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	<title>Mesothelioma Journal Articles &#187; Type of Assessment:</title>
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	<link>http://www.mesothelioma-line.com/articles</link>
	<description>Journal Articles on Mesothelioma: Cancer Information for Patients and Families</description>
	<pubDate>Thu, 13 Nov 2008 20:16:15 +0000</pubDate>
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	<language>en</language>
			<item>
		<title>The role of polio-vaccine in pleural mesothelioma&#8211;an epidemiological observation</title>
		<link>http://www.mesothelioma-line.com/articles/2008/09/02/the-role-of-polio-vaccine-in-pleural-mesothelioma-an-epidemiological-observation/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/09/02/the-role-of-polio-vaccine-in-pleural-mesothelioma-an-epidemiological-observation/#comments</comments>
		<pubDate>Tue, 02 Sep 2008 20:14:09 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Causation]]></category>

		<category><![CDATA[Epidemiological]]></category>

		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[Occupational Asbestos Exposure]]></category>

		<category><![CDATA[SV40]]></category>

		<category><![CDATA[Type of Assessment:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1352</guid>
		<description><![CDATA[Collegium Antropologicum.  2008 Jun;32(2):479-83.  [Link]
Sarić M, Curin K, Varnai VM.
Institute for Medical Research and Occupational Health, Zagreb, Croatia. marko@imi.hr
Abstract
From the Croatian Cancer Registry (period 1991-1997) 194 malignant pleural mesothelioma patients were collected. According to participation in polio vaccination mass campaign in 1961 that covered the entire Croatian population aged 3 months to 20 [...]]]></description>
			<content:encoded><![CDATA[<p><em>Collegium Antropologicum</em>.  2008 Jun;32(2):479-83.  [<a href="http://www.ncbi.nlm.nih.gov/pubmed/18756898?dopt=AbstractPlus" target="_blank">Link</a>]</p>
<p><strong>Sarić M, Curin K, Varnai VM.</strong></p>
<p>Institute for Medical Research and Occupational Health, Zagreb, Croatia. marko@imi.hr</p>
<h3 class="abstract">Abstract</h3>
<p>From the Croatian Cancer Registry (period 1991-1997) 194 malignant pleural mesothelioma patients were collected. According to participation in polio vaccination mass campaign in 1961 that covered the entire Croatian population aged 3 months to 20 years, mesothelioma patients were divided in vaccinated (N=58), and non-vaccinated (N=136) subjects. Significantly higher percentage of those with a history of occupational exposure to asbestos was found in vaccinated (79%) compared to non-vaccinated group (63%). This is the opposite to what would be expected if potential SV40 contamination of polio vaccine used had a causative role in the development of the tumour. On the other hand, shorter latency period reflected by very high percentage of 45-year-old or younger mesothelioma patients in vaccinated group (15 out of 58), with all of them having a history of occupational asbestos exposure, raises a question for a possible enhancing effect of the vaccine used to asbestos exposure, if it was contaminated with SV40.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>vaccine</dt><dd> the modified virus of a disease used to bring about resistance to that disease for a period of time, or even permanently. Development of a cancer vaccine is a subject of intense research.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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		</item>
		<item>
		<title>Malignant Pleural Mesothelioma–Targeted CREBBP/EP300 Inhibitory Protein 1 Promoter System for Gene Therapy and Virotherapy</title>
		<link>http://www.mesothelioma-line.com/articles/2008/09/02/malignant-pleural-mesothelioma%e2%80%93targeted-crebbpep300-inhibitory-protein-1-promoter-system-for-gene-therapy-and-virotherapy/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/09/02/malignant-pleural-mesothelioma%e2%80%93targeted-crebbpep300-inhibitory-protein-1-promoter-system-for-gene-therapy-and-virotherapy/#comments</comments>
		<pubDate>Tue, 02 Sep 2008 20:11:45 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[Gene Therapy]]></category>

		<category><![CDATA[New &#038; Novel]]></category>

		<category><![CDATA[Pleural]]></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=1350</guid>
		<description><![CDATA[Cancer Research.  2008 Sep 1;68(17):7120-9.  [Link]
Fukazawa T, Matsuoka J, Naomoto Y, Maeda Y, Durbin ML, Tanaka N.
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan. FukazawaT@aol.com
Abstract
Gene therapy and virotherapy are one of the approaches used to treat malignant pleural mesothelioma. To improve the efficiency of targeting [...]]]></description>
			<content:encoded><![CDATA[<p><em>Cancer Research</em>.  2008 Sep 1;68(17):7120-9.  [<a href="http://cancerres.aacrjournals.org/cgi/content/abstract/68/17/7120" target="_blank">Link</a>]</p>
<p><strong>Fukazawa T, Matsuoka J, Naomoto Y, Maeda Y, Durbin ML, Tanaka N.</strong></p>
<p>Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan. FukazawaT@aol.com</p>
<h3 class="abstract">Abstract</h3>
<p>Gene therapy and virotherapy are one of the approaches used to treat malignant pleural mesothelioma. To improve the efficiency of targeting malignant mesothelioma cells, we designed a novel system using the promoter of the CREBBP/EP300 inhibitory protein 1 (CRI1), a gene specifically expressed in malignant pleural mesothelioma. Four tandem repeats of the CRI1 promoter (CRI1(-138 4x)) caused significantly high promoter activity in malignant pleural mesothelioma cells but little promoter activity in normal mesothelial cells and normal fibroblasts. The recombinant adenoviral vector expressing proapoptotic BH3-interacting death agonist or early region 1A driven by the CRI1(-138 4x) promoter induced cell death in malignant mesothelioma cells but not in normal cells. Moreover, these viruses showed antitumor effects in a mesothelioma xenograft mouse model. Here, we describe a novel strategy to target malignant mesothelioma using the CRI1(-138 4x) promoter system.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>therapy</dt><dd> any of the measures taken to treat a disease. Unproven therapy is any therapy that has not been scientifically tested and approved. Use of an unproven therapy instead of standard (proven) therapy is called alternative therapy. Some alternative therapies have dangerous or even life-threatening side effects. For others, the main danger is that a patient may lose the opportunity to benefit from standard therapy. Complementary therapy, on the other hand, refers to therapies used in addition to standard therapy. Some complementary therapies may help relieve certain symptoms of cancer, relieve side effects of standard cancer therapy, or improve a patient's sense of well-being. The ACS recommends that patients considering use of any alternative or complementary therapy discuss this with their health care team.</dd><dt>gene therapy</dt><dd>a new type of treatment in which defective genes are replaced with normal ones. The new genes are delivered into the cells by viruses or proteins. (<a target="_blank" href="http://www.mesotheliomacenter.org/treatment/gene-therapy/">Mesothelioma gene therapy</a> treatment options.) </dd><dt>gene</dt><dd> a segment of DNA that contains information on hereditary characteristics such as hair color, eye color, and height, as well as susceptibility to certain diseases. Women who have BRCA1 or BRCA2 gene mutations (defects) have an inherited tendency to develop breast cancer.</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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		<title>Recent advances in the treatment of malignant pleural mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/09/02/recent-advances-in-the-treatment-of-malignant-pleural-mesothelioma/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/09/02/recent-advances-in-the-treatment-of-malignant-pleural-mesothelioma/#comments</comments>
		<pubDate>Tue, 02 Sep 2008 20:07:50 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Chemotherapy]]></category>

		<category><![CDATA[Cisplatin (Platinol ®)]]></category>

		<category><![CDATA[Determining Efficacy]]></category>

		<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>

		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[Gene Therapy]]></category>

		<category><![CDATA[Pemetrexed (Alimta)]]></category>

		<category><![CDATA[Pleural]]></category>

		<category><![CDATA[Pleurectomy/decortication]]></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=1348</guid>
		<description><![CDATA[Journal of Thoracic Oncology.  2008 Sep;3(9):1056-64.  [Link]
Ramalingam SS, Belani CP.
Emory University School of Medicine, Winship Cancer Institute, Atlanta, Georgia, USA.
Abstract
Malignant pleural mesothelioma clinically manifests after decades of initial exposure to etiologic agents, such as asbestos, and presents with nonspecific symptoms such as dyspnea, pain, or weight loss. In patients with limited, resectable disease, [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal of Thoracic Oncology</em>.  2008 Sep;3(9):1056-64.  [<a href="http://www.jto.org/pt/re/jto/abstract.01243894-200809000-00020.htm;jsessionid=JcJMKm1hLmvvS4JRtw5pKhpytvJqRZTHxRQ7BClfhlX0WfZ0mLyG!1571206638!181195629!8091!-1" target="_blank">Link</a>]</p>
<p><strong>Ramalingam SS, Belani CP.</strong></p>
<p>Emory University School of Medicine, Winship Cancer Institute, Atlanta, Georgia, USA.</p>
<h3 class="abstract">Abstract</h3>
<p><strong></strong>Malignant pleural mesothelioma clinically manifests after decades of initial exposure to etiologic agents, such as asbestos, and presents with nonspecific symptoms such as dyspnea, pain, or weight loss. In patients with limited, resectable disease, surgical therapy with extrapleural pneumonectomy or pleurectomy is recommended, although, it is unclear which approach is superior. Radiation has a limited role and is used primarily for palliation. The palliative efficacy of traditional chemotherapeutic agents and combination regimens is modest at best. The combination of cisplatin and pemetrexed, a novel multitargeted antifolate agent, is the approved &quot;standard of care&quot; for patients with unresectable malignant pleural mesothelioma. A number of molecularly targeted agents are currently under evaluation for mesothelioma such as the Histone deacetylase (HDAC) inhibitors that have demonstrated promising anticancer activity. Vorinostat, a small molecule inhibitor of HDAC, which targets select members of class I and II HDACs, has shown early evidence of activity and is currently being evaluated in a randomized study for patients who progress with standard therapy for advanced mesothelioma. It is hoped that the HDAC inhibitors and other novel targeted agents will pave the way for improved outcomes for patients with this disease.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>therapy</dt><dd> any of the measures taken to treat a disease. Unproven therapy is any therapy that has not been scientifically tested and approved. Use of an unproven therapy instead of standard (proven) therapy is called alternative therapy. Some alternative therapies have dangerous or even life-threatening side effects. For others, the main danger is that a patient may lose the opportunity to benefit from standard therapy. Complementary therapy, on the other hand, refers to therapies used in addition to standard therapy. Some complementary therapies may help relieve certain symptoms of cancer, relieve side effects of standard cancer therapy, or improve a patient's sense of well-being. The ACS recommends that patients considering use of any alternative or complementary therapy discuss this with their health care team.</dd><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>extrapleural pneumonectomy</dt><dd>(EPP) surgery to remove the pleura, diaphragm, pericardium, and entire lung involved with the tumor. You can view a web cast from <a title="Brigham & Women's Hospital web site opens in a new window." href="http://www.brighamandwomens.org/" target="_blank"><u>Brigham and Women's</u></a> Hospital in Boston of this procedure being done by Dr. David Sugarbaker: <a title="EPP web cast opens in a new window." href="http://www.or-live.com/BrighamandWomens/1108/" target="_parent"><u>see the extrapleural pneumonectomy (EPP) web cast here</u></a>. </dd><dt>pemetrexed</dt><dd>chemotheraputic agent that interferes with a crucial process that allows cancer cells to reproduce and spread. Specifically, pemetrexed stops the production of three enzymes that are required to feed the cancer cell. Often used in combination with cisplatin. Marketed under the name ALIMTA. See: <a href="/articles/glossary/?id=5">Alimta</a>. </dd></dl>]]></content:encoded>
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		<title>Diagnosis, Staging, and Surgical Treatment of Malignant Pleural Mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/09/02/diagnosis-staging-and-surgical-treatment-of-malignant-pleural-mesothelioma/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/09/02/diagnosis-staging-and-surgical-treatment-of-malignant-pleural-mesothelioma/#comments</comments>
		<pubDate>Tue, 02 Sep 2008 20:05:06 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Chemotherapy]]></category>

		<category><![CDATA[Determining Efficacy]]></category>

		<category><![CDATA[Diagnosis &#038; Differentiation]]></category>

		<category><![CDATA[Extrapleural Pneumonectomy (EPP)]]></category>

		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[Pleural]]></category>

		<category><![CDATA[Pleurectomy/decortication]]></category>

		<category><![CDATA[Staging]]></category>

		<category><![CDATA[Surgery]]></category>

		<category><![CDATA[Treatment]]></category>

		<category><![CDATA[Trimodality Therapy]]></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=1346</guid>
		<description><![CDATA[Current Treatment Options in Oncology. 2008 Jun;9(2-3):158-70. Epub 2008 Aug 29. [Link]
Kent M, Rice D, Flores R.
 Thoracic Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Abstract
Opinion statement: The clinical presentation of malignant pleural mesothelioma (MPM) is nonspecific. The process to obtain the correct diagnosis can be challenging and requires a [...]]]></description>
			<content:encoded><![CDATA[<p><em>Current Treatment Options in Oncology</em>. 2008 Jun;9(2-3):158-70. Epub 2008 Aug 29. [<a href="http://www.springerlink.com/content/3555946xr3846531/" target="_blank">Link</a>]</p>
<p><strong>Kent M, Rice D, Flores R.</strong></p>
<p> Thoracic Service, Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.</p>
<h3 class="abstract">Abstract</h3>
<p><strong>Opinion statement</strong>: The clinical presentation of malignant pleural mesothelioma (MPM) is nonspecific. The process to obtain the correct diagnosis can be challenging and requires a high index of suspicion. Once the diagnosis is made, there is no universally accepted standard of care and treatment decisions are strongly influenced by physician bias. Physicians who see few numbers of patients tend to treat based on symptoms alone by drainage of the pleural effusion and talc pleurodesis, while physicians at several tertiary referral centers tend to take an aggressive multimodality approach incorporating surgical resection, chemotherapy, and radiation. The primary goal of surgery in this setting is the resection of all gross disease. The choice of operation, extrapleural pneumonectomy (EPP) or pleurectomy/decortication (P/D), depends on disease stage, pulmonary function, philosophy of the treating physician, and type of planned adjuvant therapy.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>adjuvant therapy</dt><dd><span class="pronunciation">(add-joo-vunt)</span> treatment used in addition to the main treatment. It usually refers to hormonal therapy, chemotherapy, or radiation added after surgery to increase the chances of curing the disease or keeping it in check.</dd><dt>therapy</dt><dd> any of the measures taken to treat a disease. Unproven therapy is any therapy that has not been scientifically tested and approved. Use of an unproven therapy instead of standard (proven) therapy is called alternative therapy. Some alternative therapies have dangerous or even life-threatening side effects. For others, the main danger is that a patient may lose the opportunity to benefit from standard therapy. Complementary therapy, on the other hand, refers to therapies used in addition to standard therapy. Some complementary therapies may help relieve certain symptoms of cancer, relieve side effects of standard cancer therapy, or improve a patient's sense of well-being. The ACS recommends that patients considering use of any alternative or complementary therapy discuss this with their health care team.</dd><dt>resection</dt><dd> surgery to remove part or all of an organ or other structure.</dd><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>diagnosis</dt><dd> identifying a disease by its signs or symptoms, and by using imaging procedures and laboratory findings. The earlier a diagnosis of cancer is made, the better the chance for long-term survival.</dd><dt>chemotherapy</dt><dd><span class="pronunciation">(key-mo-THER-uh-pee)</span> treatment with drugs to destroy cancer cells. Chemotherapy is often used with surgery or radiation to treat cancer when the cancer has spread, when it has come back (recurred), or when there is a strong chance that it could recur.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>extrapleural pneumonectomy</dt><dd>(EPP) surgery to remove the pleura, diaphragm, pericardium, and entire lung involved with the tumor. You can view a web cast from <a title="Brigham & Women's Hospital web site opens in a new window." href="http://www.brighamandwomens.org/" target="_blank"><u>Brigham and Women's</u></a> Hospital in Boston of this procedure being done by Dr. David Sugarbaker: <a title="EPP web cast opens in a new window." href="http://www.or-live.com/BrighamandWomens/1108/" target="_parent"><u>see the extrapleural pneumonectomy (EPP) web cast here</u></a>. </dd><dt>pleural effusion</dt><dd>an abnormal accumulation of fluid, usually caused by trauma or disease, in the pleural space.</dd></dl>]]></content:encoded>
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		<title>Stathmin 1: a novel therapeutic target for anticancer activity</title>
		<link>http://www.mesothelioma-line.com/articles/2008/09/02/stathmin-1-a-novel-therapeutic-target-for-anticancer-activity/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/09/02/stathmin-1-a-novel-therapeutic-target-for-anticancer-activity/#comments</comments>
		<pubDate>Tue, 02 Sep 2008 20:03:38 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[New &#038; Novel]]></category>

		<category><![CDATA[Treatment]]></category>

		<category><![CDATA[Type of Assessment:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1344</guid>
		<description><![CDATA[Expert Review of Anticancer Therapy. 2008 Sep;8(9):1461-70. [Link]
Rana S, Maples PB, Senzer N, Nemunaitis J.
 Gradalis, Inc., 2545 Golden Bear Drive, Suite 110, Carrollton, TX 75006, USA. srana@gradalisinc.com
Abstract
 Stathmin 1 (STMN1), also known as p17, p18, p19, 19K, metablastin, oncoprotein 18, LAP 18 and Op18, is a 19 kDa cytosolic protein. It was the first [...]]]></description>
			<content:encoded><![CDATA[<p><em>Expert Review of Anticancer Therapy</em>. 2008 Sep;8(9):1461-70. [<a href="http://www.expert-reviews.com/doi/abs/10.1586/14737140.8.9.1461?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub%3dncbi.nlm.nih.gov" target="_blank">Link</a>]</p>
<p><strong>Rana S, Maples PB, Senzer N, Nemunaitis J.</strong></p>
<p> Gradalis, Inc., 2545 Golden Bear Drive, Suite 110, Carrollton, TX 75006, USA. srana@gradalisinc.com</p>
<h3 class="abstract">Abstract</h3>
<p> Stathmin 1 (STMN1), also known as p17, p18, p19, 19K, metablastin, oncoprotein 18, LAP 18 and Op18, is a 19 kDa cytosolic protein. It was the first discovered member of a family of phylogenetically related microtubule-destabilizing phosphoproteins critically involved in the construction and function of the mitotic spindle. A threshold level of STMN1 is required for orderly progression through mitosis in a variety of cell types. STMN1 is overexpressed across a broad range of human malignancies (leukemia, lymphoma, neuroblastoma; ovarian, prostatic, breast and lung cancers and mesothelioma). It is also upregulated in normally proliferating cell lines but is only rarely upregulated in nonproliferating cell lines with the exception of neurons, anterior pituitary cells and glial cells. Its expression is also upregulated in hepatocytes during regeneration and in lymphoid cells when they are signaled to proliferate. In this review, we summarize available data as rationale for the therapeutic manipulation of STMN1 in cancer patients.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>therapy</dt><dd> any of the measures taken to treat a disease. Unproven therapy is any therapy that has not been scientifically tested and approved. Use of an unproven therapy instead of standard (proven) therapy is called alternative therapy. Some alternative therapies have dangerous or even life-threatening side effects. For others, the main danger is that a patient may lose the opportunity to benefit from standard therapy. Complementary therapy, on the other hand, refers to therapies used in addition to standard therapy. Some complementary therapies may help relieve certain symptoms of cancer, relieve side effects of standard cancer therapy, or improve a patient's sense of well-being. The ACS recommends that patients considering use of any alternative or complementary therapy discuss this with their health care team.</dd><dt>lymphoma</dt><dd><span class="pronunciation">(lim-foam-uh)</span> a cancer of the lymphatic system, a network of thin vessels and nodes throughout the body. Its function is to fight infection. Lymphoma involves a type of white blood cells called lymphocytes. The two main types of lymphoma are Hodgkin's disease and non-Hodgkin's lymphoma. The treatment methods for these two types of lymphomas are very different.</dd><dt>leukemia</dt><dd><span class="pronunciation">(loo-key-me-uh) </span>cancer of the blood or blood-forming organs. People with leukemia often have a noticeable increase in white blood cells (leukocytes).</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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		<title>YAP1 is involved in mesothelioma development and negatively regulated by Merlin through phosphorylation</title>
		<link>http://www.mesothelioma-line.com/articles/2008/08/30/yap1-is-involved-in-mesothelioma-development-and-negatively-regulated-by-merlin-through-phosphorylation/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/08/30/yap1-is-involved-in-mesothelioma-development-and-negatively-regulated-by-merlin-through-phosphorylation/#comments</comments>
		<pubDate>Sat, 30 Aug 2008 17:27:40 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[Gene Therapy]]></category>

		<category><![CDATA[New &#038; Novel]]></category>

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		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1342</guid>
		<description><![CDATA[Carcinogenesis. 2008 Nov;29(11):2139-46. Epub 2008 Aug 25. [Link]
Yokoyama T, Osada H, Murakami H, Tatematsu Y, Taniguchi T, Kondo Y, Yatabe Y, Hasegawa Y, Shimokata K, Horio Y, Hida T, Sekido Y.
Division of Molecular Oncology, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan.
Abstract
 We previously reported the results of bacterial artificial chromosome array [...]]]></description>
			<content:encoded><![CDATA[<p><em>Carcinogenesis</em>. 2008 Nov;29(11):2139-46. Epub 2008 Aug 25. [<a href="http://carcin.oxfordjournals.org/cgi/content/abstract/29/11/2139" target="_blank">Link]</a></p>
<p><strong>Yokoyama T, Osada H, Murakami H, Tatematsu Y, Taniguchi T, Kondo Y, Yatabe Y, Hasegawa Y, Shimokata K, Horio Y, Hida T, Sekido Y.</strong></p>
<p>Division of Molecular Oncology, Aichi Cancer Center Research Institute, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan.</p>
<h3 class="abstract">Abstract</h3>
<p> We previously reported the results of bacterial artificial chromosome array comprehensive genomic hybridization of malignant pleural mesotheliomas (MPMs), including two cases with high-level amplification in the 11q22 locus. In this study, we found that the <em>YAP1</em> gene encoding a transcriptional coactivator was localized in this amplified region and overexpressed in both cases, suggesting it as a candidate oncogene in this region. We analyzed the involvement of YAP1 in MPM proliferation, as well as its functional and physical interaction with Merlin encoded by the <em>neurofibromatosis type 2</em> (<em>NF2</em>) tumor suppressor gene, which is frequently mutated in MPMs. YAP1-RNA interference suppressed growth of a mesothelioma cell line NCI-H290 with <em>NF2</em> homozygous deletion, probably through cell-cycle arrest and apoptosis induction, whereas YAP1 transfection promoted the growth of MeT-5A, an immortalized mesothelial cell line. We also found that the introduction of <em>NF2</em> into NCI-H290 induced phosphorylation at serine 127 of YAP1, which was accompanied by reduction of nuclear localization of YAP1, whereas nuclear localization of a YAP1 S 127A mutant was not affected. Furthermore, results of immunoprecipitation and <em>in vitro</em> pull-down assays indicated a physical interaction between Merlin and YAP1. These results suggest that YAP1 is involved in mesothelial cell growth and that the transcriptional coactivator activity of YAP1 is functionally inhibited by Merlin through the induction of phosphorylation and cytoplasmic retention of YAP1. This is the first report of negative regulatory signaling from Merlin to YAP1 in mammalian cells. Future studies of transcriptional targets of YAP1 in MPMs may shed light on the molecular mechanisms of MPM development and lead to new therapeutic strategies. </p>
<p><strong>Abbreviations:</strong> BAC, bacterial artificial chromosome; CGH, comprehensive genomic hybridization; EGFP, enhanced green fluorescent protein; GST, glutathione S-transferase; MPM, malignant pleural mesothelioma; NF2, neurofibromatosis type 2; NHERF1, Na(+)/H(+) exchanger regulatory factor 1; PCR, polymerase chain reaction; RNAi, RNA interference; SDS, sodium dodecyl sulfate; sh, short hairpin</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>oncogene</dt><dd><span class="pronunciation">(on-ko-gene)</span> a type of gene. Normally inactive, when these genes are &quot;turned on&quot; (activated), they cause normal cells to change into cancer cells.</dd><dt>gene</dt><dd> a segment of DNA that contains information on hereditary characteristics such as hair color, eye color, and height, as well as susceptibility to certain diseases. Women who have BRCA1 or BRCA2 gene mutations (defects) have an inherited tendency to develop breast cancer.</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>tumor</dt><dd> an abnormal lump or mass of tissue. Tumors can be benign (not cancerous) or malignant (cancerous).</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>apoptosis</dt><dd>a type of cell death in which the cell basically commits suicide; scientists believe some types of cancer may originate from an interruption of this programmed cell death, allowing cells to grow out of control.</dd></dl>]]></content:encoded>
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		<title>Technical aspects of cytoreductive surgery</title>
		<link>http://www.mesothelioma-line.com/articles/2008/08/30/technical-aspects-of-cytoreductive-surgery/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/08/30/technical-aspects-of-cytoreductive-surgery/#comments</comments>
		<pubDate>Sat, 30 Aug 2008 17:24:50 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Determining Efficacy]]></category>

		<category><![CDATA[Full Archive]]></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=1340</guid>
		<description><![CDATA[Journal of Surgical Oncology. 2008 Sep 15;98(4):232-6. [Link]
Kusamura S, O&#8217;Dwyer ST, Baratti D, Younan R, Deraco M.
Department of Surgery, National Cancer Institute of Milan, Milan, Italy.
Abstract
  At the Fifth International Workshop on Peritoneal Surface Malignancy, in Milan, the consensus on technical aspects of cytoreductive surgery (CRS) for peritoneal surface malignancy was obtained through the [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal of Surgical Oncology</em>. 2008 Sep 15;98(4):232-6. [<a href="http://www3.interscience.wiley.com/journal/121384696/abstract" target="_blank">Link]</a></p>
<p><strong>Kusamura S, O&#8217;Dwyer ST, Baratti D, Younan R, Deraco M.</strong></p>
<p>Department of Surgery, National Cancer Institute of Milan, Milan, Italy.</p>
<h3 class="abstract">Abstract</h3>
<p>  At the Fifth International Workshop on Peritoneal Surface Malignancy, in Milan, the consensus on technical aspects of cytoreductive surgery (CRS) for peritoneal surface malignancy was obtained through the Delphi process. Five conflicting points were discussed: radicality of the peritonectomy procedure, cytoreduction of neoplastic nodules &lt;2.5 mm, the timing of bowel anastomoses in relation to hyperthermic intraperitoneal chemotherapy (HIPEC) and indications of protective ostomies. According to the panel of experts a partial parietal peritonectomy restricted to the macroscopically involved regions could be indicated in all listed clinical conditions with the exception of peritoneal mesothelioma. No expert was of the opinion that a radical parietal peritonectomy is advisable irrespective of the disease being treated. All the experts agreed that electrovaporization of small (&lt;2.5 mm) non-infiltrating metastatic nodules in the mesentery would be appropriate, even if theoretically<br />
the HIPEC affords microscopic cytoreduction. The panel also agreed that in the closed technique for HIPEC administration the intestinal anastomoses should be fashioned after completion of the perfusion. Finally when considering the place for protective ostomies the experts voted for a flexible approach allowing the surgeon to exercise discretion for individual patients.</p>
<p><strong>Keywords</strong>: peritoneal carcinomatosis, cytoreductive surgery, consensus</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>chemotherapy</dt><dd><span class="pronunciation">(key-mo-THER-uh-pee)</span> treatment with drugs to destroy cancer cells. Chemotherapy is often used with surgery or radiation to treat cancer when the cancer has spread, when it has come back (recurred), or when there is a strong chance that it could recur.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd><dt>intraperitoneal chemotherapy</dt><dd>(IPC) a form of regional chemotherapy; the flooding of the abdominal cavity with chemotheraputic drugs to target the cancer cells directly.  It is sometimes heated to improve absorption of the anticancer drugs by the cancerous cells and because heat itself can kill cancer cells. </dd></dl>]]></content:encoded>
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		<title>The Fifth International Workshop on Peritoneal Surface Malignancy (Milan, Italy, December 4-6, 2006): methodology of disease-specific consensus</title>
		<link>http://www.mesothelioma-line.com/articles/2008/08/30/the-fifth-international-workshop-on-peritoneal-surface-malignancy-milan-italy-december-4-6-2006-methodology-of-disease-specific-consensus/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/08/30/the-fifth-international-workshop-on-peritoneal-surface-malignancy-milan-italy-december-4-6-2006-methodology-of-disease-specific-consensus/#comments</comments>
		<pubDate>Sat, 30 Aug 2008 17:21:54 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Full Archive]]></category>

		<category><![CDATA[General]]></category>

		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>

		<category><![CDATA[Type of Assessment:]]></category>

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		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1338</guid>
		<description><![CDATA[Journal of Surgical Oncology. 2008 Sep 15;98(4):258-62. [Link]
Baratti D, Kusamura S, Deraco M.
Department of Surgery, National Cancer Institute, Milan, Italy.
Abstract
  Peritoneal surface malignancies (PSM) have been traditionally regarded as uniformly terminal conditions. The combination of cyto-reductive surgery and perioperative intraperitoneal chemotherapy has changed PSM management from palliation to possible cure. Due to the inherent [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal of Surgical Oncology</em>. 2008 Sep 15;98(4):258-62. [<a href="http://www3.interscience.wiley.com/journal/121384742/abstract" target="_blank">Link]</a></p>
<p><strong>Baratti D, Kusamura S, Deraco M.</strong></p>
<p>Department of Surgery, National Cancer Institute, Milan, Italy.</p>
<h3 class="abstract">Abstract</h3>
<p>  Peritoneal surface malignancies (PSM) have been traditionally regarded as uniformly terminal conditions. The combination of cyto-reductive surgery and perioperative intraperitoneal chemotherapy has changed PSM management from palliation to possible cure. Due to the inherent differences in biological and clinical behavior, the optimal adaptation of comprehensive treatment to each PSM is still a matter of debate. A session of The Fifth International Workshop on Peritoneal Surface Malignancy (Milan, Italy, December 4-6, 2006) was committed to reach a consensus pertaining to conceptual and technical aspects of the loco-regional treatment of each PSM. The consensus developing process was based on principles of the Delphi method. A total of 103 international experts from 17 countries were included in six Working Groups (WG) for each of the following PSM: peritoneal mesothelioma, abdominal sarcomatosis, carcinomatosis of gastric, colo-rectal, appendiceal, and ovarian origin. Evidence reports were written by the respective WG. The main conflicting points (CP) regarding preoperative evaluation, patient eligibility, combined treatment methodology, postoperative follow-up and future investigational perspectives were summarized as a list of multiple-choice questions. Overall, 160 CP were identified. A consensus 51% of voters favoring one option was reached in 143/160 CP (89.4%). The general treatment guidelines and future investigational perspectives were defined.</p>
<p><strong>Keywords</strong>: consensus, peritoneal surface malignancies, cytoreductive surgery, hyperthermic intraperitoneal chemotherapy, HIPEC</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>chemotherapy</dt><dd><span class="pronunciation">(key-mo-THER-uh-pee)</span> treatment with drugs to destroy cancer cells. Chemotherapy is often used with surgery or radiation to treat cancer when the cancer has spread, when it has come back (recurred), or when there is a strong chance that it could recur.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd><dt>intraperitoneal chemotherapy</dt><dd>(IPC) a form of regional chemotherapy; the flooding of the abdominal cavity with chemotheraputic drugs to target the cancer cells directly.  It is sometimes heated to improve absorption of the anticancer drugs by the cancerous cells and because heat itself can kill cancer cells. </dd></dl>]]></content:encoded>
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		<title>Consensus statement on peritoneal mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/08/30/consensus-statement-on-peritoneal-mesothelioma/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/08/30/consensus-statement-on-peritoneal-mesothelioma/#comments</comments>
		<pubDate>Sat, 30 Aug 2008 17:18:56 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Chemotherapy]]></category>

		<category><![CDATA[Determining Efficacy]]></category>

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		<category><![CDATA[Intraperitoneal Chemotherapy]]></category>

		<category><![CDATA[Surgery]]></category>

		<category><![CDATA[Treatment]]></category>

		<category><![CDATA[Tumor Debulking]]></category>

		<category><![CDATA[Type of Assessment:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1336</guid>
		<description><![CDATA[Journal of Surgical Oncology. 2008 Sep 15;98(4):268-72. [Link]
Deraco M, Bartlett D, Kusamura S, Baratti D.
Department of Surgery, National Cancer Institute, Milan, Italy. marcello.deraco@istitutotumori.mi.it
Abstract
Diffuse malignant peritoneal mesothelioma (DMPM) has been traditionally regarded as a rapidly lethal disease. Recently, several independent prospective trials have reported improved survival with an intensive loco-regional treatment strategy including cytoreductive surgery (CRS) [...]]]></description>
			<content:encoded><![CDATA[<p><em>Journal of Surgical Oncology</em>. 2008 Sep 15;98(4):268-72. [<a href="http://www3.interscience.wiley.com/journal/121384759/abstract" target="_blank">Link]</a></p>
<p><strong>Deraco M, Bartlett D, Kusamura S, Baratti D.</strong></p>
<p>Department of Surgery, National Cancer Institute, Milan, Italy. marcello.deraco@istitutotumori.mi.it</p>
<h3 class="abstract">Abstract</h3>
<p>Diffuse malignant peritoneal mesothelioma (DMPM) has been traditionally regarded as a rapidly lethal disease. Recently, several independent prospective trials have reported improved survival with an intensive loco-regional treatment strategy including cytoreductive surgery (CRS) along with peri-operative intra-peritoneal chemotherapy (PIC). However, most of the surgical data comes from mono-institutional phase I or II studies and there is a broad range of variability regarding inclusion criteria, cytoreductive surgical procedures, drugs, temperatures and methods of delivering the heated chemotherapy (open vs. closed abdomen). This manuscript critically analyze and discuss the results of a group of health care providers trying to achieve a consensus statement in the management of this group of patients. The main conflicting points regarding preoperative evaluation, patient eligibility, combined treatment methodology, postoperative follow-up and future investigational perspectives were summarized as a list of multiple-choice questions. A questionnaire was placed on the website of the &#8220;5<sup>th<sup> International Workshop on Peritoneal Surface Malignancies&#8221; and the group members voted via internet. The results were presented for further debate during a dedicated session of the Workshop. The general treatment guidelines and future investigational perspectives were defined.</p>
<p>Keywords: consensus, peritoneal mesothelioma, cytoreductive surgery, hyperthermic intra-peritoneal chemotherapy, HIPEC</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>chemotherapy</dt><dd><span class="pronunciation">(key-mo-THER-uh-pee)</span> treatment with drugs to destroy cancer cells. Chemotherapy is often used with surgery or radiation to treat cancer when the cancer has spread, when it has come back (recurred), or when there is a strong chance that it could recur.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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		<title>Occupational exposure to asbestos and mortality among asbestos removal workers: a Poisson regression analysis</title>
		<link>http://www.mesothelioma-line.com/articles/2008/08/30/occupational-exposure-to-asbestos-and-mortality-among-asbestos-removal-workers-a-poisson-regression-analysis/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/08/30/occupational-exposure-to-asbestos-and-mortality-among-asbestos-removal-workers-a-poisson-regression-analysis/#comments</comments>
		<pubDate>Sat, 30 Aug 2008 17:16:57 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
		
		<category><![CDATA[Causation]]></category>

		<category><![CDATA[Epidemiological]]></category>

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		<category><![CDATA[Occupational Asbestos Exposure]]></category>

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		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1334</guid>
		<description><![CDATA[British Journal of Cancer. 2008 Sep 2;99(5):822-9. Epub 2008 Aug 19. [Link]
Frost G, Harding AH, Darnton A, McElvenny D, Morgan D.
Health &#38; Safety Laboratory, Harpur Hill, Buxton, Derbyshire SK17 9JN, UK. Gillian.Frost@hsl.gov.uk
Abstract
The asbestos industry has shifted from manufacture to stripping/removal work. The aim of this study was to investigate early indications of mortality among removal [...]]]></description>
			<content:encoded><![CDATA[<p><em>British Journal of Cancer</em>. 2008 Sep 2;99(5):822-9. Epub 2008 Aug 19. [<a href="http://www.nature.com/bjc/journal/v99/n5/abs/6604564a.html" target="_blank">Link]</a></p>
<p><strong>Frost G, Harding AH, Darnton A, McElvenny D, Morgan D.</strong></p>
<p>Health &amp; Safety Laboratory, Harpur Hill, Buxton, Derbyshire SK17 9JN, UK. Gillian.Frost@hsl.gov.uk</p>
<h3 class="abstract">Abstract</h3>
<p>The asbestos industry has shifted from manufacture to stripping/removal work. The aim of this study was to investigate early indications of mortality among removal workers. The study population consisted of 31 302 stripping/removal workers in the Great Britain Asbestos Survey, followed up to December 2005. Relative risks (RR) for causes of death with elevated standardised mortality ratios (SMR) and sufficient deaths were obtained from Poisson regression. Risk factors considered included dust suppression technique, type of respirator used, hours spent stripping, smoking status and exposure length. Deaths were elevated for all causes (SMR 123, 95% CI 119-127, n=985), all cancers including lung cancer, mesothelioma, and circulatory disease. There were no significant differences between suppression techniques and respirator types. Spending more than 40 h per week stripping rather than less than 10, increased mortality risk from all causes (RR 1.4, 95% CI 1.2-1.7), circulatory disease and ischaemic heart disease. Elevated mesothelioma risks were observed for those first exposed at young ages or exposed for more than 30 years. This study is a first step in assessing long-term mortality of asbestos removal workers in relation to working practices and asbestos exposure. Further follow-up will allow the impact of recent regulations to be assessed.</p>
<p><strong>Keywords</strong>: asbestos, mortality, Great Britain, occupational exposure, asbestos removal</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>mortality</dt><dd> a measure of the rate of death from a disease within a given population.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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