<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>RSS for Elevated plasma endoglin (CD105) predicts decreased response and survival in a metastatic breast cancer trial of hormone therapy</title><link>http://journalogy.net/Rss.aspx?cata=9&amp;id=29112378</link><description>Search RSS feed for Microsoft Academic Search</description><generator>MSRA Libra RSS Burner</generator><copyright>(c)2008 Microsoft Corpration, All right reserved.</copyright><pubDate>Thu, 23 May 2013 07:55:35 GMT</pubDate><lastBuildDate>Thu, 23 May 2013 07:55:35 GMT</lastBuildDate><category /><item><title>Elevated plasma endoglin (CD105) predicts decreased response and survival in a metastatic breast cancer trial of hormone therapy</title><link>http://journalogy.net/Publication/29112378</link><pubDate>Thu, 23 May 2013 00:55:35 GMT</pubDate><guid isPermaLink="false">291123783</guid><description><![CDATA[<div><a href="http://journalogy.net/Author/47669300">M. N. Vo</a>, <a href="http://journalogy.net/Author/13231848">M. Evans</a>, <a href="http://journalogy.net/Author/23885689">K. Leitzel</a>, <a href="http://journalogy.net/Author/42510049">S. M. Ali</a>, <a href="http://journalogy.net/Author/55319860">M. Wilson</a>, <a href="http://journalogy.net/Author/23633931">L. Demers</a>, <a href="http://journalogy.net/Author/53727649">D. B. Evans</a>, <a href="http://journalogy.net/Author/23448224">A. Lipton</a>:
            
            <span style="margin-left:20px">(Citations:3)</span><span style="margin-left:20px"><a href="http://www.springerlink.com/index/343283r840683637.pdf">view publication</a></span></div><div>Background Endoglin (CD105) is a co-receptor for TGF-β, is expressed by human <a href='http://academic.research.microsoft.com/Keyword/72883/vascular-endothelial'>vascular endothelial</a>  cells, and plays a major role in angiogenesis. Materials and methods Pretreatment EDTA plasma from 224 <a href='http://academic.research.microsoft.com/Keyword/25076/metastatic-breast-cancer'>metastatic breast cancer</a>  patients enrolled in a phase III 2nd-line <a href='http://academic.research.microsoft.com/Keyword/18444/hormone-therapy'>hormone therapy</a>  trial and 50 <a href='http://academic.research.microsoft.com/Keyword/50709/control-subjects'>control subjects</a>  were assayed for endoglin using an ELISA. Results The female <a href='http://academic.research.microsoft.com/Keyword/49663/control-group'>control group</a>  (n = 50) plasma endoglin <a href='http://academic.research.microsoft.com/Keyword/72353/upper-limit-of-normal'>upper limit of normal</a>  was defined as the mean + 2 SD (8.7 ng/ml). The <a href='http://academic.research.microsoft.com/Keyword/47859/breast-cancer'>breast cancer</a>  patient plasma endoglin was 6.40 ± 2.23 ng/ml (range 3.00–19.79 ng/ml). Elevated plasma endoglin levels were detected in 26 of 224 patients (11.6%). Patients with elevated plasma endoglin had a reduced clinical benefit rate (CR + PR + Stable) (15 vs. 42%) (P = 0.01) to hormone therapy. TTP was shorter for patients with elevated plasma endoglin, but did not reach <a href='http://academic.research.microsoft.com/Keyword/39876/statistical-significance'>statistical significance</a>  (P = 0.2). Patients with elevated plasma endoglin had decreased <a href='http://academic.research.microsoft.com/Keyword/29749/overall-survival'>overall survival</a>  (median 645 vs. 947 days) (P = 0.005). Conclusion Elevated pretreatment plasma endoglin levels predicted for decreased clinical benefit and a shorter <a href='http://academic.research.microsoft.com/Keyword/29749/overall-survival'>overall survival</a>  in <a href='http://academic.research.microsoft.com/Keyword/25076/metastatic-breast-cancer'>metastatic breast cancer</a>  patients treated with 2nd-line hormone therapy.</div><div></div><div>Journal: <a href="http://journalogy.net/Journal/2742">Breast Cancer Research and Treatment - BREAST CANCER RES TREAT</a>, vol. 119, no. 3, pp. 767-771, 2010</div><div />]]></description></item></channel></rss>