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	<title>Mesothelioma Journal Articles &#187; Surgery</title>
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	<description>Journal Articles on Mesothelioma: Cancer Information for Patients and Families</description>
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		<title>Accuracy of diagnostic biopsy for the histological subtype of malignant pleural mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2011/01/26/accuracy-of-diagnostic-biopsy-for-the-histological-subtype-of-malignant-pleural-mesothelioma/</link>
		<comments>http://www.mesothelioma-line.com/articles/2011/01/26/accuracy-of-diagnostic-biopsy-for-the-histological-subtype-of-malignant-pleural-mesothelioma/#comments</comments>
		<pubDate>Wed, 26 Jan 2011 19:53:00 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Biphasic or Mixed]]></category>
		<category><![CDATA[CT or CAT scan]]></category>
		<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Epithelioid]]></category>
		<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[thoracoscopy]]></category>
		<category><![CDATA[thoracotomy]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1705</guid>
		<description><![CDATA[Journal of Thoracic Oncology. 2011 Mar;6(3):602-5. [Link] Kao SC, Yan TD, Lee K, Burn J, Henderson DW, Klebe S, Kennedy C, Vardy J, Clarke S, van Zandwijk N, McCaughan BC. Asbestos Diseases Research Institute, Bernie Banton Centre, Sydney, Australia. Abstract Introduction: Histological subtype is an established prognostic factor in malignant pleural mesothelioma (MPM). We retrospectively [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal of Thoracic Oncology</em>. 2011 Mar;6(3):602-5. [<a href="http://journals.lww.com/jto/pages/articleviewer.aspx?year=2011&amp;issue=03000&amp;article=00028&amp;type=abstract">Link</a>]</p>
<p><strong>Kao SC, Yan TD, Lee K, Burn J, Henderson DW, Klebe S, Kennedy C, Vardy J, Clarke S, van Zandwijk N, McCaughan BC.</strong></p>
<p>Asbestos Diseases Research Institute, Bernie Banton Centre, Sydney, Australia.</p>
<h3>Abstract</h3>
<p><strong>Introduction: </strong> Histological  subtype is an established prognostic factor in malignant pleural  mesothelioma (MPM). We retrospectively investigated the accuracy of  classifying histological subtype on diagnostic biopsies and examined the  impact of different diagnostic procedures on the outcome.</p>
<p><strong>Methods: </strong> Consecutive  patients with histologically confirmed MPM who underwent extrapleural  pneumonectomy (EPP) from 1994 to 2009 were included. Patient records  were reviewed, and the initial diagnoses of histological subtype were  obtained. The archival EPP specimens were reviewed by a panel of  pathologists. The histological subtype obtained at review was compared  with the initial diagnosis.</p>
<p><strong>Results: </strong> Eighty-five patients  underwent EPP. Two patients achieved a pathological complete response  after neoadjuvant chemotherapy, leaving 83 patients to be included in  this review. Different diagnostic methods were used before EPP: 81%  thoracoscopy; 7% thoracotomy; 11% computed tomography-guided procedure;  and 1% other. Patients determined to have an epithelial subtype (n = 64)  at EPP were diagnosed correctly at initial diagnostic biopsy in 84% of  cases, whereas patients considered to have a biphasic subtype (n = 19)  at EPP were diagnosed correctly at diagnostic biopsy in 26% of cases.  The sensitivity and specificity of diagnostic biopsy for epithelial MPM  was 93% and 31%, respectively. The overall subtype misclassification  rate was 20%. Biopsy by thoracotomy was most accurate in subtype  classification (83%) compared with thoracoscopy (74%) and computed  tomography-guided procedure (44%).</p>
<p><strong>Conclusions: </strong> The  determination of histological subtype from a diagnostic biopsy is  difficult due to sampling error, but an adequate specimen obtained from  surgical biopsy increases the accuracy of subtype classification  compared with radiological-guided biopsies.</p>
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		<item>
		<title>Thoracoscopic extrapleural pneumonectomy for mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2011/01/25/thoracoscopic-extrapleural-pneumonectomy-for-mesothelioma/</link>
		<comments>http://www.mesothelioma-line.com/articles/2011/01/25/thoracoscopic-extrapleural-pneumonectomy-for-mesothelioma/#comments</comments>
		<pubDate>Tue, 25 Jan 2011 18:14:51 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1698</guid>
		<description><![CDATA[The Annals of thoracic surgery. 2011 Feb;91(2):616-8. [Link] Demmy TL, Platis IE, Nwogu C, Yendamuri S. Department of Thoracic Surgery, Roswell Park Cancer Institute, Buffalo, New York. Abstract Mesothelioma is the most common primary pleural malignancy. Surgical therapy offers limited cure benefits at the cost of high morbidity. Although technically challenging and performed rarely, a [...]]]></description>
			<content:encoded><![CDATA[<p>The Annals of thoracic surgery. 2011 Feb;91(2):616-8. [<a href="http://www.sciencedirect.com/science?_ob=ArticleURL&amp;_udi=B6T11-520CR5P-2Y&amp;_user=10&amp;_coverDate=02/28/2011&amp;_rdoc=1&amp;_fmt=high&amp;_orig=search&amp;_origin=search&amp;_sort=d&amp;_docanchor=&amp;view=c&amp;_acct=C000050221&amp;_version=1&amp;_urlVersion=0&amp;_userid=10&amp;md5=c5746e593f99f152b076501919cbdbe7&amp;searchtype=a">Link</a>]</p>
<p><strong>Demmy TL, Platis IE, Nwogu C, Yendamuri S.</strong></p>
<p>Department of Thoracic Surgery, Roswell Park Cancer Institute, Buffalo, New York.</p>
<h3>Abstract</h3>
<p>Mesothelioma  is the most common primary pleural malignancy. Surgical therapy offers  limited cure benefits at the cost of high morbidity. Although  technically challenging and performed rarely, a less invasive approach  to extrapleural pneumonectomy was developed with the intent to speed  convalescence, hasten adjuvant therapies, improve quality of life, and  reduce wound surface area for possible tumor contamination.</p>
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		<title>Biological Materials for Diaphragmatic Repair: Initial Experiences with the PeriGuard Repair Patch&#174;</title>
		<link>http://www.mesothelioma-line.com/articles/2011/01/19/biological-materials-for-diaphragmatic-repair-initial-experiences-with-the-periguard-repair-patch/</link>
		<comments>http://www.mesothelioma-line.com/articles/2011/01/19/biological-materials-for-diaphragmatic-repair-initial-experiences-with-the-periguard-repair-patch/#comments</comments>
		<pubDate>Wed, 19 Jan 2011 19:45:06 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Determining Efficacy]]></category>
		<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1681</guid>
		<description><![CDATA[The Thoracic and Cardiovascular Surgeon. 2011 Feb;59(1):40-4. Epub 2011 Jan 17. [Link] Zardo P, Zhang R, Wiegmann B, Haverich A, Fischer S. Department of Thoracic Surgery and Lung Assist, Klinikum Ibbenbüren, Ibbenbüren, Germany. Abstract Background: We sought to analyze the efficacy of a bovine pericardial patch (PeriGuard®) for diaphragmatic repair. Methods: Seven consecutive patients (6 [...]]]></description>
			<content:encoded><![CDATA[<p><em>The Thoracic and Cardiovascular Surgeon</em>. 2011 Feb;59(1):40-4. Epub 2011 Jan 17. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/21243571">Link</a>]</p>
<p><strong>Zardo P, Zhang R, Wiegmann B, Haverich A, Fischer S.</strong></p>
<p>Department of Thoracic Surgery and Lung Assist, Klinikum Ibbenbüren, Ibbenbüren, Germany.</p>
<h3>Abstract</h3>
<p><strong>Background</strong>: We sought to analyze the efficacy of a bovine pericardial patch (PeriGuard®) for diaphragmatic repair.</p>
<p><strong>Methods</strong>: Seven consecutive patients (6 males, median age 56 years) scheduled for diaphragmatic resection and/or repair were enrolled in this study. In all cases diaphragmatic repair was performed with a PeriGuard Repair Patch® (Synovis, St. Paul, MN, USA). At follow-up (median: 12 months; range: 6-18 months), quality of life, signs of reherniation and incorporation of mesh were assessed through clinical examination, blood samples and CT or MRT scan.</p>
<p><strong>Results</strong>: Diagnosis on admission included sarcoma (n = 2), mesothelioma (n = 1), squamous cell carcinoma (n = 1), parachordoma (n = 1) and large congenital or posttraumatic herniation (n = 2). At follow-up successful diaphragmatic repair with no signs of reherniation, graft dehiscence or seroma formation was confirmed for all patients. Recorded inflammatory markers [C-reactive protein (CRP), white blood cell count (WBC) and procalcitonin (PCT)] reached their peak values between postoperative day (POD) 4 and POD 7. Values ranged from 122-282 mg/L for CRP, 0.4-4.6 µg/L for PCT and 6.2-15.6 Tsd/µL for WBC. Overall oncological results were good and 5 out of 6 survivors reported a fully reestablished quality of life.</p>
<p><strong>Conclusion</strong>: We consider the PeriGuard Repair Patch&reg; a viable alternative to synthetic materials for diaphragm replacement. Moreover, we advise carrying out cautious follow-up in patients undergoing extensive oncological resection to learn more about the biological behavior of the bovine PeriGuard Repair Patch® after diaphragmatic repair.</p>
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		<item>
		<title>Indication of Peritonectomy for Peritoneal Dissemination</title>
		<link>http://www.mesothelioma-line.com/articles/2011/01/13/indication-of-peritonectomy-for-peritoneal-dissemination/</link>
		<comments>http://www.mesothelioma-line.com/articles/2011/01/13/indication-of-peritonectomy-for-peritoneal-dissemination/#comments</comments>
		<pubDate>Thu, 13 Jan 2011 18:35:55 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Chemotherapy]]></category>
		<category><![CDATA[Determining Efficacy]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Intraperitoneal Chemotherapy]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
		<category><![CDATA[Peritonectomy]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Survival]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1648</guid>
		<description><![CDATA[Gan To Kagaku Ryoho. 2010 Nov;37(12):2306-2311. [Link] Yonemura Y, Tsukiyama G, Miyata R, Sako S, Endou Y, Hirano M, Mizumoto A, Matsuda T, Takao N, Ichinose M, Miura M, Hagiwara A, Li Y. NPO Organization to Support Peritoneal Dissemination Treatment. Abstract A total of 521 patients with peritoneal carcinomatosis (PC) were treated by peritonectomy and [...]]]></description>
			<content:encoded><![CDATA[<p><em>Gan To Kagaku Ryoho</em>. 2010 Nov;37(12):2306-2311. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/21224556">Link</a>]</p>
<p><strong>Yonemura Y, Tsukiyama G, Miyata R, Sako S, Endou Y, Hirano M, Mizumoto A, Matsuda T, Takao N, Ichinose M, Miura M, Hagiwara A, Li Y.</strong></p>
<p>NPO Organization to Support Peritoneal Dissemination Treatment.</p>
<h3>Abstract</h3>
<p>A total of 521 patients with peritoneal carcinomatosis (PC) were treated  by peritonectomy and perioperative chemotherapy. Each of the 95, 58,  316, 31, 10 and 11 patients were from gastric, colorectal, appendiceal,  ovarian, small bowel cancer and mesothelioma, respectively. The  distribution and volume of PC are recorded by the Sugarbaker peritoneal  carcinomatosis index( PCI). Peritonectomy was performed with a radical  resection of the primary tumor and all gross PC with involved organs,  peritoneum, or tissue that was deemed technically feasible and safe for  the patient. The postoperative major complication of grade 3 was found  in 14%, and total 30 &#8211; day mortality was 2.7%. The survival of gastric  cancer patients with a PCI score &le; 6 was significantly better than those  with a PCI score &ge; 7. In appendiceal neoplasm, patients with PCI score  less than 28 showed significantly better survival than those with PCI  score greater than 29. The survival of colorectal cancer patients with a  PCI score &ge; 11 was significantly poorer than those with a PCI score &le;  10. Among the various prognostic factors in appendiceal neoplasm and  gastric cancer patients, CC &#8211; 0 complete cytoreduction was the most  important independent prognostic factor. Peritonectomy is done to remove  macroscopic disease and perioperative intraperitoneal chemotherapy to  eradicate microscopic residual disease aiming to remove disease  completely with a single procedure. Peritonectomy combined with  perioperative chemotherapy may achieve long &#8211; term survival in a  selected group of patients with PC. The higher mortality rate underlines  this necessarily strict selection that should be reserved to  experienced institutions.</p>
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		<title>Peritoneal mesothelioma: treatment with cytoreductive surgery combined with hyperthermic intraperitoneal chemotherapy</title>
		<link>http://www.mesothelioma-line.com/articles/2008/12/25/peritoneal-mesothelioma-treatment-with-cytoreductive-surgery-combined-with-hyperthermic-intraperitoneal-chemotherapy/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/12/25/peritoneal-mesothelioma-treatment-with-cytoreductive-surgery-combined-with-hyperthermic-intraperitoneal-chemotherapy/#comments</comments>
		<pubDate>Thu, 25 Dec 2008 15:01:42 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Chemotherapy]]></category>
		<category><![CDATA[Determining Efficacy]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Intraperitoneal Chemotherapy]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Survival]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Tumor Debulking]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1620</guid>
		<description><![CDATA[Journal de Chirurgie Viscérale. 2008 Sep-Oct;145(5):447-53.[Article in French] [Link] Passot G, Cotte E, Brigand C, Beaujard AC, Isaac S, Gilly FN, Glehen O. Service de chirurgie générale digestive et endocrinienne, centre hospitalier Lyon Sud (CHLS) &#8211; Lyon. Abstract Diffuse malignant peritoneal mesothelioma is a rare and lethal disease. Locoregional treatments combining cytoreductive surgery with hyperthermic [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal de Chirurgie Viscérale</em>. 2008 Sep-Oct;145(5):447-53.[Article in French] [<a href="http://www.em-consulte.com/article/194833">Link</a>]</p>
<p><strong>Passot G, Cotte E, Brigand C, Beaujard AC, Isaac S, Gilly FN, Glehen O.</strong></p>
<p>Service de chirurgie générale digestive et endocrinienne, centre hospitalier Lyon Sud (CHLS) &#8211; Lyon.</p>
<h3>Abstract</h3>
<p>Diffuse malignant peritoneal mesothelioma is a rare and lethal disease. Locoregional treatments combining cytoreductive surgery with hyperthermic intraperitoneal chemotherapy (HIPEC) seem to improve prognosis.</p>
<p><strong>Methods</strong>: Cytoreductive surgery and HIPEC was performed in 22 patients at the Centre Hospitalier-Lyon Sud between 1989 and 2006. A retrospective analysis of survival was carried out to assess clinical and histological prognostic factors.</p>
<p><strong>Results</strong>: Nineteen patients with diffuse malignant peritoneal mesothelioma were included (16 epithelial, 3 biphasic and 3 multicystic forms). Sixteen patients presented stage 3 or 4 peritoneal carcinomatosis according to the Gilly classification. Optimal cytoreductive surgery was performed for 11 patients (complete macroscopic resection or residual tumor nodules less than 2.5mm). No post-operative deaths occurred but 9 patients (47%) presented grade III or IV post-operative complications. The overall median survival was 36.9 months; completeness of cytoreduction was the only significant prognostic factor.</p>
<p><strong>Conclusion</strong>: Cytoreductive surgery combined with HIPEC may improve the length of survival for patients with diffuse malignant peritoneal mesothelioma; such patients should be treated in specialized centers.</p>
<p><strong>Keywords</strong>: Peritoneal Mesothelioma , Treatment , Cytoreductive surgery , Hyperthermic intraperitoneal chemotherapy</p>
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		<title>Vitamin D-mediated hypercalcemia and Cushing syndrome as manifestations of malignant pleural mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/12/20/vitamin-d-mediated-hypercalcemia-and-cushing-syndrome-as-manifestations-of-malignant-pleural-mesothelioma/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/12/20/vitamin-d-mediated-hypercalcemia-and-cushing-syndrome-as-manifestations-of-malignant-pleural-mesothelioma/#comments</comments>
		<pubDate>Sat, 20 Dec 2008 14:37:49 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Case Study]]></category>
		<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Immunohistochemistry or IHC]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1610</guid>
		<description><![CDATA[Endocrine Practice. 2008 Nov;14(8):1011-6. [Link] Lee JM, Pou K, Sadow PM, Chen H, Hu B, Hewison M, Adams JS, Sugarbaker DJ, Fisher ND. Division of Thoracic Surgery, Brigham and Women&#8217;s Hospital, Harvard Medical School, Boston, MA, USA. jaymoonlee@mednet.ucla.edu Abstract Objective: To report a case of coincident hypercalcemia and Cushing syndrome arising from mesothelioma. Methods: We [...]]]></description>
			<content:encoded><![CDATA[<p><em>Endocrine Practice</em>. 2008 Nov;14(8):1011-6. [<a href="http://aace.metapress.com/app/home/contribution.asp?referrer=parent&#038;backto=issue,9,19;journal,14,110;linkingpublicationresults,1:300404,1">Link</a>]</p>
<p><strong>Lee JM, Pou K, Sadow PM, Chen H, Hu B, Hewison M, Adams JS, Sugarbaker DJ, Fisher ND.</strong></p>
<p>Division of Thoracic Surgery, Brigham and Women&#8217;s Hospital, Harvard Medical School, Boston, MA, USA. jaymoonlee@mednet.ucla.edu</p>
<h3>Abstract</h3>
<p><strong>Objective</strong>: To report a case of coincident hypercalcemia and Cushing syndrome arising from mesothelioma.</p>
<p><strong>Methods</strong>: We describe the clinical, laboratory, imaging, and pathologic findings of a patient with malignant pleural mesothelioma and elucidate the underlying biologic mechanisms resulting in concurrent overexpression of steroid and polypeptide hormones.</p>
<p><strong>Results</strong>: A 62-year-old woman presented with chest discomfort and cough. Radiologic imaging revealed a diffuse pleural-based mass encasing the right lung. There was no invasion into the chest wall, diaphragm, or mediastinum, and there was no distant disease. Laboratory analyses documented hypercalcemia and Cushing syndrome, which were due to ectopic overproduction of 1,25-dihydroxyvitamin D (1,25[OH]<sub>2</sub>D) and corticotropin. Surgical resection resulted in normocalcemia with normalization of serum 1,25(OH)<sub>2</sub>D and reduction in hypercortisolemia. The extrapleural pneumonectomy specimen revealed overexpression of the 1,25(OH)<sub>2</sub>D synthetic enzyme 25-hydroxyvitamin-D-1alpha-hydroxylase (1alpha-hydroxylase) and underexpression of the 1,25(OH)<sub>2</sub>D catabolic enzyme 24-hydroxylase. Immunohistochemistry and electron microscopy demonstrated corticotropin and secretory granules in the tumor tissue.</p>
<p><strong>Conclusion</strong>: These findings support the evidence for a paracrine role of vitamin D in the resistance of the human host to antigen.</p>
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		<title>Diffuse Malignant Peritoneal Mesothelioma: Failure Analysis Following Cytoreduction and Hyperthermic Intraperitoneal Chemotherapy (HIPEC)</title>
		<link>http://www.mesothelioma-line.com/articles/2008/12/17/diffuse-malignant-peritoneal-mesothelioma-failure-analysis-following-cytoreduction-and-hyperthermic-intraperitoneal-chemotherapy-hipec/</link>
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		<pubDate>Wed, 17 Dec 2008 17:26:29 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Chemotherapy]]></category>
		<category><![CDATA[Determining Efficacy]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Intraperitoneal Chemotherapy]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Survival]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Tumor Debulking]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1577</guid>
		<description><![CDATA[Annals of Surgical Oncology. 2009 Feb;16(2):463-72. Epub 2008 Dec 12. [Link] Baratti D, Kusamura S, Cabras AD, Dileo P, Laterza B, Deraco M. Department of Surgery, National Cancer Institute, Milan, Italy. Abstract Improved survival has been reported for diffuse malignant peritoneal mesothelioma (DMPM) treated by cytoreduction and hyperthermic intraperitoneal chemotherapy (HIPEC). The issue of treatment [...]]]></description>
			<content:encoded><![CDATA[<p><em>Annals of Surgical Oncology</em>. 2009 Feb;16(2):463-72. Epub 2008 Dec 12. [<a href="http://www.springerlink.com/content/e49947h742th5071/">Link</a>]</p>
<p><strong>Baratti D, Kusamura S, Cabras AD, Dileo P, Laterza B, Deraco M.</strong></p>
<p>Department of Surgery, National Cancer Institute, Milan, Italy.</p>
<h3>Abstract</h3>
<p>Improved survival has been reported for diffuse malignant peritoneal mesothelioma (DMPM) treated by cytoreduction and hyperthermic intraperitoneal chemotherapy (HIPEC). The issue of treatment failure has never been extensively addressed. The present study assessed the failure pattern, management, and outcome of progressive DMPM following comprehensive treatment. Clinical data on 70 patients with DMPM undergoing cytoreduction and HIPEC were prospectively collected; after a median follow-up of 43 months, disease progression occurred in 38 patients. Progressive disease distribution in 13 abdominopelvic regions was analyzed. In 28 patients undergoing adequate cytoreduction (residual tumor &lt; or =2.5 mm), clinicopathological factors correlating to disease progression in each region were investigated. Median time to progression was 9 months [95% confidence interval (CI) 1.6-35.9]. Median survival from progression was 8 months (95% CI 4-16.2). The failure pattern was categorized as peritoneal progression (n = 31), liver metastases (n = 1), abdominal lymph-node involvement (n = 2), pleural seeding (n = 4). Small bowel was the single site most commonly involved (n = 27). Residual tumor &lt; or =2.5 mm (versus no visible) was the only independent risk factor for disease progression in epigastric region (P = 0.047), upper ileum (P = 0.029), upper jejunum (P = 0.034), and lower jejunum (P = 0.002). Progressive disease was treated with second HIPEC in 3 patients, debulking in 4, systemic chemotherapy in 16, and supportive care in 15. At multivariate analysis, time to progression &lt;9 months (P = 0.009), poor performance status (P = 0.005), and supportive care (P = 0.003) correlated to reduced survival from progression. We conclude that minimal residual disease, compared with macroscopically complete cytoreduction, correlated to failure in critical anatomical areas, suggesting the need for maximal cytoreductive surgical efforts. In selected patients, aggressive management of progressive disease seems worthwhile.</p>
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		<title>Cytoreductive surgery and continuous hyperthermic peritoneal perfusion in patients with mesothelioma and peritoneal carcinomatosis: hemodynamic, metabolic, and anesthetic considerations</title>
		<link>http://www.mesothelioma-line.com/articles/2008/12/04/cytoreductive-surgery-and-continuous-hyperthermic-peritoneal-perfusion-in-patients-with-mesothelioma-and-peritoneal-carcinomatosis-hemodynamic-metabolic-and-anesthetic-considerations/</link>
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		<pubDate>Thu, 04 Dec 2008 16:29:45 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Chemotherapy]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Intraperitoneal Chemotherapy]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Tumor Debulking]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1566</guid>
		<description><![CDATA[Annals of Surgical Oncology. 2009 Feb;16(2):334-44. Epub 2008 Dec 3. [Link] Miao N, Pingpank JF, Alexander HR, Royal R, Steinberg SM, Quezado MM, Beresnev T, Quezado ZM. Department of Anesthesia and Surgical Services, National Institutes of Health Clinical Center, National Institutes of Health, 10 Center Drive, MSC-1512, Building 10, Room 2C624, Bethesda, MD 20892-1512, USA. [...]]]></description>
			<content:encoded><![CDATA[<p><em>Annals of Surgical Oncology</em>. 2009 Feb;16(2):334-44. Epub 2008 Dec 3. [<a href="http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&amp;pubmedid=19050961" target="_blank">Link</a>]</p>
<p><strong>Miao N, Pingpank JF, Alexander HR, Royal R, Steinberg SM, Quezado MM, Beresnev T, Quezado ZM.</strong></p>
<p>Department of Anesthesia and Surgical Services, National Institutes of Health Clinical Center, National Institutes of Health, 10 Center Drive, MSC-1512, Building 10, Room 2C624, Bethesda, MD 20892-1512, USA.</p>
<h3 class="abstract">Abstract</h3>
<p>Cytoreductive surgery and continuous hyperthermic peritoneal perfusion (CHPP) involve the conduct of a complex surgical procedure and delivery of high-dose hyperthermic chemotherapy to the peritoneum. This therapeutic modality has been shown to benefit patients with peritoneal carcinomatosis resulting from gastrointestinal and ovarian tumors and mesothelioma. However, it is unknown whether the primary disease (mesothelioma versus peritoneal carcinomatosis) affects hemodynamic and metabolic perturbations during the course of CHPP with cisplatin. We examined the perioperative course of patients undergoing CHPP with cisplatin and evaluated the effect of primary diagnosis (mesothelioma versus peritoneal carcinomatosis) on hemodynamic and metabolic parameters in response to peritoneal perfusion. Sixty-nine mesothelioma and 100 peritoneal carcinomatosis patients underwent 169 consecutive cytoreduction and CHPP procedures with general anesthesia. During CHPP, patients from both groups developed significant increases in central venous pressure, and heart rate, decreases in mean arterial pressure (all <em>P</em> &#x0003c; 0.0001), metabolic acidosis with significant decreases in pH and bicarbonate (<em>P</em> &#x0003c; 0.0001), deterioration of gas exchange with significant increases in PaCO<sub>2</sub> and oxygen alveolar&#x02013;arterial gradient (<em>P</em> &#x0003c; 0.0001), and significant increases in activated partial thromboplastin time (aPTT) and prothrombin time (PT) and decreases in hematocrit and platelet counts (all <em>P</em> &#x0003c; 0.0001). However, patients with mesothelioma had lesser increases in temperature (<em>P</em> &#x0003c; 0.01) and heart rate (<em>P</em> &#x0003c; 0.0001) and lesser decreases in hematocrit (<em>P</em> = 0.0013) during CHPP and greater decreases in sodium bicarbonate (<em>P</em> = 0.0082) after completion of CHPP compared with patients with peritoneal carcinomatosis. We conclude that the transient hemodynamic and metabolic perturbations associated with cytoreductive surgery and CHPP with cisplatin can vary according to the primary diagnosis (mesothelioma versus peritoneal carcinomatosis) warranting this therapy.</p>
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		<title>Mesothelioma: treatment</title>
		<link>http://www.mesothelioma-line.com/articles/2008/11/26/other-thoracic-cancers-mesothelioma-treatment/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/11/26/other-thoracic-cancers-mesothelioma-treatment/#comments</comments>
		<pubDate>Wed, 26 Nov 2008 15:06:17 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Chemotherapy]]></category>
		<category><![CDATA[Cisplatin (Platinol ®)]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Pemetrexed (Alimta)]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Pleurectomy/decortication]]></category>
		<category><![CDATA[Pneumonectomy]]></category>
		<category><![CDATA[Radiation]]></category>
		<category><![CDATA[Raltitrexed (Tomudex)]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1547</guid>
		<description><![CDATA[Revue des Maladies Respiratoires. 2008 Oct;25(8 Pt 2):3S191-5. [Link] Berghmans T. Département des Soins Intensifs et Oncologie Thoracique, Institut Jules-Bordet (Centre des Tumeurs de l&#8217;Université Libre de Bruxelles), 1 Rue Héger-Bordet, Brussels, Belgium. thierry.berghmanns@bordet.be Abstract Malignant pleural mesothelioma is a rare tumour of poor prognosis. Available therapeutics have restricted efficacy. Pleuro-pneumonectomy is the only treatment [...]]]></description>
			<content:encoded><![CDATA[<p><em>Revue des Maladies Respiratoires.</em> 2008 Oct;25(8 Pt 2):3S191-5. [<a href="http://www.em-consulte.com/article/183841" target="_blank">Link</a>]</p>
<p><strong>Berghmans T.</strong></p>
<p>Département des Soins Intensifs et Oncologie Thoracique, Institut Jules-Bordet (Centre des Tumeurs de l&#8217;Université Libre de Bruxelles), 1 Rue Héger-Bordet, Brussels, Belgium. thierry.berghmanns@bordet.be</p>
<h3 class="abstract">Abstract</h3>
<p>Malignant pleural mesothelioma is a rare tumour of poor prognosis. Available therapeutics have restricted efficacy. Pleuro-pneumonectomy is the only treatment with curative intent but it could be offered to a limited and well selected group of patients. The role of radiotherapy is palliative and its preventive role on malignant seeding after invasive procedures is controversial. There are few active cytotoxic drugs in this disease. Currently, based on two randomised trials, the most efficacious chemotherapy regimen consists in a combination of cisplatin and an antifolate agent, pemetrexed or raltitrexed.</p>
<p><strong>Keywords:</strong> Mesothelioma, Surgery, Radiotherapy, Chemotherapy </p>
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		<title>Compensator-based intensity-modulated radiation therapy for malignant pleural mesothelioma post extrapleural pneumonectomy</title>
		<link>http://www.mesothelioma-line.com/articles/2008/11/21/compensator-based-intensity-modulated-radiation-therapy-for-malignant-pleural-mesothelioma-post-extrapleural-pneumonectomy/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/11/21/compensator-based-intensity-modulated-radiation-therapy-for-malignant-pleural-mesothelioma-post-extrapleural-pneumonectomy/#comments</comments>
		<pubDate>Fri, 21 Nov 2008 14:55:26 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Determining Efficacy]]></category>
		<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[IMRT]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Radiation]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1543</guid>
		<description><![CDATA[Journal of Applied Clinical Medical Physics. 2008 Oct 29;9(4):2799. [Link] Javedan K, Stevens CW, Forster K. Radiation Oncology,1 H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA. khosrow.javedan@moffitt.org Abstract The present work investigated the potential of compensator-based intensity-modulated radiation therapy (CB-IMRT) as an alternative to multileaf collimator (MLC)-based intensity-modulated radiation therapy (IMRT) to [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal of Applied Clinical Medical Physics.</em> 2008 Oct 29;9(4):2799. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/19020484?dopt=AbstractPlus" target="_blank">Link</a>]</p>
<p><strong>Javedan K, Stevens CW, Forster K.</strong></p>
<p>Radiation Oncology,1 H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, USA. khosrow.javedan@moffitt.org</p>
<h3 class="abstract">Abstract</h3>
<p>The present work investigated the potential of compensator-based intensity-modulated radiation therapy (CB-IMRT) as an alternative to multileaf collimator (MLC)-based intensity-modulated radiation therapy (IMRT) to treat malignant pleural mesothelioma (MPM) post extrapleural pneumonectomy. Treatment plans for 4 right-sided and 1 left-sided MPM post-surgery cases were generated using a commercial treatment planning system, XIO/CMS (Computerized Medical Systems, St. Louis, MO). We used a 7-gantry-angle arrangement with 6 MV beams to generate these plans. The maximum required field size was 30 x 40 cm. We evaluated IMRT plans with brass compensators (.Decimal, Sanford, FL) by examining isodose distributions, dose-volume histograms, metrics to quantify conformal plan quality, and homogeneity. Quality assurance was performed for one of the compensator plans. Conformal dose distributions were achieved with CB-IMRT for all 5 cases, the average planning target volume (PTV) coverage being 95.1% of the PTV volume receiving the full prescription dose. The average lung V20 (volume of lung receiving 20 Gy) was 1.8%, the mean lung dose was 6.7 Gy, and the average contralateral kidney V15 was 0.6%. The average liver dose V30 was 34.0% for the right-sided cases and 10% for the left-sided case. The average monitor units (MUs) per fraction were 980 MUs for the 45-Gy prescriptions (mean: 50 Gy) and 1083 MUs for the 50-Gy prescriptions (mean: 54 Gy). Post surgery, CB-IMRT for MPM is a feasible IMRT technique for treatment with a single isocenter. Compensator plans achieved dose objectives and were safely delivered on a Siemens Oncor machine (Siemens Medical Solutions, Malvern, PA). These plans showed acceptably conformal dose distributions as confirmed by multiple measurement techniques. Not all linear accelerators can deliver large-field MLC-based IMRT, but most can deliver a maximum conformal field of 40 x 40 cm. It is possible and reasonable to deliver IMRT with compensators for fields this size with most conventional linear accelerators.</p>
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