<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>2</title>
<title_fa>1</title_fa>
<short_title>3</short_title>
<subject>Literature &amp; Humanities</subject>
<web_url>http://idai.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>9</journal_id_issn>
<journal_id_issn_online>10</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>7</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1390</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2012</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>3</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>The role of 18F-FDG PET/CT metabolic tumour volume in predicting survival in patients with metastatic nasopharyngeal carcinoma</title>
	<subject_fa>بیماری های دهان</subject_fa>
	<subject>Oral Medicine</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt; &lt;strong&gt;Objectives&lt;/strong&gt; To investigate the role of PET-derived imaging markers in predicting metastatic nasopharyngeal carcinoma (NPC) outcomes. &lt;strong&gt;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt; &lt;strong&gt;Materials and methods&lt;/strong&gt; A total of 56 patients with metastatic NPC were enrolled. Before treatment, all of the participants underwent 18F-FDG PET/CT. The following 18F-FDG PET parameters were assessed: standardised uptake value, metabolic tumour volume (MTV), and total lesion glycolysis. Multivariate Cox proportional hazards models were used to identify the independent predictors of survival. &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Results&lt;/strong&gt; The multivariate analysis showed that performance status&gt;1 (P=0.007), Epstein–Barr virus (EBV) DNA titre&gt;5000copies/mL (P=0.001), and MTV&gt;110mL (P=0.013) were independent risk factors for progression-free survival (PFS). Male sex (P=0.004), performance status&gt;1 (P&lt;0.0001), EBV DNA level&gt;5000copies/mL (P&lt;0.0001), and MTV&gt;110mL (P=0.003) independently predicted overall survival (OS). The 2-year PFS and OS rates of the patients with MTV⩽110mL were 23.2% and 43%, respectively, compared with 0% and 9.1%, respectively, for those with MTV&gt;110mL. Combining the MTV with the EBV DNA titre allowed further survival stratification by dividing the patients into three groups with distinct PFS (2-year rates=30.8%, 7.1%, and 0%, P&lt;0.0001) and OS (2-year rates=68.4%, 40%, and 0%, P&lt;0.0001) rates. &lt;/p&gt;&lt;p&gt; &lt;strong&gt;Conclusion&lt;/strong&gt; The MTV appears to be an independent risk factor in metastatic NPC patients. This factor is complementary to the EBV DNA titre for predicting survival in metastatic NPC. &lt;/p&gt;&lt;hr&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt; &lt;strong&gt;Source: &lt;/strong&gt;Journal of Oral Oncology &lt;/p&gt;&lt;p&gt; &lt;a href=&quot;http://www.oraloncology.com/article/S1368-8375(12)00244-8/abstract&quot; target=&quot;_blank&quot;&gt;&lt;font color=&quot;#0033ff&quot;&gt;Full Text&lt;/font&gt;&lt;/a&gt; &lt;/p&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Metabolic tumour volume, Total lesion glycolysis, Standardised uptake value, Metastasis, Nasopharyngeal carcinoma, 18F-FDG PET/CT, Epstein–Barr virus, Prognosis, Head and neck cancer</keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://idai.ir/browse.php?a_code=A-10-32-859&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Sheng-Chieh</first_name>
	<middle_name></middle_name>
	<last_name> Chan</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003750</code>
	<orcid>10031947532846003750</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Nuclear Medicine, Chang Gung Memorial Hospital, Keelong, Taiwan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Cheng-Lung</first_name>
	<middle_name></middle_name>
	<last_name> Hsu</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003751</code>
	<orcid>10031947532846003751</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Division of Haematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name> Tzu-Chen</first_name>
	<middle_name></middle_name>
	<last_name>Yen</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003752</code>
	<orcid>10031947532846003752</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Nuclear Medicine and Molecular Imaging Center, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Shu-Hang</first_name>
	<middle_name></middle_name>
	<last_name>Ng</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003753</code>
	<orcid>10031947532846003753</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Diagnostic Radiology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Chun-Ta</first_name>
	<middle_name></middle_name>
	<last_name>Liao</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003754</code>
	<orcid>10031947532846003754</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Otorhinolaryngology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Hung-Ming</first_name>
	<middle_name></middle_name>
	<last_name>Wang</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846003755</code>
	<orcid>10031947532846003755</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Division of Haematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
