<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName>West Asia Organization for Cancer Prevention (WAOCP), APOCP's West Asia Chapter.</PublisherName>
				<JournalTitle>Asian Pacific Journal of Cancer Prevention</JournalTitle>
				<Issn>1513-7368</Issn>
				<Volume>16</Volume>
				<Issue>5</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>05</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Efficacy and Toxicity of Sunitinib in Metastatic Renal Cell Carcinoma Patients in Egypt</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1971</FirstPage>
			<LastPage>1976</LastPage>
			<ELocationID EIdType="pii">30692</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>1970</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</History>
		<Abstract>&lt;b&gt;Background:&lt;/b&gt; To evaluate our results in terms of response, survival and toxicity profile of sunitinib amongEgyptian patients with metastatic renal cell carcinoma. Materials and &lt;br/&gt;&lt;b&gt;Methods&lt;/b&gt;: Between January 2010 andDecember 2013, 44 patients with metastatic renal cell carcinoma who received sunitinib at an oncology centerof Cairo university hospitals were enrolled in this retrospective analysis. &lt;br/&gt;&lt;b&gt;Results&lt;/b&gt;: The median age of the patientswas 53 years, 22 (50%) having localized disease at presentation ,while the remaining half of the patients presentedwith metastasis. At a median follow up of 19 months, 9 (21%) patients achieved partial remission, while diseasewas reported stable in 20 cases (45%) and progressive in 7 (16%), 4 (9%) being lost to follow up, and 4 (9%)had discontinued therapy due to toxicity. The median overall survival was 23 months (95%CI 15.2 - 30.9), whileprogression free survival was 12 months (95%CI 11.6 - 12.3). The most commonly reported non hematologicalgrade 3 adverse events included mucositis (15.9%), hand-foot syndrome (13.6%), and fatigue (9%), while thepredominant grade 3 or 4 laboratory abnormalities were neutropenia (6.8%), followed by anemia in 4.5% ofpatients. &lt;br/&gt;&lt;b&gt;Conclusions&lt;/b&gt;: Our efficacy data were comparable to the published literature in terms of progressionfree survival and overall survival , while toxicity profile is different from Asian and western countries. However,sunitinib adverse events were manageable and tolerable in most of our Egyptian patients</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">renal cell carcinoma</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">sunitinib</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Toxicity</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Efficacy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Egyptian cases</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_30692_f31bc5c15a648141834c33392eaa29a3.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
