<?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>15</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Human Recombinant Endostatin Combined with Cisplatin Based Doublets in Treating Patients with Advanced NSCLC and Evaluation by CT Perfusion Imaging</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>6765</FirstPage>
			<LastPage>6768</LastPage>
			<ELocationID EIdType="pii">31493</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>Aims: To study the effectiveness of human recombinant endostatin injection (Endostar®) combined withcisplatin doublets in treating advanced non-small cell lung cancer (NSCLC), and to evaluate outcome by CTperfusion imaging. &lt;br/&gt;&lt;b&gt;Methods&lt;/b&gt;: From April 2011 to September 2014, 76 patients with advanced NSCLC whowere treated with platinum-based doublets were divided into group A (36 patients) and group B (40 patients).Endostar® 15mg/day was administered 4 days before chemotherapy and combined with chemotherapy from day5 in group A, and combined with chemotherapy from the first day in Group B. Endostar® in the two groups wasinjected intravenously for 14 days. &lt;br/&gt;&lt;b&gt;Results&lt;/b&gt;: Treatment effectiveness in the two groups differed with statisticalsignificance (p&lt;0.05). Effectiveness evaluated by CT perfusion imaging, BF, BV, MTT and PS also demonstratedsignificant differences (all p&lt;0.05). Adverse reactions in the two groups did not significantly vary (p&gt; 0.05).&lt;br/&gt;&lt;b&gt;Conclusions&lt;/b&gt;: The response rate with Endostar® administered 4 days before chemotherapy and combined withchemotherapy from day 5 in group A was better than Endostar® combined with chemotherapy from the firstday, and CT perfusion imaging could be a reasonable method for evaluation of patient outcomes.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Advanced NSCLC</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">platinum containing chemotherapy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">CT perfusion imaging</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_31493_d67cac1e94d99f984f5f89568b26e199.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
