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    <title>AMA Publishing Group: Oncology Topic Collection</title>
    <link>http://pubs.jamanetwork.com/</link>
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    <pubDate>Thu, 16 May 2013 00:00:00 GMT</pubDate>
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      <title>An Oral Cavity Carcinoma Nomogram to Predict Benefit of Adjuvant Radiotherapy Oral Cavity Adjuvant Radiotherapy Prediction Model </title>
      <link>http://pubs.jamanetwork.com/article.aspx?articleID=1686141</link>
      <pubDate>Thu, 16 May 2013 00:00:00 GMT</pubDate>
      <author>Wang SJ, Patel SG, Shah JP, et al. </author>
      <description>&lt;span class="paragraphSection"&gt;&lt;div class="boxTitle"&gt;Importance&lt;/div&gt;After surgical resection for oral cavity squamous cell carcinoma, adjuvant radiotherapy may be recommended for patients at higher risk for locoregional recurrence, but it can be difficult to predict whether a particular patient will benefit.&lt;div class="boxTitle"&gt;Objective&lt;/div&gt;To construct a model to predict which patients with oral cavity squamous cell carcinoma would benefit from adjuvant radiotherapy.&lt;div class="boxTitle"&gt;Design and Setting&lt;/div&gt;We constructed several types of survival models using a set of 979 patients with oral cavity squamous cell carcinoma. Covariates were age, sex, tobacco use, stage, grade, margins, and subsite. The best performing model was externally validated on a set of 431 patients.&lt;div class="boxTitle"&gt;Participants&lt;/div&gt;The model was based on a set of 979 patients with oral cavity squamous cell carcinoma, including 563 from Memorial Sloan Kettering Cancer Center, New York, New York, and 416 from the Hospital AC Camargo, São Paulo, Brazil. The validation set consisted of 431 patients from Princess Margaret Hospital, Toronto, Ontario, Canada.&lt;div class="boxTitle"&gt;Main Outcome and Measure&lt;/div&gt;The primary outcome measure of interest was locoregional recurrence-free survival.&lt;div class="boxTitle"&gt;Results&lt;/div&gt;The lognormal model showed the best performance per the Akaike information criterion. An online nomogram was built from this model that estimates locoregional failure-free survival with and without postoperative radiotherapy.&lt;div class="boxTitle"&gt;Conclusions and Relevance&lt;/div&gt;A web-based nomogram can be used as a decision aid for adjuvant treatment decisions for patients with oral cavity squamous cell carcinoma.&lt;/span&gt;</description>
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      <prism:doi xmlns:prism="prism">10.1001/jamaoto.2013.3001</prism:doi>
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      <title>Association of Ocular and Oculodermal Melanocytosis With the Rate of Uveal Melanoma Metastasis Analysis of 7872 Consecutive Eyes  Oculo(dermal) Melanocytosis and Uveal Melanoma </title>
      <link>http://pubs.jamanetwork.com/article.aspx?articleID=1687776</link>
      <pubDate>Thu, 16 May 2013 00:00:00 GMT</pubDate>
      <author>Shields CL, Kaliki S, Livesey M, et al. </author>
      <description>&lt;span class="paragraphSection"&gt;&lt;div class="boxTitle"&gt;Importance&lt;/div&gt;Ocular/oculodermal (oculo[dermal]) melanocytosis is a congenital periocular pigmentary condition that can lead to the development of uveal melanoma, estimated at 1 in 400 affected patients. In this study, patients with melanocytosis who developed uveal melanoma were found to have double the risk for metastasis compared with those without melanocytosis.&lt;div class="boxTitle"&gt;Objective&lt;/div&gt;To determine the relationship of oculo(dermal) melanocytosis to the prognosis of patients with uveal melanoma.&lt;div class="boxTitle"&gt;Design, Setting, and Patients&lt;/div&gt;Retrospective chart review of 7872 patients with uveal melanoma treated at the Ocular Oncology Service, Wills Eye Institute, from August 25, 1970, through August 27, 2008.&lt;div class="boxTitle"&gt;Exposures&lt;/div&gt;Enucleation, plaque radiotherapy, local resection, or thermotherapy.&lt;div class="boxTitle"&gt;Main Outcomes and Measures&lt;/div&gt;Metastasis and death.&lt;div class="boxTitle"&gt;Results&lt;/div&gt;Of 7872 patients with uveal melanoma, oculo(dermal) melanocytosis was present in 230 (3%). The melanocytosis involved the sclera (92%), iris (17%), choroid (12%), eyelid (8%), and temporal fossa (1%). Eyes with melanoma and oculo(dermal) melanocytosis had a relative risk for metastasis 1.6 times greater compared with those with no melanocytosis (P &lt; .001). Metastasis of uveal melanoma was 2.8 times higher in patients with iris melanocytosis (P &lt; .001), 2.6 times higher with choroidal melanocytosis (P = .02), and 1.9 times higher with scleral melanocytosis (P &lt; .001). By Kaplan-Meier estimates, metastasis in patients with oculo(dermal) melanocytosis vs no melanocytosis was 2% vs 1.8% at 1 year, 27% vs 15% at 5 years, and 48% vs 24% at 10 years (P &lt; .001). By multivariable analysis, the factors predictive of metastasis in patients harboring uveal melanoma associated with oculo(dermal) melanocytosis were increased tumor thickness (P = .001) and the presence of subretinal fluid (P = .05), and the only factor predictive of death was increased tumor thickness (P = .009).&lt;div class="boxTitle"&gt;Conclusions and Relevance&lt;/div&gt;Patients with uveal melanoma associated with oculo(dermal) melanocytosis have double the risk for metastasis compared with those with no melanocytosis. All patients with oculo(dermal) melanocytosis should undergo ophthalmic examination and imaging on a twice-yearly basis because this could help with the early detection of melanoma.&lt;/span&gt;</description>
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      <prism:doi xmlns:prism="prism">10.1001/jamaophthalmol.2013.129</prism:doi>
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