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<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>24</Volume>
				<Issue>8</Issue>
				<PubDate PubStatus="epublish">
					<Year>2023</Year>
					<Month>08</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Pretreatment Microvessel Density for Predicting of Tumor Responsiveness to Neoadjuvant Chemoradiotherapy of Locally Advanced Rectal Cancer</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>2697</FirstPage>
			<LastPage>2703</LastPage>
			<ELocationID EIdType="pii">90755</ELocationID>
			
<ELocationID EIdType="doi">10.31557/APJCP.2023.24.8.2697</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Chinakrit </FirstName>
					<LastName>Boonya-Ussadorn</LastName>
<Affiliation>Department of Surgery, Phramongkutklao Hospital, Thailand.</Affiliation>
<Identifier Source="ORCID">0000000247595916</Identifier>

</Author>
<Author>
					<FirstName>Thirayost </FirstName>
					<LastName>Nimmanon</LastName>
<Affiliation>Department of Pathology, Phramongkutklao College of Medicine, Thailand.</Affiliation>
<Identifier Source="ORCID">0000000187651268</Identifier>

</Author>
<Author>
					<FirstName>Sahaphol </FirstName>
					<LastName>Anannamcharoen</LastName>
<Affiliation>Department of Surgery, Phramongkutklao Hospital, Thailand.</Affiliation>
<Identifier Source="ORCID">000000030274564X</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>03</Month>
					<Day>24</Day>
				</PubDate>
			</History>
		<Abstract>Objective: This study aimed to assess whether pretreatment tumor tissue microvessel density (MVD) could be a potential predictive marker for Mandard response in LARC treated with nCRT. Methods: A retrospective analysis was performed in pretreatment paraffin-embedded specimens of 31 pathologically confirmed rectal adenocarcinoma. All patients received nCRT and subsequent total mesorectal resection. Tumor MVD was determined by an average number of counted CD34-stained endothelial cells from two selected fields at 200x magnification in each slide and categorized into two groups: low MVD (&lt;/=60) and high MVD (&gt; 60). The tumor response was determined using the Mandard tumor regression grading system. The subjects were grouped according to their TRG into responder (TRG 1-3) and non-responder (TRG 4–5). Result: Twenty out of thirty-one patients (64.5%) were defined as responders. Eleven patients (35.5%) were defined as non-responders. MVD was significantly associated with tumor responsiveness to nCRT (p &lt; 0.05). High MVD was shown to be an independent risk factor associated with tumor resistance to nCRT (OR, 22.58; 95% CI, 1.943-262.34; p = 0.013). A strong correlation was found between MVD and TRG (correlation coefficient value of 0.642, p &lt;0.01), between MVD and vascular invasion (correlation coefficient value of 0.618, p &lt;0.01), and between nodal involvement and vascular invasion (correlation coefficient value of 0.521, p &lt;0.01). A moderate correlation was found between nodal involvement and vascular invasion (correlation coefficient value of 0.406, p &lt;0.05). Conclusion: High MVD in pretreatment tumor tissue was significantly associated with the tumor resistance to nCRT.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">microvessel density</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Tumor regression. Rectal cancer</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">radiotherapy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Mandard</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_90755_1d347663cbd39dbd18a117221dac8a59.pdf</ArchiveCopySource>
</Article>
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