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DOI | 10.1016/j.jtho.2016.04.028 |
Consensus Report of the 2015 Weinman International Conference on Mesothelioma | |
Carbone, Michele1; Kanodia, Shreya1,2,3; Chao, Ann4; Miller, Aubrey5; Wali, Anil6; Weissman, David7; Adjei, Alex8; Baumann, Francine9; Boffetta, Paolo10; Buck, Brenda11; de Perrot, Marc12; Dogan, A. Umran13,14; Gavett, Steve15; Gualtieri, Alessandro16; Hassan, Raffit17; Hesdorffer, Mary18; Hirsch, Fred R.19; Larson, David1; Mao, Weimin20,21; Masten, Scott22; Pass, Harvey I.23; Peto, Julian24; Pira, Enrico25; Steele, Ian26; Tsao, Anne27; Woodard, Gavitt Alida28; Yang, Haining1; Malik, Shakun29 | |
发表日期 | 2016-08-01 |
ISSN | 1556-0864 |
卷号 | 11期号:8页码:1246-1262 |
英文摘要 | On November 9 and 10, 2015, the International Conference on Mesothelioma in Populations Exposed to Naturally Occurring Asbestiform Fibers was held at the University of Hawaii Cancer Center in Honolulu, Hawaii. The meeting was cosponsored by the International Association for the Study of Lung Cancer, and the agenda was designed with significant input from staff at the U.S. National Cancer Institute and National Institute of Environmental Health Sciences. A multidisciplinary group of participants presented updates reflecting a range of disciplinary perspectives, including mineralogy, geology, epidemiology, toxicology, biochemistry, molecular biology, genetics, public health, and clinical oncology. The group identified knowledge gaps that are barriers to preventing and treating malignant mesothelioma (MM) and the required next steps to address barriers. This manuscript reports the group's efforts and focus on strategies to limit risk to the population and reduce the incidence of MM. Four main topics were explored: genetic risk, environmental exposure, biomarkers, and clinical interventions. Genetics plays a critical role in MM when the disease occurs in carriers of germline BRCA1 associated protein 1 mutations. Moreover, it appears likely that, in addition to BRCA1 associated protein 1, other yet unknown genetic variants may also influence the individual risk for development of MM, especially after exposure to asbestos and related mineral fibers. MM is an almost entirely preventable malignancy as it is most often caused by exposure to commercial asbestos or mineral fibers with asbestos-like health effects, such as erionite. In the past in North America and in Europe, the most prominent source of exposure was related to occupation. Present regulations have reduced occupational exposure in these countries; however, some people continue to be exposed to previously installed asbestos in older construction and other settings. Moreover, an increasing number of people are being exposed in rural areas that contain noncommercial asbestos, erionite, and other mineral fibers in soil or rock (termed naturally occurring asbestos [NOA]) and are being developed. Public health authorities, scientists, residents, and other affected groups must work together in the areas where exposure to asbestos, including NOA, has been documented in the environment to mitigate or reduce this exposure. Although a blood biomarker validated to be effective for use in screening and identifying MM at an early stage in asbestos/NOA-exposed populations is not currently available, novel biomarkers presented at the meeting, such as high mobility group box 1 and fibulin-3, are promising. There was general agreement that current treatment for MM, which is based on surgery and standard chemotherapy, has a modest effect on the overall survival (OS), which remains dismal. Additionally, although much needed novel therapeutic approaches for MM are being developed and explored in clinical trials, there is a critical need to invest in prevention research, in which there is a great opportunity to reduce the incidence and mortality from MM. 2016 International Association for the Study of Lung Cancer. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
英文关键词 | Mesothelioma;BAP1;Asbestos;Erionite;Biomarkers;Genetics;Therapy |
语种 | 英语 |
WOS记录号 | WOS:000381067300008 |
来源期刊 | JOURNAL OF THORACIC ONCOLOGY
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来源机构 | 美国环保署 |
文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/62101 |
作者单位 | 1.Univ Hawaii, Thorac Oncol, Ctr Canc, Honolulu, HI 96822 USA; 2.Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Los Angeles, CA 90048 USA; 3.Cedars Sinai Med Ctr, Dept Biomed Sci, Los Angeles, CA 90048 USA; 4.NCI, Ctr Global Hlth, NIH, Bethesda, MD 20892 USA; 5.NIEHS, NIH, POB 12233, Res Triangle Pk, NC 27709 USA; 6.NCI, Ctr Reduce Canc Hlth Dispar, NIH, Bethesda, MD 20892 USA; 7.NIOSH, Resp Hlth Div, Ctr Dis Control & Prevent, Morgantown, WV USA; 8.Mayo Clin, Rochester, MN USA; 9.Univ New Caledonia, ERIM, Noumea, New Caledonia; 10.Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY USA; 11.Univ Nevada, Dept Geosci, Las Vegas, NV 89154 USA; 12.Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada; 13.Univ Iowa, Chem & Biochem Engn Dept, Iowa City, IA USA; 14.Univ Iowa, Ctr Global & Reg Environm Res, Iowa City, IA USA; 15.US EPA, Off Res & Dev, Res Triangle Pk, NC 27711 USA; 16.Univ Modena, Chem Earth Sci Dept, Modena, Italy; 17.NIH, Thorac Oncol Branch, Ctr Canc Res, Bldg 10, Bethesda, MD 20892 USA; 18.Mesothelioma Appl Res Fdn, Alexandria, VA USA; 19.Univ Colorado, Ctr Canc, Denver, CO 80202 USA; 20.Zhejiang Canc Hosp, Canc Res Inst, Hangzhou, Zhejiang, Peoples R China; 21.Key Lab Diag & Treatment Technol Thorac Oncol Zhe, Hangzhou, Zhejiang, Peoples R China; 22.NIEHS, Natl Toxicol Program, NIH, POB 12233, Res Triangle Pk, NC 27709 USA; 23.NYU, Langone Med Ctr, Cardiothorac Surg, New York, NY USA; 24.London Sch Hyg & Trop Med, Canc Res UK, London, England; 25.Univ Turin, Dept Publ Hlth & Pediat, Turin, Italy; 26.Notre Dame Univ, Notre Dame Integrated Imaging Facil, Notre Dame, IN USA; 27.Univ Texas MD Anderson Canc Ctr, Dept Thorac & Head & Neck Med Oncol, Div Canc Med, Houston, TX 77030 USA; 28.Univ Calif San Francisco, Thorac Surg, San Francisco, CA 94143 USA; 29.NCI, Canc Therapy Evaluat Program, NIH, Bethesda, MD 20892 USA |
推荐引用方式 GB/T 7714 | Carbone, Michele,Kanodia, Shreya,Chao, Ann,et al. Consensus Report of the 2015 Weinman International Conference on Mesothelioma[J]. 美国环保署,2016,11(8):1246-1262. |
APA | Carbone, Michele.,Kanodia, Shreya.,Chao, Ann.,Miller, Aubrey.,Wali, Anil.,...&Malik, Shakun.(2016).Consensus Report of the 2015 Weinman International Conference on Mesothelioma.JOURNAL OF THORACIC ONCOLOGY,11(8),1246-1262. |
MLA | Carbone, Michele,et al."Consensus Report of the 2015 Weinman International Conference on Mesothelioma".JOURNAL OF THORACIC ONCOLOGY 11.8(2016):1246-1262. |
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