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<pubDate>Sat, 19 Jul 2008 04:40:43 BST</pubDate>


	<title>CiteULike: omalbam's cancer</title>
	<description>CiteULike: omalbam's cancer</description>


	<link>http://www.citeulike.org/user/omalbam/tag/cancer</link>
	<dc:publisher>CiteULike.org</dc:publisher>
	<dc:language>en-gb</dc:language>
	<dc:rights>Copyright &#169; 2004-2008 citeulike.org</dc:rights>
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        <rdf:li rdf:resource="http://www.citeulike.org/user/omalbam/article/599311"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/omalbam/article/2112629"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/omalbam/article/2216540"/>

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<item rdf:about="http://www.citeulike.org/user/omalbam/article/599311">
    <title>New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada.</title>
    <link>http://www.citeulike.org/user/omalbam/article/599311</link>
    <description>&lt;i&gt;J Natl Cancer Inst, Vol. 92, No. 3. (2 February 2000), pp. 205-216.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Anticancer cytotoxic agents go through a process by which their antitumor activity-on the basis of the amount of tumor shrinkage they could generate-has been investigated. In the late 1970s, the International Union Against Cancer and the World Health Organization introduced specific criteria for the codification of tumor response evaluation. In 1994, several organizations involved in clinical research combined forces to tackle the review of these criteria on the basis of the experience and knowledge acquired since then. After several years of intensive discussions, a new set of guidelines is ready that will supersede the former criteria. In parallel to this initiative, one of the participating groups developed a model by which response rates could be derived from unidimensional measurement of tumor lesions instead of the usual bidimensional approach. This new concept has been largely validated by the Response Evaluation Criteria in Solid Tumors Group and integrated into the present guidelines. This special article also provides some philosophic background to clarify the various purposes of response evaluation. It proposes a model by which a combined assessment of all existing lesions, characterized by target lesions (to be measured) and nontarget lesions, is used to extrapolate an overall response to treatment. Methods of assessing tumor lesions are better codified, briefly within the guidelines and in more detail in Appendix I. All other aspects of response evaluation have been discussed, reviewed, and amended whenever appropriate.</description>
    <dc:title>New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada.</dc:title>

    <dc:creator>P Therasse</dc:creator>
    <dc:creator>SG Arbuck</dc:creator>
    <dc:creator>EA Eisenhauer</dc:creator>
    <dc:creator>J Wanders</dc:creator>
    <dc:creator>RS Kaplan</dc:creator>
    <dc:creator>L Rubinstein</dc:creator>
    <dc:creator>J Verweij</dc:creator>
    <dc:creator>M Van Glabbeke</dc:creator>
    <dc:creator>AT van Oosterom</dc:creator>
    <dc:creator>MC Christian</dc:creator>
    <dc:creator>SG Gwyther</dc:creator>
    <dc:identifier>doi:10.1093/jnci/92.3.205</dc:identifier>
    <dc:source>J Natl Cancer Inst, Vol. 92, No. 3. (2 February 2000), pp. 205-216.</dc:source>
    <dc:date>2006-04-25T07:20:03-00:00</dc:date>
    <prism:publicationYear>2000</prism:publicationYear>
    <prism:publicationName>J Natl Cancer Inst</prism:publicationName>
    <prism:issn>0027-8874</prism:issn>
    <prism:volume>92</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>205</prism:startingPage>
    <prism:endingPage>216</prism:endingPage>
    <prism:category>cancer</prism:category>
    <prism:category>diagnosis</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/omalbam/article/2112629">
    <title>Anti-androgens increase N-terminal pro-BNP levels in men with prostate cancer</title>
    <link>http://www.citeulike.org/user/omalbam/article/2112629</link>
    <description>&lt;i&gt;Clinical Endocrinology, Vol. 68, No. 1. (January 2008), pp. 59-65.&lt;/i&gt;</description>
    <dc:title>Anti-androgens increase N-terminal pro-BNP levels in men with prostate cancer</dc:title>

    <dc:creator>Dockery</dc:creator>
    <dc:creator>Frances</dc:creator>
    <dc:creator>Bulpitt</dc:creator>
    <dc:creator>J Christopher</dc:creator>
    <dc:creator>Agarwal</dc:creator>
    <dc:creator>Sanjiv</dc:creator>
    <dc:creator>Vernon</dc:creator>
    <dc:creator>Clare</dc:creator>
    <dc:creator>Nihoyannopoulos</dc:creator>
    <dc:creator>Petros</dc:creator>
    <dc:creator>Kemp</dc:creator>
    <dc:creator>Martin</dc:creator>
    <dc:creator>Hooper</dc:creator>
    <dc:creator>James</dc:creator>
    <dc:creator>Rajkumar</dc:creator>
    <dc:creator>Chakravarthi</dc:creator>
    <dc:identifier>doi:10.1111/j.1365-2265.2007.02999.x</dc:identifier>
    <dc:source>Clinical Endocrinology, Vol. 68, No. 1. (January 2008), pp. 59-65.</dc:source>
    <dc:date>2007-12-14T09:35:43-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Clinical Endocrinology</prism:publicationName>
    <prism:issn>0300-0664</prism:issn>
    <prism:volume>68</prism:volume>
    <prism:number>1</prism:number>
    <prism:startingPage>59</prism:startingPage>
    <prism:endingPage>65</prism:endingPage>
    <prism:publisher>Blackwell Publishing</prism:publisher>
    <prism:category>androgen</prism:category>
    <prism:category>cancer</prism:category>
    <prism:category>cardiovascular</prism:category>
    <prism:category>therapy</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/omalbam/article/2216540">
    <title>Approach to the Prostate Cancer Patient with Bone Disease</title>
    <link>http://www.citeulike.org/user/omalbam/article/2216540</link>
    <description>&lt;i&gt;J Clin Endocrinol Metab, Vol. 93, No. 1. (1 January 2008), pp. 2-7.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Prostate cancer is the most common visceral malignancy in men. Androgen deprivation therapy (ADT) is commonly used in patients with nonmetastatic prostate cancer and is associated with significant bone loss and fractures. The greatest bone loss occurs during initiation of ADT. Men should have assessment of skeletal integrity with bone mineral density examination by dual x-ray absorptiometry of the hip and spine. Men with fragility fractures or osteoporosis by bone density should be considered for bisphosphonate therapy. Men with low bone mass may need antiresorptive therapy, depending on other risk factors. Men with a normal bone mineral density should be followed up closely with bone densitometry while on ADT. All men should receive preventive measures with calcium (1200 mg daily in divided doses), vitamin D (8001000 IU/d), and weight-bearing exercise. Men should be evaluated for additional secondary causes of bone loss including vitamin D insufficiency. Guidelines are needed for androgen-induced bone loss screening and treatment. 10.1210/jc.2007-1402</description>
    <dc:title>Approach to the Prostate Cancer Patient with Bone Disease</dc:title>

    <dc:creator>Susan Greenspan</dc:creator>
    <dc:identifier>doi:10.1210/jc.2007-1402</dc:identifier>
    <dc:source>J Clin Endocrinol Metab, Vol. 93, No. 1. (1 January 2008), pp. 2-7.</dc:source>
    <dc:date>2008-01-10T22:51:41-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>J Clin Endocrinol Metab</prism:publicationName>
    <prism:volume>93</prism:volume>
    <prism:number>1</prism:number>
    <prism:startingPage>2</prism:startingPage>
    <prism:endingPage>7</prism:endingPage>
    <prism:category>cancer</prism:category>
    <prism:category>osteoporosis</prism:category>
    <prism:category>sideffects</prism:category>
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