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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>22</Volume>
				<Issue>10</Issue>
				<PubDate PubStatus="epublish">
					<Year>2021</Year>
					<Month>10</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Serum Biomarkers for Chemotherapy Cardiotoxicity Risk Detection of Breast Cancer Patients</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>3355</FirstPage>
			<LastPage>3363</LastPage>
			<ELocationID EIdType="pii">89812</ELocationID>
			
<ELocationID EIdType="doi">10.31557/APJCP.2021.22.10.3355</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Diya </FirstName>
					<LastName>Hasan</LastName>
<Affiliation>Al-Balqa Applied University, Zarqa College, Department of Allied Medical Sciences, Zarqa, Jordan.</Affiliation>

</Author>
<Author>
					<FirstName>Yazan </FirstName>
					<LastName>Ismail</LastName>
<Affiliation>Higher Colleges of
Technology, Faculty of Health Sciences, Abu Dhabi, United Arab Emirates.</Affiliation>

</Author>
<Author>
					<FirstName>Ahmad </FirstName>
					<LastName>Al Tibi</LastName>
<Affiliation>Biolab Diagnostic Laboratories, Amman, Jordan.</Affiliation>

</Author>
<Author>
					<FirstName>Safaa A</FirstName>
					<LastName>AL-Zeidaneen</LastName>
<Affiliation>Al-Balqa Applied University, Zarqa College, Department of Allied Medical Sciences, Zarqa, Jordan.</Affiliation>

</Author>
<Author>
					<FirstName>Mohanad </FirstName>
					<LastName>Odeh</LastName>
<Affiliation>Hashemite University, Faculty of Pharmaceutical Sciences, Department of Clinical Pharmacy and Pharmacy Practice,
Zarqa, Jordan.</Affiliation>

</Author>
<Author>
					<FirstName>George J </FirstName>
					<LastName>Burghel</LastName>
<Affiliation>Manchester University NHS Foundation Trust, Manchester Centre for Genomics Medicine, Manchester, UK.</Affiliation>

</Author>
<Author>
					<FirstName>Iyad </FirstName>
					<LastName>Natsheh</LastName>
<Affiliation>Al-Balqa Applied University, Zarqa College, Department of Allied Medical Sciences, Zarqa, Jordan.</Affiliation>

</Author>
<Author>
					<FirstName>Amid </FirstName>
					<LastName>Abdelnour</LastName>
<Affiliation>Biolab Diagnostic Laboratories, Amman, Jordan.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2021</Year>
					<Month>04</Month>
					<Day>27</Day>
				</PubDate>
			</History>
		<Abstract>Objective: This study aimed to investigate level fluctuations of serum biomarkers that are associated with cardiotoxicity risk, such as high-sensitivity C-reactive protein (hs-CRP) and apolipoprotein-B (Apo-B) in response to chemotherapy treatment for breast cancer. Method: The serum levels of hs-CRP and Apo-B were evaluated in 56 breast cancer patients with main inclusion criteria: HER2 negative and who received adjuvant chemotherapy AC [A: Adriamycin, C: Cyclophosphamide] or AC→T [A: Adriamycin, C: Cyclophosphamide, T: Taxane] regimes at early II (n = 26) and late IV (n = 30) clinical stages by using particle enhanced turbidimetric assay. Results: The results of this study suggest that a high level of pre-treatment hs-CRP is a good prognostic marker in comparison to Apo-B. Moreover, the AC-T chemotherapy regime treatment in both early and late stages exhibited a significantly higher level of hs-CRP compared to that in the AC regime. Hs-CRP was significantly elevated in the early stage in comparison to the late stage among cancer patients, meanwhile Apo-B behaved inversely. Furthermore, the results showed that hs-CRP levels were significantly higher in late-stage cancer patients compared with those in early-stage in both chemotherapy regimens groups. On the other hand, Apo-B showed no significant differences. Conclusion: Monitoring hs-CRP level changes in comparison to Apo-B can be used to assist the side effect risk difference among different chemotherapy regimens, and staging reflecting a positive correlation between them more notable in the late stage.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Hs-CRP</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apo-B</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Chemotherapy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cardiotoxicity</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">breast cancer</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_89812_4cf105bbebe1a0809dbbb7b9b72cb151.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
