans Mammary gland diseases Medical sciences Middle Aged Prognosis Prospective Studies Survival Rate Tumors |
title | Lack of prognostic value of epidermal growth factor receptor in a series of 229 T1/T2, N0/N1 breast cancers, with well defined prognostic parameters |
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