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	<title>Comments on: Immunopheotype of Gastrointestinal stromal tumours (GIST)</title>
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	<link>http://pathtalk.org/archives/1196</link>
	<description>is a weblog about pathology and laboratory medicine.</description>
	<lastBuildDate>Tue, 24 Apr 2012 10:23:45 +0000</lastBuildDate>
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		<title>By: PathDoc15</title>
		<link>http://pathtalk.org/archives/1196/comment-page-1#comment-1199</link>
		<dc:creator>PathDoc15</dc:creator>
		<pubDate>Mon, 13 Jul 2009 12:32:14 +0000</pubDate>
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		<description>Excellent summary - It is interesting that in other tumor types (melanoma for example), CKIT IHC is a very poor surogate for mutation status of CKIT.  Is it a perfect corelate in GIST?

I remember a recent trial showing that patients with GISTs that harbor specific mutations in CKIT (I can&#039;t remember which) responded better to imatinib dose escallation.  Is there a role for mutation analysis in the management of GIST?

Thanks for the post!</description>
		<content:encoded><![CDATA[<p>Excellent summary &#8211; It is interesting that in other tumor types (melanoma for example), CKIT IHC is a very poor surogate for mutation status of CKIT.  Is it a perfect corelate in GIST?</p>
<p>I remember a recent trial showing that patients with GISTs that harbor specific mutations in CKIT (I can&#8217;t remember which) responded better to imatinib dose escallation.  Is there a role for mutation analysis in the management of GIST?</p>
<p>Thanks for the post!</p>
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	<item>
		<title>By: P.Das</title>
		<link>http://pathtalk.org/archives/1196/comment-page-1#comment-1192</link>
		<dc:creator>P.Das</dc:creator>
		<pubDate>Thu, 09 Jul 2009 02:58:56 +0000</pubDate>
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		<description>Excellent post.Thanks</description>
		<content:encoded><![CDATA[<p>Excellent post.Thanks</p>
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