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        <title>Head &amp; Neck Oncology - Most accessed articles</title>
        <link>http://www.headandneckoncology.org</link>
        <description>The most accessed research articles published by Head &amp; Neck Oncology</description>
        <dc:date>2012-05-04T00:00:00Z</dc:date>
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        <title>The cost burden of oral, oral pharyngeal, and salivary gland cancers in three groups: commercial insurance, medicare, and medicaid</title>
        <description>Background:
Head and neck cancers are of particular interest to health care providers, their patients, and those paying for health care services, because they have a high morbidity, they are extremely expensive to treat, and of the survivors only 48% return to work. Consequently the economic burden of oral cavity, oral pharyngeal, and salivary gland cancer (OC/OP/SG) must be understood. The cost of these cancers in the U.S. has not been investigated.
Methods:
A retrospective analysis of administrative claims data for 6,812 OC/OP/SG cancer patients was undertaken. Total annual health care spending for OC/OP/SG cancer patients was compared to similar patients without OC/OP/SG cancer using propensity score matching for enrollees in commercial insurance, Medicare, and Medicaid. Indirect costs, as measured by short term disability days were compared for employed patients.
Results:
Total annual health care spending for OC/OP/SG patients during the year after the index diagnosis was $79,151 for the Commercial population. Health care costs were higher for OC/OP/SG cancer patients with Commercial Insurance ($71,732, n = 3,918), Medicare ($35,890, n = 2,303) and Medicaid ($44,541, n = 585) than the comparison group (all p &lt; 0.01). Commercially-insured employees with cancer (n = 281) had 44.9 more short-term disability days than comparison employees (p &lt; 0.01). Multimodality treatment was twice the cost of single modality therapy. Those patients receiving all three treatments (surgery, radiation, and chemotherapy) had the highest costs of cost of care, from $96,520 in the Medicare population to $153,892 in the Commercial population.
Conclusions:
In the U.S., the cost of OC/OP/SG cancer is significant and may be the most costly cancer to treat in the U.S. The results of this analysis provide useful information to health care providers and decision makers in understanding the economic burden of head and neck cancer. Additionally, this cost information will greatly assist in determining the cost-effectiveness of new technologies and early detection systems. Earlier identification of cancers by patients and providers may potentially decrease health care costs, morbidity and mortality.</description>
        <link>http://www.headandneckoncology.org/content/4/1/15</link>
                <dc:creator>Jed Jacobson</dc:creator>
                <dc:creator>Joel Epstein</dc:creator>
                <dc:creator>Frederick Eichmiller</dc:creator>
                <dc:creator>Teresa Gibson</dc:creator>
                <dc:creator>Ginger Carls</dc:creator>
                <dc:creator>Emily Vogtmann</dc:creator>
                <dc:creator>Shaohung Wang</dc:creator>
                <dc:creator>Barbara Murphy</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2012, null:15</dc:source>
        <dc:date>2012-04-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-4-15</dc:identifier>
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        <item rdf:about="http://www.headandneckoncology.org/content/1/1/36">
        <title>HPV &amp; head and neck cancer: a descriptive update</title>
        <description>The incidence of head and neck squamous cell carcinoma (HNSCC) has been gradually increasing over the last three decades. Recent data have now attributed a viral aetiology to a subset of head and neck cancers. Several studies indicate that oral human papillomavirus (HPV) infection is likely to be sexually acquired. The dominance of HPV 16 in HPV+ HNSCC is even greater than that seen in cervical carcinoma of total worldwide cases. Strong evidence suggests that HPV+ status is an important prognostic factor associated with a favourable outcome in head and neck cancers.Approximately 30 to 40% of HNSCC patients with present with early stage I/II disease. These patients are treated with curative intent using single modality treatments either radiation or surgery alone. A non-operative approach is favored for patients in which surgery followed by either radiation alone or radiochemotherapy may lead to severe functional impairment. Cetuximab, a humanized mouse anti-EGFR IgG1 monoclonal antibody, improved locoregional control and overall survival in combination with radiotherapy in locally advanced tumours but at the cost of some increased cardiac morbidity and mortality.Finally, the improved prognosis and treatment responses to chemotherapy and radiotherapy by HPV+ tumours may suggest that HPV status detection is required to better plan and individualize patient treatment regimes.</description>
        <link>http://www.headandneckoncology.org/content/1/1/36</link>
                <dc:creator>Peter Goon</dc:creator>
                <dc:creator>Margaret Stanley</dc:creator>
                <dc:creator>Jorg Ebmeyer</dc:creator>
                <dc:creator>Lars Steinstraesser</dc:creator>
                <dc:creator>Tahwinder Upile</dc:creator>
                <dc:creator>Waseem Jerjes</dc:creator>
                <dc:creator>Manuel Bernal-Sprekelsen</dc:creator>
                <dc:creator>Martin Gorner</dc:creator>
                <dc:creator>Holger Sudhoff</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2009, null:36</dc:source>
        <dc:date>2009-10-14T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-1-36</dc:identifier>
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        <item rdf:about="http://www.headandneckoncology.org/content/3/1/2">
        <title>Oral squamous cell cancer: Early detection and the role of alcohol and smoking.</title>
        <description>ObjectiveOral squamous cell carcinoma has a remarkable incidence worldwide and a fairly onerous prognosis, encouraging further research on factors that might modify disease outcome.Data sourcesA web-based search for all types of articles published was initiated using Medline/Pub Med, with the key words such as oral cancer, alcohol consumption, genetic polymorphisms, tobacco smoking and prevention. The search was restricted to articles published in English, with no publication date restriction (last update 2010).Review MethodsIn this review article, we approach the factors for a cytologic diagnosis during OSCC development and the markers used in modern diagnostic technologies as well. We also reviewed available studies of the combined effects of alcohol drinking and genetic polymorphisms on alcohol-related cancer risk.
Results:
The interaction of smoking and alcohol significantly increases the risk for aero-digestive cancers. The interaction between smoking and alcohol consumption seems to be responsible for a significant amount of disease.
Conclusion:
Published scientific data show promising pathways for the future development of more effective prognosis. There is a clear need for new prognostic indicators, which could be used in diagnostics and, therefore a better selection of the most effective treatment can be achieved.</description>
        <link>http://www.headandneckoncology.org/content/3/1/2</link>
                <dc:creator>Anna Zygogianni</dc:creator>
                <dc:creator>George Kyrgias</dc:creator>
                <dc:creator>Petros Karakitsos</dc:creator>
                <dc:creator>Amanta Psyrri</dc:creator>
                <dc:creator>John Kouvaris</dc:creator>
                <dc:creator>Nikolaos Kelekis</dc:creator>
                <dc:creator>Vassilios Kouloulias</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2011, null:2</dc:source>
        <dc:date>2011-01-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-3-2</dc:identifier>
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        <item rdf:about="http://www.headandneckoncology.org/content/2/1/11">
        <title>Management of Thyroid nodules in adult patients</title>
        <description>Thyroid nodule is a common presentation and requires a structured diagnostic approach to ascertain the risk of malignancy and determine appropriate management. This review article highlights the key points in the history and examination which can help with risk stratification. It also discussed the application of fine needle aspiration cytology findings and the British Thyroid Association Guidelines in clinical practice.</description>
        <link>http://www.headandneckoncology.org/content/2/1/11</link>
                <dc:creator>Chee Yean Eng</dc:creator>
                <dc:creator>Muhammad Quraishi</dc:creator>
                <dc:creator>Patrick Bradley</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2010, null:11</dc:source>
        <dc:date>2010-05-05T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-2-11</dc:identifier>
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        <item rdf:about="http://www.headandneckoncology.org/content/4/1/5">
        <title>cTNM vs. pTNM: the effect of not applying ultrasonography in the identification of cervical nodal disease</title>
        <description>Accurate clinical staging of oral squamous cell cancer can be quite difficult to achieve especially if nodal involvement is identified. Radiologically-assisted clinical staging is more accurate and informs the clinician of loco-regional and distant metastasis.In this study, we compared clinical TNM (cTNM) staging (not including ultrasonography) to pathological TNM (pTNM) staging in 245 patients presenting with carcinoma of the oral cavity and the oro-pharyngeal region. Tumour size differences and nodal involvement were highlighted. US reports of the neck were then added to the clinical staging and results compared.Tumour size was clinically underestimated in 4 T1, 2 T2 and 2 T3 oral diseases. Also 20 patients that were reported as nodal disease free had histological proven N1 or N2 nodal involvement; while 3 patients with cTNM showing N1 disease had histologically proven N2 disease.Overall the agreement between the 2 systems per 1 site was 86.6% (Kappa agreement = 0.80), per 2 sites 90.0% (Kappa agreement = 0.68) and per 3 sites 90.5% (Kappa agreement 0.62).An accurate clinical staging is of an utmost importance. It is the corner stone in which the surgical team build the surgical treatment plan and decide whether an adjuvant therapy is required to deal with any possible problem that might arise. The failure to achieve an accurate staging may lead to incomplete surgical planning and hence unforeseen problems that may adversely affect the patient&apos;s survival.</description>
        <link>http://www.headandneckoncology.org/content/4/1/5</link>
                <dc:creator>Waseem Jerjes</dc:creator>
                <dc:creator>Tahwinder Upile</dc:creator>
                <dc:creator>Hani Radhi</dc:creator>
                <dc:creator>Aviva Petrie</dc:creator>
                <dc:creator>Jesuloba Abiola</dc:creator>
                <dc:creator>Aidan Adams</dc:creator>
                <dc:creator>Jacqueline Callear</dc:creator>
                <dc:creator>Panagiotis Kafas</dc:creator>
                <dc:creator>Syedda Abbas</dc:creator>
                <dc:creator>Kartic Rajaram</dc:creator>
                <dc:creator>Colin Hopper</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2012, null:5</dc:source>
        <dc:date>2012-03-12T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-4-5</dc:identifier>
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        <prism:startingPage>5</prism:startingPage>
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        <item rdf:about="http://www.headandneckoncology.org/content/1/1/35">
        <title>Prevention of complications in neck dissection</title>
        <description>Background:
The neck dissection has remained a pivotal aspect of head and neck cancer management for over a century. During this time its role has expanded from a purely therapeutic option into an elective setting, in part promoted by efforts to reduce its morbidity.ObjectivesThis review will consider the potential complications of neck dissection and on the basis of the available evidence describe both their management and prevention.
Conclusion:
Although the neck dissection continues to provide clinicians with a method of addressing cervical disease, its reliability and safety can only be assured if surgeons remain cognisant of the potential complications and aim to minimise such morbidity by appropriate management in the peri-operative period.</description>
        <link>http://www.headandneckoncology.org/content/1/1/35</link>
                <dc:creator>Cyrus Kerawala</dc:creator>
                <dc:creator>Manolis Heliotis</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2009, null:35</dc:source>
        <dc:date>2009-10-12T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-1-35</dc:identifier>
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        <prism:startingPage>35</prism:startingPage>
        <prism:publicationDate>2009-10-12T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.headandneckoncology.org/content/2/1/1">
        <title>Unicystic ameloblastoma of the mandible - an unusual case report and review of literature</title>
        <description>Ameloblastoma is a true neoplasm of odontogenic epithelial origin. It is the second most common odontogenic neoplasm, and only odontoma outnumbers it in reported frequency of occurrence. Its incidence, combined with its clinical behavior, makes ameloblastoma the most significant odontogenic neoplasm. Unicystic ameloblastoma (UA) refers to those cystic lesions that show clinical, radiographic, or gross features of a mandibular cyst, but on histologic examination show a typical ameloblastomatous epithelium lining part of the cyst cavity, with or without luminal and/or mural tumor growth. It accounts for 5-15% of all intraosseous ameloblastomas. We report a case of unicystic ameloblastoma in a 30-year-old female, and review the literature.</description>
        <link>http://www.headandneckoncology.org/content/2/1/1</link>
                <dc:creator>Rakesh Ramesh</dc:creator>
                <dc:creator>Suraj Manjunath</dc:creator>
                <dc:creator>Tanveer Ustad</dc:creator>
                <dc:creator>Saira Pais</dc:creator>
                <dc:creator>Shivakumar K</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2010, null:1</dc:source>
        <dc:date>2010-01-14T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-2-1</dc:identifier>
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                <prism:publicationName>Head &amp; Neck Oncology</prism:publicationName>
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        <prism:startingPage>1</prism:startingPage>
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        <item rdf:about="http://www.headandneckoncology.org/content/4/1/13">
        <title>Clear cell chondrosarcoma of the head and neck</title>
        <description>Clear cell chondrosarcoma is a rare variant of chondrosarcoma that mostly involves the end of long bones. However, nine cases have been reported in the head and neck: four in larynx, two in nasal septum, two in maxilla and one in the skull. These cases form the basis of this review. Head and neck cases accounts for less than 5% of Clear cell chondrosarcomas in the whole body and the larynx is the most common place. The histological findings of head and neck cases are consistent with general features of this entity in the whole body and nearly all tumors in this case series had a component of conventional chondrosarcoma. Clear cell chondrosarcoma is an intracompartmental tumor and retains &quot;Grenz zone&quot; just beneath the epithelium. Therefore, the overlying mucosa remained intact in all laryngeal cases. Nasal tumor caused ballooning of the septum and the maxillary lesion did not involve the oral mucosa. This tumor presents various radiographic features in the head and neck area. Chondroblastoma, chondroma, osteoblastoma, osteosarcoma and metastatic renal cell carcinoma are included in the histologic differential diagnoses. Differentiation from chondroblastic osteosarcoma is important in the maxilla. A wide resection is adequate in most cases. However, some laryngeal cases show tendency to recur. Clear cell chondrosarcoma is a slow growing tumor and this necessitates a long time follow-up of patients. Due to the extreme rarity in the head and neck, diagnosis of Clear cell chondrosarcoma in this area, must be confirmed by histochemical and immunohistochemical studies.</description>
        <link>http://www.headandneckoncology.org/content/4/1/13</link>
                <dc:creator>Sepideh Mokhtari</dc:creator>
                <dc:creator>Abbas Mirafsharieh</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2012, null:13</dc:source>
        <dc:date>2012-04-20T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-4-13</dc:identifier>
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        <item rdf:about="http://www.headandneckoncology.org/content/4/1/11">
        <title>Knockdown of aberrantly expressed nuclear localized decorin attenuates tumour angiogenesis related mediators in oral cancer progression model in vitro</title>
        <description>Background:
Oral cancer accounts for roughly 3% of cancer cases in the world with about 350,000 newly reported cases annually and a 5-year survival rate of only 50%. Majority of oral cancers are squamous cell carcinomas that originate in the oral mucosal epithelial linings. We have previously shown that in human malignant squamous cells carcinoma (SCC-25) as well as in dysplastic oral keratinocytes (DOK), a small leucine-rich multifunctional proteoglycan decorin is aberrantly expressed and localized in the nucleus where it interacts with nuclear epidermal growth factor receptor (EGFR). Post-transcriptional silencing of nuclear decorin significantly reduced IL-8 and IL8-dependent migration and invasion in these dysplastic and malignant oral epithelia. The objective of this study was to further examine the effects of nuclear decorin silencing on angiogenesis and angiogenesis related mediators in this oral cancer progression cell line model.
Methods:
We have used multiplex PCR, western blotting, and in vitro endothelial tube formation assay to study angiogenesis and related pathways in nuclear decorin silenced (stable knockdown) DOK and SCC-25 cells.
Results:
Nuclear decorin knockdown resulted in significant down regulation of IL-8 expression, however IL-10, and TGF-beta expression was not affected in either DOK or SCC25 cells as measured by multiplex RT PCR. IL-8 receptor CXCR 1 and 2 expression was slightly lower in nuclear decorin silenced cells indicating a contributing mechanism in previously shown reduced IL-8 mediated migration and invasion phenotype in these cells. IL-8 is known to induce Matrix metalloproteinase 9 (MMP9) which not only plays a role in tumour migration and invasion but also induces angiogenic switch. We found MMP9 to be significantly reduced in nuclear decorin silenced dysplastic and malignant oral epithelia. Other potent angiogenic mediators, VEGF189 and ANG-1 were either significantly reduced or completely abrogated in these cells. Angiogenesis as measured by endothelial tube-like formations of HUVEC cells was reduced by almost 50 percent when HUVECs were incubated in the presence of conditioned medium form nuclear decorin silenced dysplastic and malignant cell lines as compared to respective controls.
Conclusions:
Together these results indicate that aberrantly expressed nuclear localized decorin strongly influences angiogenic potential of dysplastic and malignant oral epithelial cells.</description>
        <link>http://www.headandneckoncology.org/content/4/1/11</link>
                <dc:creator>Nyla Dil</dc:creator>
                <dc:creator>Abhijit Banerjee</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2012, null:11</dc:source>
        <dc:date>2012-04-16T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-4-11</dc:identifier>
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        <item rdf:about="http://www.headandneckoncology.org/content/4/1/19">
        <title>Systemic therapy in the management of metastatic or advanced salivary gland cancers</title>
        <description>Salivary gland cancers are very rare tumors. They are characterized by a histologic heterogeneity and a poor outcome. According to this rarity, few prospective data are available to date. No standard recommendations could be held for the use of systemic therapy in these tumors. Several case reports and small studies have investigated the contribution of different agents of chemotherapy. With the extension of molecular biology approach in oncology several signaling pathways have been discovered in different cancers including salivary gland cancers; thus a number of targeted therapies have been investigated. This paper reviewed exhaustively the studies investigating the role of systemic therapies (chemotherapy, targeted therapy, hormone therapy) in salivary gland cancers.</description>
        <link>http://www.headandneckoncology.org/content/4/1/19</link>
                <dc:creator>Aymen Lagha</dc:creator>
                <dc:creator>Nesrine Chraiet</dc:creator>
                <dc:creator>Mouna Ayadi</dc:creator>
                <dc:creator>Sarra Krimi</dc:creator>
                <dc:creator>Bassem Allani</dc:creator>
                <dc:creator>Hela Rifi</dc:creator>
                <dc:creator>Henda Raies</dc:creator>
                <dc:creator>Amel Mezlini</dc:creator>
                <dc:source>Head &amp; Neck Oncology 2012, null:19</dc:source>
        <dc:date>2012-05-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1758-3284-4-19</dc:identifier>
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