<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JCT</journal-id><journal-title-group><journal-title>Journal of Cancer Therapy</journal-title></journal-title-group><issn pub-type="epub">2151-1934</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jct.2013.43091</article-id><article-id pub-id-type="publisher-id">JCT-31610</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Multimodality Treatment for Thymic Carcinoma: Review of 11 Cases at a Single Institute
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>isao</surname><given-names>Higo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Keiichi</surname><given-names>Fujiwara</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Go</surname><given-names>Makimoto</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yuhei</surname><given-names>Tokimasa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nobuhisa</surname><given-names>Kameyama</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mizuho</surname><given-names>Matsushita</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kammei</surname><given-names>Rai</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ken</surname><given-names>Sato</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Takuo</surname><given-names>Shibayama</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Toshiro</surname><given-names>Yonei</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Akio</surname><given-names>Andou</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Toshio</surname><given-names>Sato</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Respiratory Medicine, National Hospital Organization Okayama Medical Center, Okayama, Japan</addr-line></aff><aff id="aff2"><addr-line>Department of Respiratory Surgery, National Hospital Organization Okayama Medical Center, Okayama, Japan</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>h_hisao_430@yahoo.co.jp(KF)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>22</day><month>05</month><year>2013</year></pub-date><volume>04</volume><issue>03</issue><fpage>742</fpage><lpage>746</lpage><history><date date-type="received"><day>March</day>	<month>20th,</month>	<year>2013</year></date><date date-type="rev-recd"><day>April</day>	<month>22nd,</month>	<year>2013</year>	</date><date date-type="accepted"><day>April</day>	<month>30th,</month>	<year>2013</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   <b>Background:</b> We reported our experience with thymic carcinomas and review their clinical features, treatment strategies, and prognoses. <b>Methods:</b> From April 1998 to November 2012, 11 patients pathologically diagnosed with thymic carcinoma and treated in our hospital were investigated. <b>Results:</b> There were 7 men and 4 women, with a median age of 62 years (range, 35 - 72). According to the Masaoka staging system, 3 patients had stage II, 1 stage III disease, 3 stage IVa disease and 4 stage IVb disease. Ten patients had squamous cell carcinoma, whereas 1 had large cell neuroendocrine carcinoma (LCNEC). We performed surgery or multimodality therapy including surgery as the initial therapy for 8 patients. Of the non-surgical cases, 1 patient received chemoradiotherapy and survived for over 6 years without recurrence, whereas 2 received palliative care. Three of 4 patients who underwent complete resection survived without disease recurrence, whereas only 1 patient with LCNEC survived in the incomplete resection group. Multimodality therapy with cisplatin and docetaxel was provided to 3 patients, and recurrence has not been observed in any of the cases. <b>Conclusions:</b> Favorable outcomes could be achieved in patients with thymic carcinoma who underwent intensive treatment. In particular, surgery combined with cisplatin and docetaxel plus thoracic irradiation may be an attractive approach for thymic carcinoma. 
 
</p></abstract><kwd-group><kwd>Thymic Carcinoma; Multimodality Treatment; Cisplatin; Docetaxel</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Thymic carcinoma is a rare tumor arising from the thymic epithelium that accounts for approximately 14.1% of thymic epithelial neoplasms and differs from thymoma with respect to morphological and biological features. The most common histologic type in Japan is squamous cell carcinoma [<xref ref-type="bibr" rid="scirp.31610-ref1">1</xref>]. The prognosis of thymic carcinoma is worse than that of thymoma, with a 5-year survival rate of 33.3% to 50.5%, which correlates with the Masaoka staging system [1,2]. Unfortunately, 80% to 90% of cases are diagnosed at an advanced stage (stage III or IV) [1,3]. Treatment with surgery, radiotherapy, and chemotherapy has been described in some reports, but there is no consensus as to which modality or combined modality is the gold standard. We report our experience with 11 cases of thymic carcinoma and review their clinical features, treatment, and prognoses.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>From April 1998 to November 2012, 11 patients were pathologically diagnosed with thymic carcinoma and treated in our hospital. We retrospectively reviewed their clinical features, treatment, and prognoses. The clinical or pathological stage of the disease was determined according to the staging system described by Masaoka et al. [<xref ref-type="bibr" rid="scirp.31610-ref4">4</xref>]. The pathological diagnosis of thymic carcinoma was established according to the histopathological criteria proposed by the World Health Organization (WHO) [<xref ref-type="bibr" rid="scirp.31610-ref5">5</xref>].</p><p>Overall survival time was calculated from the date of diagnosis until death or the last follow-up visit using the Kaplan-Meier method. Statistical analyses were performed using SPSS version 20 for Windows (IBM).</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Patient Characteristics</title><p>The study included 7 men and 4 women, with a median age of 62 years (range, 35 - 72). According to the Masaoka staging system, 3 patients had stage II disease, 1 stage III disease, 3 stage IVa disease and 4 stage IVb disease. Pathologically, 10 patients had squamous cell carcinoma, whereas 1 had large cell neuroendocrine carcinoma (LCNEC). We performed surgery or multimodality therapy including surgery as the initial therapy for 8 patients. Of the non-surgical cases, 1 patient received chemoradiotherapy, whereas 2 received palliative care.</p></sec><sec id="s3_2"><title>3.2. Treatment Strategies and Clinical Outcomes</title><p><xref ref-type="table" rid="table1">Table 1</xref> summarizes all cases with respect to their initial treatment and respective outcomes. One patient (case 7) from the non-surgery group received pericardial drainage and died 21 months after the diagnosis. A second patient (case 8) was treated with radiotherapy to the site of bone metastasis followed by chemotherapy and eventually died 23 months later. Another patient (case 9) received chemotherapy consisting of cisplatin and docetaxel with concurrent thoracic irradiation in accordance with the OLCSG 0007 protocol [<xref ref-type="bibr" rid="scirp.31610-ref6">6</xref>]; this patient is still alive 6 years later without disease progression (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>In the surgical intervention group, 1 patient received surgery alone, 2 patients received surgery and adjuvant radiotherapy, 3 patients received surgery with adjuvant chemotherapy and subsequent radiotherapy, and 2 patients received preoperative chemoradiotherapy, surgery, and adjuvant chemotherapy. Complete resection was performed in 4 of the 8 cases (<xref ref-type="table" rid="table2">Table 2</xref>). In the complete resection group, 3 of 4 patients were alive and disease free at the time of reporting, whereas the other patient (case 2) had recurrence of pleural dissemination. In the incomplete resection group, 1 patient with LCNEC was alive with no evidence of disease following postoperative radiotherapy and chemotherapy consisting of carboplatin and etoposide at the time of reporting.</p><p>However, the other 3 patients experienced disease recurrence. As shown in <xref ref-type="table" rid="table2">Table 2</xref>, better outcomes were achieved in patients at an early Masaoka stage and in those who underwent complete resection together with radiotherapy and chemotherapy.</p><p><xref ref-type="table" rid="table3">Table 3</xref> shows the site of disease recurrence in each patient who received surgery. Manifestations of disease recurrence were dissemination to the pleura, supraclavicular lymph nodes, and lungs. Seven of the 11 patients are still alive. The median survival time and 5-year survival rate were 63.7 months and 58.3%, respectively.</p></sec></sec></body><back><ref-list><title>References</title><ref id="scirp.31610-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">K. Kondo and T. Monden, “Therapy for Thymic Epithelial Tumors: A Clinical Study of 1320 Patients from Japan,” The Annals of Thoracic Surgery, Vol.76, No. 3, 2003, pp. 878-884. doi:10.1016/S0003-4975(03)00555-1</mixed-citation></ref><ref id="scirp.31610-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">S. Suster and J. Rosai, “Thymic Carcinoma. A Clinicopathologic Study of 60 Patients,” Cancer, Vol. 67, No. 4, 1991, pp. 1025-1032.  
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